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other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. 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The main objectives of the journal include: providing an intellectual platform for Vietnamese and international scholars; promoting interdisciplinary studies in social sciences and humanities; becoming the leading journal in social sciences and humanities in Vietnam; being indexed by worldwide databases and having academic recognition internationally in the near future.\\nThe journal is currently indexed by Google Scholar, WorldCat, Open Archives, Cosmos Impact Factor, Advanced Sciences Index, Scientific Indexing Services, CrossRef, EBSCO Information Services and Vietnam National University’s digital archive.\\n\"},{\"attributes\":{\"bold\":true},\"insert\":\"Journal of Social Sciences and Humanities-Vietnam\"},{\"insert\":\"\\n\"},{\"attributes\":{\"bold\":true},\"insert\":\"ISSN 2354-1172, email: tapchikhxhnv@gmail.com, tckhxhnv@vnu.edu.vn\"},{\"insert\":\"\\n\"}]}","{\"ops\":[{\"insert\":\"Được thành lập ngày 31\u002F8\u002F2015 (giấy phép hoạt động số 155\u002FGP-BVHTT ngày 11 tháng 5 năm 2015 của Bộ Thông tin và Truyền thông, mã số tiêu chuẩn quốc tế ISSN 2354-1172), Tạp chí Khoa học Xã hội và Nhân văn (Journal of Social Sciences and Humanities) là ấn phẩm khoa học chính thức, duy nhất của Trường Đại học Khoa học Xã hội và Nhân văn, ĐHQG Hà Nội, phát triển và kế thừa Chuyên san Khoa học Xã hội và Nhân văn, Tạp chí Khoa học, ĐHQG Hà Nội.\\nTạp chí xuất bản định kỳ (04 số tiếng Việt\u002Fnăm và 02 số tiếng Anh\u002Fnăm), có nhiệm vụ \"},{\"attributes\":{\"italic\":true},\"insert\":\"công bố, giới thiệu các công trình nghiên cứu khoa học khoa học xã hội và nhân văn của các tác giả là các nhà khoa học trong và ngoài nước, phục vụ giảng dạy, học tập và nghiên cứu khoa học\"},{\"insert\":\". Hội đồng biên tập của Tạp chí hiện bao gồm 33 nhà khoa học có uy tín trong nước và quốc tế. Tạp chí tập trung và ưu tiên đăng tải những bài báo theo định hướng của tinh thần cởi mở, sáng tạo, nhanh chóng vươn lên để tiếp cận và sánh ngang với các tạp chí có uy tín hàng đầu của khu vực và trên thế giới. Nội dung chính của Tạp chí bao gồm các Bài nghiên cứu (khoảng 6000 đến 15000 từ), các bài điểm sách, thông tin khoa học (khoảng 300 đến 1500 từ) được trình bày theo đúng cấu trúc và chuẩn mực của một tạp chí khoa học.\\nCác bài viết của Tạp chí hiện đang được trích dẫn bởi Google Scholar, WorldCat, Open Archives, Cosmos Impact Factor, Advanced Sciences Index, Scientific Indexing Services, CrossRef, EBSCO Information Services.\\nMọi thông tin xin liên hệ: \"},{\"attributes\":{\"italic\":true},\"insert\":\"Phòng Tạp chí, 701 - E, Trường Đại học Khoa học Xã hội và Nhân văn, 336 Nguyễn Trãi, Thanh Xuân, Hà Nội. 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And the first issue was published in January 1998 with ISSN 1859-0128. Since then, STDJ has become the most important scientific forum of scientists from VNU-HCM as well as other universities. The magazine has undergone 20 years of development and has become a bridge for scientific exchanges, as well as enriching reference materials for the faculty, doctoral students, students of VNU-HCM in particular and other universities, institutes...\"},{\"attributes\":{\"align\":\"justify\"},\"insert\":\"\\n\"},{\"insert\":\"Science and Technology Development Journal - Health Sciences (STDJ-HS) is a subjournal of Science and Technology Development Journal since 2020.\"},{\"attributes\":{\"align\":\"justify\"},\"insert\":\"\\n\"},{\"insert\":\" \"},{\"attributes\":{\"align\":\"justify\"},\"insert\":\"\\n\"},{\"attributes\":{\"bold\":true},\"insert\":\"2. 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Central to this process is the endogenous mesenchymal stem cell (MSC), which coordinates the repair response by recruiting other host cells and secreting growth factors and matrix proteins. MSCs are self-renewing multipotent stem cells that can differentiate into various lineages of mesenchymal origin such as bone, cartilage, tendon, and fat. In addition to multilineage differentiation capacity, MSCs regulate immune response and inflammation and possess powerful tissue protective and reparative mechanisms, making these cells attractive for treatment of different diseases. The beneficial effect of exogenous MSCs on wound healing was observed in a variety of animal models and in reported clinical cases. Specifically, they have been successfully used to treat chronic wounds and stimulate stalled healing processes. Recent studies revealed that human placental membranes are a rich source of MSCs for tissue regeneration and repair. 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MSC là những tế bào gốc đa năng có khả năng tự phục hồi, có thể biệt hóa thành nhiều loại tế bào có nguồn gốc trung mô khác nhau như xương, sụn, gân và mỡ. Ngoài khả năng biệt hóa đa dòng, MSC còn điều hòa phản ứng miễn dịch và viêm, đồng thời sở hữu các cơ chế bảo vệ và sửa chữa mô mạnh mẽ, khiến cho các tế bào này trở nên hấp dẫn cho việc điều trị nhiều bệnh lý khác nhau. Hiệu quả tích cực của MSC ngoại sinh trong việc hồi phục vết thương đã được quan sát thấy ở nhiều mô hình động vật và trong các trường hợp lâm sàng đã được báo cáo. Cụ thể, chúng đã được sử dụng thành công để điều trị các vết thương mạn tính và kích thích các quá trình lành lại đã bị ngưng trệ. Các nghiên cứu gần đây đã phát hiện ra rằng màng nhau thai người là nguồn giàu MSC cho việc tái tạo và sửa chữa mô. Bài tổng quan này cung cấp một tóm tắt ngắn gọn về những hiểu biết hiện tại về các thuộc tính sinh học của MSC và mô tả việc sử dụng MSC trong hồi phục vết thương. Đặc biệt, phạm vi của bài tổng quan này tập trung vào vai trò của MSC trong từng giai đoạn của quá trình hồi phục vết thương. Ngoài ra, sự đặc trưng của MSC chứa tế bào thay thế da cũng được mô tả, cho thấy sự hiện diện của các yếu tố tăng trưởng và cytokine chủ chốt đặc biệt phù hợp để hỗ trợ trong việc sửa chữa vết thương.\u003C\u002Fjats:p>",{"EN":786,"VI":787},"Concise Review: Role of Mesenchymal Stem Cells in Wound Repair","Tổng quan ngắn gọn: Vai trò của tế bào gốc trung mô trong quá trình phục hồi vết thương",{"VOID":789},"23197761",{"VOID":791},"10.5966\u002Fsctm.2011-0018","PUBLICATION","Auto Verify",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F1\u002F2\u002F142-149\u002F6386961",[798,817,832,847,862],{"id":799,"sortIndex":115,"researcher":26,"roles":800,"affiliations":801,"properties":812},"4333a5cf-aa79-475e-ba62-018c16a886b3",[],[802],{"id":803,"sortIndex":36,"affiliation":804,"properties":26},"9369b652-3d05-489d-8737-142bc42cb11f",{"id":805,"createTime":806,"updateTime":806,"relativeEntities":807,"slug":808,"properties":809,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"a95bb45a-0423-4354-bbf4-f04fbb0f4461","2024-10-16T03:17:51.029+00:00",[],"Osiris-Therapeutics-Inc-Columbia-Maryland-USA",{"title":810},{"EN":811},"Osiris Therapeutics, Inc., Columbia, Maryland, USA",{"openalex":813,"title":815},{"VOID":814},"A5053029409",{"EN":816},"Erasmo A. 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10.1097\u002FBCR.0b013e31818b9e40",{"doi":1154},"10.1097\u002FBCR.0b013e31818b9e40",{"id":26,"text":1156,"url":26,"identifiers":1157},"Davis, 1910, Skin transplantation with a review of 550 cases at the Johns Hopkins Hospital, Johns Hopkins Med J, 15, 307",{},{"id":26,"text":1159,"url":26,"identifiers":1160},"Sabella, 1913, Use of fetal membranes in skin grafting, Med Rec, NY, 83, 478",{},{"id":26,"text":1162,"url":26,"identifiers":1163},"Stern, 1913, The grafting of preserved amniotic membrane to burned and ulcerated skin surfaces substituting skin grafts, JAMA, 60, 973, 10.1001\u002Fjama.1913.04340130021008",{"doi":1164},"10.1001\u002Fjama.1913.04340130021008",{"id":26,"text":1166,"url":26,"identifiers":1167},"Toda, 2007, The potential of amniotic membrane\u002Famnion-derived cells for regeneration of various tissues, J Pharmacol Sci, 105, 215, 10.1254\u002Fjphs.CR0070034",{"doi":1168},"10.1254\u002Fjphs.CR0070034",{"id":26,"text":1170,"url":26,"identifiers":1171},"Miki, 2006, Amnion-derived pluripotent\u002Fmultipotent stem cells, Stem Cell Rev, 2, 133, 10.1007\u002Fs12015-006-0020-0",{"doi":1172},"10.1007\u002Fs12015-006-0020-0",{"id":26,"text":1174,"url":26,"identifiers":1175},"Miki, 2007, Identification of stem cell marker-positive cells by immunofluorescence in term human amnion, J Reprod Immunol, 75, 91, 10.1016\u002Fj.jri.2007.03.017",{"doi":1176},"10.1016\u002Fj.jri.2007.03.017",{"id":26,"text":1178,"url":26,"identifiers":1179},"Miki, 2007, Isolation of amniotic epithelial stem cells, Curr Protoc Stem Cell Biol, 10.1002\u002F9780470151808.sc01e03s3",{"doi":1180},"10.1002\u002F9780470151808.sc01e03s3",{"id":26,"text":1182,"url":26,"identifiers":1183},"Koizumi, 2000, Growth factor mRNA and protein in preserved human amniotic membrane, Curr Eye Res, 20, 173, 10.1076\u002F0271-3683(200003)2031-9FT173",{"doi":1184},"10.1076\u002F0271-3683(200003)2031-9FT173",{"id":26,"text":1186,"url":26,"identifiers":1187},"Mermet, 2007, Use of amniotic membrane transplantation in the treatment of venous leg ulcers, Wound Repair Regen, 15, 459, 10.1111\u002Fj.1524-475X.2007.00252.x",{"doi":1188},"10.1111\u002Fj.1524-475X.2007.00252.x",{"id":26,"text":1190,"url":26,"identifiers":1191},"Yoo, 2011, Characterization of novel human mesenchymal stem cell-containing skin substitutes for the treatment of wounds, Ostomy Wound Manage, 57, 71",{},{"id":26,"text":1193,"url":26,"identifiers":1194},"Bieback, 2010, Mesenchymal stromal cells from human perinatal tissues: From biology to cell therapy, World J Stem Cells, 2, 81, 10.4252\u002Fwjsc.v2.i4.81",{"doi":1195},"10.4252\u002Fwjsc.v2.i4.81",{"id":26,"text":1197,"url":26,"identifiers":1198},"Yew, 2011, Enhancement of wound healing by human multipotent stromal cell conditioned medium: The paracrine factors and p38MAPK activation, Cell Transplant, 20, 693, 10.3727\u002F096368910X550198",{"doi":1199},"10.3727\u002F096368910X550198",{"id":26,"text":1201,"url":26,"identifiers":1202},"Wolbank, 2009, Impact of human amniotic membrane preparation on release of angiogenic factors, J Tissue Eng Regen Med, 3, 651, 10.1002\u002Fterm.207",{"doi":1203},"10.1002\u002Fterm.207",{"id":26,"text":777,"url":26,"identifiers":1205},{},{"id":26,"text":1207,"url":26,"identifiers":1208},"Andree, 1994, In vivo transfer and expression of a human epidermal growth factor gene accelerates wound repair, Proc Natl Acad Sci U S A, 91, 12188, 10.1073\u002Fpnas.91.25.12188",{"doi":1209},"10.1073\u002Fpnas.91.25.12188",false,{"id":1212,"createTime":1213,"updateTime":1214,"relativeEntities":1215,"slug":1216,"properties":1217,"entityType":792,"verifyStatus":25,"verifyTime":1236,"verifyNote":793,"syncStatus":28,"languages":1237,"translateLanguages":1238,"viewCount":36,"primaryUrl":1239,"fullTextUrl":26,"authors":1240,"publicationType":877,"publisherRelationship":1433,"citationCount":1466,"citationInfo":1467,"publishDate":1471,"publishYear":1472,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":1473,"isForceReanalyzing":1210},"a284595a-2f89-4f71-8946-9b0a82008ac2","2024-10-01T09:55:50.485+00:00","2024-12-25T09:02:23.139+00:00",[],"Extracellular-Vesicles-Improve-Post-Stroke-Neuroregeneration-and-Prevent-Postischemic-Immunosuppression",{"mag":1218,"keywords":1220,"pmc":1222,"openalex":1224,"abstract":1226,"title":1229,"pm":1232,"doi":1234},{"VOID":1219},"2177788064",{"VI":1221},"EVs, tế bào gốc trung mô, thiếu máu cục bộ, tái sinh thần kinh, bảo vệ thần kinh, miễn dịch học, đột quỵ, exosomes, tái cấu trúc não, tổn thương não",{"VOID":1223},"4572905",{"VOID":1225},"W2177788064",{"EN":1227,"VI":1228},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:sec>\n                  \u003Cjats:title \u002F>\n                  \u003Cjats:p>Although the initial concepts of stem cell therapy aimed at replacing lost tissue, more recent evidence has suggested that stem and progenitor cells alike promote postischemic neurological recovery by secreted factors that restore the injured brain's capacity to reshape. Specifically, extracellular vesicles (EVs) derived from stem cells such as exosomes have recently been suggested to mediate restorative stem cell effects. In order to define whether EVs indeed improve postischemic neurological impairment and brain remodeling, we systematically compared the effects of mesenchymal stem cell (MSC)-derived EVs (MSC-EVs) with MSCs that were i.v. delivered to mice on days 1, 3, and 5 (MSC-EVs) or on day 1 (MSCs) after focal cerebral ischemia in C57BL6 mice. For as long as 28 days after stroke, motor coordination deficits, histological brain injury, immune responses in the peripheral blood and brain, and cerebral angiogenesis and neurogenesis were analyzed. Improved neurological impairment and long-term neuroprotection associated with enhanced angioneurogenesis were noticed in stroke mice receiving EVs from two different bone marrow-derived MSC lineages. MSC-EV administration closely resembled responses to MSCs and persisted throughout the observation period. Although cerebral immune cell infiltration was not affected by MSC-EVs, postischemic immunosuppression (i.e., B-cell, natural killer cell, and T-cell lymphopenia) was attenuated in the peripheral blood at 6 days after ischemia, providing an appropriate external milieu for successful brain remodeling. Because MSC-EVs have recently been shown to be apparently safe in humans, the present study provides clinically relevant evidence warranting rapid proof-of-concept studies in stroke patients.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Significance\u003C\u002Fjats:title>\n                  \u003Cjats:p>Transplantation of mesenchymal stem cells (MSCs) offers an interesting adjuvant approach next to thrombolysis for treatment of ischemic stroke. However, MSCs are not integrated into residing neural networks but act indirectly, inducing neuroprotection and promoting neuroregeneration. Although the mechanisms by which MSCs act are still elusive, recent evidence has suggested that extracellular vesicles (EVs) might be responsible for MSC-induced effects under physiological and pathological conditions. The present study has demonstrated that EVs are not inferior to MSCs in a rodent stroke model. EVs induce long-term neuroprotection, promote neuroregeneration and neurological recovery, and modulate peripheral post-stroke immune responses. Also, because EVs are well-tolerated in humans, as previously reported, the administration of EVs under clinical settings might set the path for a novel and innovative therapeutic stroke concept without the putative side effects attached to stem cell transplantation.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\n               \u003Cjats:sec>\n                  \u003Cjats:title \u002F>\n                  \u003Cjats:p>Mặc dù các khái niệm ban đầu về liệu pháp tế bào gốc nhằm thay thế mô bị mất, nhưng bằng chứng gần đây đã gợi ý rằng cả tế bào gốc và tiền thân đều thúc đẩy phục hồi thần kinh sau thiếu máu cục bộ thông qua các yếu tố tiết ra giúp phục hồi khả năng tái cấu trúc của não bị tổn thương. Cụ thể, các túi ngoại tiết (EVs) từ các tế bào gốc như exosomes đã được đề xuất gần đây có vai trò trung gian cho các tác dụng phục hồi của tế bào gốc. Để xác định liệu EVs có thực sự cải thiện suy giảm thần kinh sau thiếu máu cục bộ và tái cấu trúc não hay không, chúng tôi đã so sánh có hệ thống các tác động của các túi ngoại tiết (MSC-EVs) từ tế bào gốc trung mô (MSCs) so với MSCs được truyền i.v. vào chuột trong các ngày 1, 3 và 5 (MSC-EVs) hoặc ngày 1 (MSCs) sau khi xảy ra thiếu máu cục bộ não tiêu điểm ở chuột C57BL6. Trong 28 ngày sau khi đột quỵ, các điểm yếu về phối hợp vận động, tổn thương não trên mô học, phản ứng miễn dịch trong máu ngoại vi và não, cùng những thay đổi về tạo mạch và sinh trưởng tâm thần kinh đã được phân tích. Cải thiện suy giảm thần kinh và bảo vệ thần kinh dài hạn kết hợp với tăng cường tạo mạch thần kinh và thần kinh đã được ghi nhận ở các con chuột bị đột quỵ nhận EVs từ hai dòng MSC nguồn gốc tủy xương khác nhau. Việc sử dụng MSC-EV mô phỏng chính xác các phản ứng của MSCs và kéo dài suốt giai đoạn quan sát. Mặc dù sự xâm nhập của tế bào miễn dịch não không bị ảnh hưởng bởi MSC-EVs, sự suy giảm miễn dịch sau thiếu máu cục bộ (tức là B-cell, tế bào giết tự nhiên và lymphopenia tế bào T) đã giảm bớt trong máu ngoại vi ở 6 ngày sau thiếu máu cục bộ, cung cấp môi trường ngoại vi thích hợp cho tái cấu trúc não thành công. Vì các nghiên cứu gần đây cho thấy MSC-EVs an toàn với con người, nghiên cứu này cung cấp bằng chứng lâm sàng quan trọng cần thiết cho các nghiên cứu chứng minh nhanh chóng trong bệnh nhân đột quỵ.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Ý nghĩa\u003C\u002Fjats:title>\n                  \u003Cjats:p>Cấy ghép các tế bào gốc trung mô (MSCs) cung cấp một phương pháp tiếp cận hỗ trợ quan trọng bên cạnh việc làm tan cục máu đông để điều trị đột quỵ thiếu máu cục bộ. Tuy nhiên, MSCs không tích hợp vào các mạng lưới thần kinh cư trú mà hoạt động gián tiếp, gây bảo vệ thần kinh và thúc đẩy tái sinh thần kinh. Mặc dù cơ chế MSCs hoạt động còn chưa rõ ràng, bằng chứng gần đây đã gợi ý rằng các túi ngoại tiết (EVs) có thể chịu trách nhiệm cho các tác dụng gây ra bởi MSCs dưới điều kiện sinh lý và bệnh lý. Nghiên cứu hiện tại đã chứng minh rằng EVs không thua kém MSCs trong mô hình đột quỵ động vật gặm nhấm. EVs gây bảo vệ thần kinh lâu dài, thúc đẩy tái sinh thần kinh và phục hồi chức năng thần kinh, và điều tiết các phản ứng miễn dịch sau đột quỵ ngoại biên. Ngoài ra, vì EVs dung nạp tốt ở người theo báo cáo trước đó, việc sử dụng EVs trong điều kiện lâm sàng có thể mở đường cho một định nghĩa điều trị đột quỵ mới và sáng tạo mà không có các tác dụng phụ dự kiến liên quan đến cấy ghép tế bào gốc.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>",{"EN":1230,"VI":1231},"Extracellular Vesicles Improve Post-Stroke Neuroregeneration and Prevent Postischemic Immunosuppression","Các túi ngoại tiết cải thiện tái sinh thần kinh sau đột quỵ và ngăn ngừa suy giảm miễn dịch sau thiếu máu cục bộ",{"VOID":1233},"26339036",{"VOID":1235},"10.5966\u002Fsctm.2015-0078","2024-10-01T09:55:50.484+00:00",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F4\u002F10\u002F1131-1143\u002F6387853",[1241,1263,1295,1310,1327,1342,1365,1382,1399,1416],{"id":1242,"sortIndex":162,"researcher":26,"roles":1243,"affiliations":1244,"properties":1256},"a99a7aa7-a62d-4eda-ad3b-27baf44a8614",[],[1245],{"id":1246,"sortIndex":36,"affiliation":1247,"properties":26},"18d867e8-b47c-4a04-8e5d-8a017b714f9d",{"id":1248,"createTime":1249,"updateTime":1250,"relativeEntities":1251,"slug":1252,"properties":1253,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"718b55d7-5b76-4baa-a07d-3e2675c04383","2024-01-10T04:02:51.931+00:00","2024-10-01T09:55:50.507+00:00",[],"Institute-for-Transfusion-Medicine-University-Hospital-Essen-University-of-Duisburg-Essen-Essen-Germany",{"title":1254},{"VI":1255},"Institute for Transfusion Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany",{"openalex":1257,"orcid":1259,"title":1261},{"VOID":1258},"A5047833836",{"VOID":1260},"https:\u002F\u002Forcid.org\u002F0000-0002-2842-4820",{"EN":1262},"Stefan Radtke",{"id":1264,"sortIndex":115,"researcher":26,"roles":1265,"affiliations":1266,"properties":1288},"5016a061-244d-49bd-aed1-c20da172e80f",[],[1267,1277],{"id":1268,"sortIndex":115,"affiliation":1269,"properties":26},"0a2d5884-81ef-4a9e-b740-9f4bb042134a",{"id":1270,"createTime":1271,"updateTime":1271,"relativeEntities":1272,"slug":1273,"properties":1274,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"bb0d6c8e-3d67-4298-b986-8275606203fc","2024-10-01T09:55:50.518+00:00",[],"Department-of-Pediatrics-I-University-Hospital-Essen-University-of-Duisburg-Essen-Essen-Germany",{"title":1275},{"EN":1276},"Department of Pediatrics I, University Hospital Essen, University of Duisburg-Essen, Essen, Germany",{"id":1278,"sortIndex":36,"affiliation":1279,"properties":26},"186a7505-825d-4dbb-9216-120e125a4d1d",{"id":1280,"createTime":1281,"updateTime":1282,"relativeEntities":1283,"slug":1284,"properties":1285,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"021f8cea-93cb-4324-9109-77d128e184dd","2024-04-21T20:49:56.255+00:00","2025-06-11T15:33:06.124+00:00",[],"Department-of-Neurology-University-Hospital-Essen-University-of-Duisburg-Essen-Essen-Germany",{"title":1286},{"EN":1287},"Department of Neurology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany",{"openalex":1289,"orcid":1291,"title":1293},{"VOID":1290},"A5016898105",{"VOID":1292},"https:\u002F\u002Forcid.org\u002F0000-0001-8132-7459",{"EN":1294},"Josephine 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Optimizing the success of cell transplantation therapy for stroke, Neurobiol Dis, 37, 275, 10.1016\u002Fj.nbd.2009.10.003",{"doi":1704},"10.1016\u002Fj.nbd.2009.10.003",{"id":26,"text":1706,"url":26,"identifiers":1707},"Doeppner, 2010, Mesenchymal stem cells in the treatment of ischemic stroke: Progress and possibilities, Stem Cells Cloning, 3, 157",{},{"id":26,"text":1709,"url":26,"identifiers":1710},"Onda, 2008, Therapeutic benefits by human mesenchymal stem cells (hMSCs) and Ang-1 gene-modified hMSCs after cerebral ischemia, J Cereb Blood Flow Metab, 28, 329, 10.1038\u002Fsj.jcbfm.9600527",{"doi":1711},"10.1038\u002Fsj.jcbfm.9600527",{"id":26,"text":1713,"url":26,"identifiers":1714},"Doeppner, 2013, MicroRNA-124 protects against focal cerebral ischemia via mechanisms involving Usp14-dependent REST degradation, Acta Neuropathol, 126, 251, 10.1007\u002Fs00401-013-1142-5",{"doi":1715},"10.1007\u002Fs00401-013-1142-5",{"id":26,"text":1717,"url":26,"identifiers":1718},"Komatsu, 2010, Therapeutic time window of mesenchymal stem cells derived from bone marrow after cerebral ischemia, Brain Res, 1334, 84, 10.1016\u002Fj.brainres.2010.04.006",{"doi":1719},"10.1016\u002Fj.brainres.2010.04.006",{"id":26,"text":1721,"url":26,"identifiers":1722},"Caplan, 2011, The MSC: An injury drugstore, Cell Stem Cell, 9, 11, 10.1016\u002Fj.stem.2011.06.008",{"doi":1723},"10.1016\u002Fj.stem.2011.06.008",{"id":26,"text":1725,"url":26,"identifiers":1726},"Pittenger, 2009, Sleuthing the source of regeneration by MSCs, Cell Stem Cell, 5, 8, 10.1016\u002Fj.stem.2009.06.013",{"doi":1727},"10.1016\u002Fj.stem.2009.06.013",{"id":26,"text":1729,"url":26,"identifiers":1730},"van Koppen, 2012, Human embryonic mesenchymal stem cell-derived conditioned medium rescues kidney function in rats with established chronic kidney disease, PLoS One, 7, e38746, 10.1371\u002Fjournal.pone.0038746",{"doi":1731},"10.1371\u002Fjournal.pone.0038746",{"id":26,"text":1733,"url":26,"identifiers":1734},"Famakin, 2014, The immune response to acute focal cerebral ischemia and associated post-stroke immunodepression: A focused review, Aging Dis, 5, 307",{},{"id":26,"text":1736,"url":26,"identifiers":1737},"Vogelgesang, 2010, Functional status of peripheral blood T-cells in ischemic stroke patients, PLoS One, 5, e8718, 10.1371\u002Fjournal.pone.0008718",{"doi":1738},"10.1371\u002Fjournal.pone.0008718",{"id":26,"text":1740,"url":26,"identifiers":1741},"Sheikh, 2011, Mesenchymal stem cell transplantation modulates neuroinflammation in focal cerebral ischemia: Contribution of fractalkine and IL-5, Neurobiol Dis, 41, 717, 10.1016\u002Fj.nbd.2010.12.009",{"doi":1742},"10.1016\u002Fj.nbd.2010.12.009",{"id":26,"text":1744,"url":26,"identifiers":1745},"Yoo, 2013, Immune following suppression mesenchymal stem cell transplantation in the ischemic brain is mediated by TGF-β, Neurobiol Dis, 58, 249, 10.1016\u002Fj.nbd.2013.06.001",{"doi":1746},"10.1016\u002Fj.nbd.2013.06.001",{"id":26,"text":1748,"url":26,"identifiers":1749},"Li, 2012, Mesenchymal stem cells: A double-edged sword in regulating immune responses, Cell Death Differ, 19, 1505, 10.1038\u002Fcdd.2012.26",{"doi":1750},"10.1038\u002Fcdd.2012.26",{"id":1752,"createTime":1753,"updateTime":1754,"relativeEntities":1755,"slug":1756,"properties":1757,"entityType":792,"verifyStatus":25,"verifyTime":1775,"verifyNote":793,"syncStatus":28,"languages":1776,"translateLanguages":1777,"viewCount":36,"primaryUrl":1778,"fullTextUrl":26,"authors":1779,"publicationType":877,"publisherRelationship":1926,"citationCount":1959,"citationInfo":1960,"publishDate":1965,"publishYear":1966,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":1967,"isForceReanalyzing":1210},"1a2bd9e9-b3a5-424c-b525-2da02d823c98","2024-10-03T05:20:14.425+00:00","2025-02-22T15:11:54.619+00:00",[],"Concise-Review-Multifaceted-Characterization-of-Human-Mesenchymal-Stem-Cells-for-Use-in-Regenerative-Medicine",{"mag":1758,"keywords":1760,"pmc":1761,"openalex":1763,"abstract":1765,"title":1768,"pm":1771,"doi":1773},{"VOID":1759},"2765979567",{"VI":777},{"VOID":1762},"5702523",{"VOID":1764},"W2765979567",{"EN":1766,"VI":1767},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Mesenchymal stem cells (MSC) hold great potential for regenerative medicine because of their ability for self-renewal and differentiation into tissue-specific cells such as osteoblasts, chondrocytes, and adipocytes. MSCs orchestrate tissue development, maintenance and repair, and are useful for musculoskeletal regenerative therapies to treat age-related orthopedic degenerative diseases and other clinical conditions. Importantly, MSCs produce secretory factors that play critical roles in tissue repair that support both engraftment and trophic functions (autocrine and paracrine). The development of uniform protocols for both preparation and characterization of MSCs, including standardized functional assays for evaluation of their biological potential, are critical factors contributing to their clinical utility. Quality control and release criteria for MSCs should include cell surface markers, differentiation potential, and other essential cell parameters. For example, cell surface marker profiles (surfactome), bone-forming capacities in ectopic and orthotopic models, as well as cell size and granularity, telomere length, senescence status, trophic factor secretion (secretome), and immunomodulation, should be thoroughly assessed to predict MSC utility for regenerative medicine. We propose that these and other functionalities of MSCs should be characterized prior to use in clinical applications as part of comprehensive and uniform guidelines and release criteria for their clinical-grade production to achieve predictably favorable treatment outcomes for stem cell therapy.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Tế bào gốc trung mô (MSC) có tiềm năng lớn trong y học tái tạo nhờ khả năng tự làm mới và phân hóa thành các tế bào đặc hiệu cho mô như tế bào tạo xương (osteoblast), tế bào sụn (chondrocyte) và tế bào mỡ (adipocyte). MSC điều phối sự phát triển, duy trì và sửa chữa mô, và hữu ích trong các liệu pháp tái tạo cơ xương để điều trị các bệnh thoái hóa khớp do tuổi tác và các tình trạng lâm sàng khác. Quan trọng hơn, MSC sản xuất các yếu tố tiết ra có vai trò quan trọng trong việc sửa chữa mô hỗ trợ cho cả chức năng ghép (engraftment) và chức năng nuôi dưỡng (trophic) (tự nội tiết và ngoại tiết). Việc phát triển các quy trình đồng nhất cho cả việc chuẩn bị và đặc trưng hóa MSC, bao gồm các thử nghiệm chức năng tiêu chuẩn để đánh giá tiềm năng sinh học của chúng, là những yếu tố quan trọng góp phần vào tính khả thi lâm sàng của chúng. Các tiêu chí kiểm soát chất lượng và phát hành cho MSC cần bao gồm các dấu hiệu bề mặt tế bào, tiềm năng phân hóa và các thông số tế bào thiết yếu khác. Ví dụ, hồ sơ dấu hiệu bề mặt tế bào (surfactome), khả năng hình thành xương trong các mô hình ghép và mô hình chuẩn, cũng như kích thước tế bào và độ phân giải, chiều dài telomere, tình trạng lão hóa, sự tiết ra yếu tố nuôi dưỡng (secretome), và điều chỉnh miễn dịch, cần được đánh giá kỹ lưỡng để dự đoán tính khả thi của MSC cho y học tái tạo. Chúng tôi đề xuất rằng những chức năng này và các chức năng khác của MSC nên được đặc trưng trước khi sử dụng trong các ứng dụng lâm sàng như một phần của các hướng dẫn và tiêu chí phát hành đồng bộ cho sản xuất có tiêu chuẩn lâm sàng nhằm đạt được kết quả điều trị dao động thuận lợi dự đoán cho liệu pháp tế bào gốc.\u003C\u002Fjats:p>",{"EN":1769,"VI":1770},"Concise Review: Multifaceted Characterization of Human Mesenchymal Stem Cells for Use in Regenerative Medicine","Tổng quan ngắn gọn: Đặc trưng đa diện của tế bào gốc trung mô người để sử dụng trong y học tái tạo",{"VOID":1772},"29076267",{"VOID":1774},"10.1002\u002Fsctm.17-0129","2024-10-03T05:20:14.424+00:00",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F6\u002F12\u002F2173\u002F6454762",[1780,1821,1842,1859,1882,1899],{"id":1781,"sortIndex":36,"researcher":26,"roles":1782,"affiliations":1783,"properties":1814},"a22fa950-e042-4416-b6e9-f459229daae7",[],[1784,1794,1804],{"id":1785,"sortIndex":115,"affiliation":1786,"properties":26},"16fd9164-9bd6-4823-84b2-dfacd170c06c",{"id":1787,"createTime":1788,"updateTime":1788,"relativeEntities":1789,"slug":1790,"properties":1791,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"10fce6ef-5b33-45d4-8589-434041045f66","2024-10-03T05:20:14.449+00:00",[],"bDepartment-of-Biomedical-Engineering-National-University-of-Singapore-Singapore",{"title":1792},{"EN":1793},"bDepartment of Biomedical Engineering, National University of Singapore, Singapore",{"id":1795,"sortIndex":36,"affiliation":1796,"properties":26},"e3e98d2d-140b-4d0e-a379-ca9d5c4accb2",{"id":1797,"createTime":1798,"updateTime":1798,"relativeEntities":1799,"slug":1800,"properties":1801,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"e4eb67c1-28df-4796-9966-a3bb6fc62ace","2024-10-03T05:20:14.443+00:00",[],"aGlycotherapeutics-Group-Institute-of-Medical-Biology-Agency-for-Science-Technology-and-Research-A-STAR-Singapore",{"title":1802},{"EN":1803},"aGlycotherapeutics Group, Institute of Medical Biology, Agency for Science, Technology and Research (A*STAR), Singapore",{"id":1805,"sortIndex":114,"affiliation":1806,"properties":26},"4a78462f-cf6a-4c3b-a789-67ee8d1e2687",{"id":1807,"createTime":1808,"updateTime":1808,"relativeEntities":1809,"slug":1810,"properties":1811,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"2fc8b5dc-1f7d-4b24-b43e-d43b32dc8b99","2024-10-03T05:20:14.453+00:00",[],"cDepartment-of-Orthopaedic-Surgery-Mayo-Clinic-Rochester-Minnesota-USA",{"title":1812},{"EN":1813},"cDepartment of Orthopaedic Surgery, Mayo Clinic, Rochester, Minnesota, USA",{"openalex":1815,"orcid":1817,"title":1819},{"VOID":1816},"A5089242774",{"VOID":1818},"https:\u002F\u002Forcid.org\u002F0000-0001-8804-8284",{"EN":1820},"Rebekah M. 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Chemistry and Biotechnology, ZHAW School of Life Sciences and Facility Management, Zurich University of Applied Sciences, Switzerland",{"id":1914,"sortIndex":36,"affiliation":1915,"properties":26},"5cdbca8e-b726-4aed-8c37-8817e2ce6511",{"id":1787,"createTime":1788,"updateTime":1788,"relativeEntities":1916,"slug":1790,"properties":1917,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":1918},{"EN":1793},{"openalex":1920,"orcid":1922,"title":1924},{"VOID":1921},"A5075382707",{"VOID":1923},"https:\u002F\u002Forcid.org\u002F0000-0002-2138-6614",{"EN":1925},"Michael 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10.1089\u002Ften.tea.2009.0100",{"doi":2637},"10.1089\u002Ften.tea.2009.0100",{"id":26,"text":2639,"url":26,"identifiers":2640},"Parsch, 2004, Telomere length and telomerase activity during expansion and differentiation of human mesenchymal stem cells and chondrocytes, J Mol Med (Berl), 82, 49, 10.1007\u002Fs00109-003-0506-z",{"doi":2641},"10.1007\u002Fs00109-003-0506-z",{"id":26,"text":2643,"url":26,"identifiers":2644},"Zimmermann, 2003, Lack of telomerase activity in human mesenchymal stem cells, Leukemia, 17, 1146, 10.1038\u002Fsj.leu.2402962",{"doi":2645},"10.1038\u002Fsj.leu.2402962",{"id":26,"text":2647,"url":26,"identifiers":2648},"Sethe, 2006, Aging of mesenchymal stem cells, Ageing Res Rev, 5, 91, 10.1016\u002Fj.arr.2005.10.001",{"doi":2649},"10.1016\u002Fj.arr.2005.10.001",{"id":26,"text":2651,"url":26,"identifiers":2652},"Samsonraj, 2013, Telomere length analysis of human mesenchymal stem cells by quantitative PCR, Gene, 519, 348, 10.1016\u002Fj.gene.2013.01.039",{"doi":2653},"10.1016\u002Fj.gene.2013.01.039",{"id":26,"text":2655,"url":26,"identifiers":2656},"Hemeda, 2014, Evaluation of human platelet lysate versus fetal bovine serum for culture of mesenchymal stromal cells, Cytotherapy, 16, 170, 10.1016\u002Fj.jcyt.2013.11.004",{"doi":2657},"10.1016\u002Fj.jcyt.2013.11.004",{"id":26,"text":2659,"url":26,"identifiers":2660},"Spees, 2004, Internalized antigens must be removed to prepare hypoimmunogenic mesenchymal stem cells for cell and gene therapy, Mol Ther, 9, 747, 10.1016\u002Fj.ymthe.2004.02.012",{"doi":2661},"10.1016\u002Fj.ymthe.2004.02.012",{"id":26,"text":2663,"url":26,"identifiers":2664},"Bieback, 2013, Platelet lysate as replacement for fetal bovine serum in mesenchymal stromal cell cultures, Transfus Med Hemother, 40, 326, 10.1159\u002F000354061",{"doi":2665},"10.1159\u002F000354061",{"id":26,"text":2667,"url":26,"identifiers":2668},"Bieback, 2009, Human alternatives to fetal bovine serum for the expansion of mesenchymal stromal cells from bone marrow, Stem Cells, 27, 2331, 10.1002\u002Fstem.139",{"doi":2669},"10.1002\u002Fstem.139",{"id":26,"text":2671,"url":26,"identifiers":2672},"Wijesinghe, 2017, Affinity selection of FGF2-binding heparan sulfates for ex vivo expansion of human mesenchymal stem cells, J Cell Physiol, 232, 566, 10.1002\u002Fjcp.25454",{"doi":2673},"10.1002\u002Fjcp.25454",{"id":26,"text":2675,"url":26,"identifiers":2676},"Ling, 2016, Effect of heparin on the biological properties and molecular signature of human mesenchymal stem cells, Gene, 576, 292, 10.1016\u002Fj.gene.2015.10.039",{"doi":2677},"10.1016\u002Fj.gene.2015.10.039",{"id":26,"text":2679,"url":26,"identifiers":2680},"Gibson, 2017, Regeneration of articular cartilage by human esc-derived mesenchymal progenitors treated sequentially with BMP-2 and Wnt5a, Stem Cells Translational Medicine, 6, 40, 10.5966\u002Fsctm.2016-0020",{"doi":2681},"10.5966\u002Fsctm.2016-0020",{"id":26,"text":2683,"url":26,"identifiers":2684},"Eaker, 2013, Concise review: Guidance in developing commercializable autologous\u002Fpatient-specific cell therapy manufacturing, Stem Cells Translational Medicine, 2, 871, 10.5966\u002Fsctm.2013-0050",{"doi":2685},"10.5966\u002Fsctm.2013-0050",{"id":26,"text":2687,"url":26,"identifiers":2688},"Muller-Cohn, 2015, Stem Cells in Regenerative Medicine, 341, 10.1002\u002F9781118846193.ch18",{"doi":2689},"10.1002\u002F9781118846193.ch18",{"id":26,"text":2691,"url":26,"identifiers":2692},"Schnitzler, 2016, Bioprocessing of human mesenchymal stem\u002Fstromal cells for therapeutic use: Current technologies and challenges, Biochem Eng J, 108, 3, 10.1016\u002Fj.bej.2015.08.014",{"doi":2693},"10.1016\u002Fj.bej.2015.08.014",{"id":26,"text":2695,"url":26,"identifiers":2696},"Research, 2017, 150",{},{"id":26,"text":2698,"url":26,"identifiers":2699},"Nery, 2013, Human mesenchymal stem cells: From immunophenotyping by flow cytometry to clinical applications, Cytometry Part A, 83A, 48, 10.1002\u002Fcyto.a.22205",{"doi":2700},"10.1002\u002Fcyto.a.22205",{"id":26,"text":2702,"url":26,"identifiers":2703},"Caplan, 2016, The 3Rs of cell therapy, Stem Cells Translational Medicine",{},{"id":26,"text":2705,"url":26,"identifiers":2706},"Gronthos, 2007, A novel monoclonal antibody (STRO-3) identifies an isoform of tissue nonspecific alkaline phosphatase expressed by multipotent bone marrow stromal stem cells, Stem Cells Dev, 16, 953, 10.1089\u002Fscd.2007.0069",{"doi":2707},"10.1089\u002Fscd.2007.0069",{"id":26,"text":2709,"url":26,"identifiers":2710},"Bubnic, 2008",{},{"id":26,"text":2712,"url":26,"identifiers":2713},"Smith, 2004, Isolation of a highly clonogenic and multipotential subfraction of adult stem cells from bone marrow stroma, Stem Cells, 22, 823, 10.1634\u002Fstemcells.22-5-823",{"doi":2714},"10.1634\u002Fstemcells.22-5-823",{"id":26,"text":2716,"url":26,"identifiers":2717},"Gupta, 2013, A double blind randomized placebo controlled phase I\u002FII study assessing the safety and efficacy of allogeneic bone marrow derived mesenchymal stem cell in critical limb ischemia, J Transl Med, 11, 143, 10.1186\u002F1479-5876-11-143",{"doi":2718},"10.1186\u002F1479-5876-11-143",{"id":26,"text":2720,"url":26,"identifiers":2721},"Gupta, 2017, Administration of adult human bone marrow-derived, cultured, pooled, allogeneic mesenchymal stromal cells in critical limb ischemia due to Buerger's disease: Phase II study report suggests clinical efficacy, Stem Cells Translational Medicine, 6, 689, 10.5966\u002Fsctm.2016-0237",{"doi":2722},"10.5966\u002Fsctm.2016-0237",{"id":2724,"createTime":2725,"updateTime":2726,"relativeEntities":2727,"slug":2728,"properties":2729,"entityType":792,"verifyStatus":25,"verifyTime":2725,"verifyNote":793,"syncStatus":28,"languages":2747,"translateLanguages":2748,"viewCount":36,"primaryUrl":2749,"fullTextUrl":26,"authors":2750,"publicationType":877,"publisherRelationship":2872,"citationCount":2903,"citationInfo":2904,"publishDate":2907,"publishYear":1966,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":2908,"isForceReanalyzing":1210},"e1ade20b-5717-4c50-ad6d-fe012694ae1c","2024-10-14T04:23:49.766+00:00","2025-02-22T15:12:53.974+00:00",[],"Cartilage-Regeneration-in-Osteoarthritic-Patients-by-a-Composite-of-Allogeneic-Umbilical-Cord-Blood-Derived-Mesenchymal-Stem-Cells-and-Hyaluronate-Hydrogel-Results-from-a-Clinical-Trial-for-Safety-and-Proof-of-Concept-with-7-Years-of-Extended-Follow-Up",{"mag":2730,"keywords":2732,"pmc":2733,"openalex":2735,"abstract":2737,"title":2740,"pm":2743,"doi":2745},{"VOID":2731},"2511760972",{"VI":777},{"VOID":2734},"5442809",{"VOID":2736},"W2511760972",{"EN":2738,"VI":2739},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>Few methods are available to regenerate articular cartilage defects in patients with osteoarthritis. We aimed to assess the safety and efficacy of articular cartilage regeneration by a novel medicinal product composed of allogeneic human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs). Patients with Kellgren-Lawrence grade 3 osteoarthritis and International Cartilage Repair Society (ICRS) grade 4 cartilage defects were enrolled in this clinical trial. The stem cell-based medicinal product (a composite of culture-expanded allogeneic hUCB-MSCs and hyaluronic acid hydrogel [Cartistem]) was applied to the lesion site. Safety was assessed by the World Health Organization common toxicity criteria. The primary efficacy outcome was ICRS cartilage repair assessed by arthroscopy at 12 weeks. The secondary efficacy outcome was visual analog scale (VAS) score for pain on walking. During a 7-year extended follow-up, we evaluated safety, VAS score, International Knee Documentation Committee (IKDC) subjective score, magnetic resonance imaging (MRI) findings, and histological evaluations. Seven participants were enrolled. Maturing repair tissue was observed at the 12-week arthroscopic evaluation. The VAS and IKDC scores were improved at 24 weeks. The improved clinical outcomes were stable over 7 years of follow-up. The histological findings at 1 year showed hyaline-like cartilage. MRI at 3 years showed persistence of the regenerated cartilage. Only five mild to moderate treatment-emergent adverse events were observed. There were no cases of osteogenesis or tumorigenesis over 7 years. The application of this novel stem cell-based medicinal product appears to be safe and effective for the regeneration of durable articular cartilage in osteoarthritic knees.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm Tắt\u003C\u002Fjats:title>\n               \u003Cjats:p>Chỉ có một vài phương pháp có sẵn để tái tạo các khuyết tật sụn khớp ở bệnh nhân bị thoái hóa khớp. Chúng tôi nhằm mục tiêu đánh giá độ an toàn và hiệu quả của việc tái tạo sụn khớp thông qua một sản phẩm dược phẩm mới được chế tạo từ tế bào gốc trung mô (hUCB-MSCs) lấy từ máu dây rốn người đồng loại. Các bệnh nhân bị thoái hóa khớp Kellgren-Lawrence độ 3 và có khuyết tật sụn độ 4 theo Tiêu Chí Sửa Chữa Sụn Quốc Tế (ICRS) đã được ghi danh vào thử nghiệm lâm sàng này. Sản phẩm dược phẩm dựa trên tế bào gốc (composite của hUCB-MSCs nhân nuôi và gel hyaluronic acid [Cartistem]) được áp dụng vào vị trí tổn thương. Độ an toàn được đánh giá bằng tiêu chí độc tính chung của Tổ Chức Y Tế Thế Giới. Kết quả chính đánh giá hiệu quả là sửa chữa sụn ICRS được đánh giá bằng nội soi sau 12 tuần. Kết quả thứ cấp là điểm số thang đánh giá đau (VAS) khi đi lại. Trong suốt 7 năm theo dõi mở rộng, chúng tôi đã đánh giá độ an toàn, điểm VAS, điểm chủ quan theo Ủy Ban Tài Liệu Gối Quốc Tế (IKDC), kết quả hình ảnh cộng hưởng từ (MRI), và đánh giá mô học. Bảy người tham gia đã được ghi danh. Mô sụn phục hồi đang phát triển được quan sát thấy trong đánh giá nội soi sau 12 tuần. Điểm VAS và IKDC đã cải thiện sau 24 tuần. Các kết quả lâm sàng được cải thiện ổn định trong suốt 7 năm theo dõi. Các phát hiện mô học sau 1 năm cho thấy có sụn tương tự như sụn hyaline. MRI sau 3 năm cho thấy sự tồn tại của sụn tái tạo. Chỉ có năm trường hợp biến chứng nhẹ đến vừa được ghi nhận. Không có trường hợp tạo xương hay khối u nào được phát hiện trong 7 năm theo dõi. Việc áp dụng sản phẩm dược phẩm mới dựa trên tế bào gốc này dường như là an toàn và hiệu quả cho việc tái tạo sụn khớp bền vững ở khớp gối bị thoái hóa.",{"EN":2741,"VI":2742},"Cartilage Regeneration in Osteoarthritic Patients by a Composite of Allogeneic Umbilical Cord Blood-Derived Mesenchymal Stem Cells and Hyaluronate Hydrogel: Results from a Clinical Trial for Safety and Proof-of-Concept with 7 Years of Extended Follow-Up","Tái Tạo Sụn Khớp Ở Bệnh Nhân Bị Thoái Hóa Khớp Qua Hợp Chất Chứa Tế Bào Gốc Từ Máu Dây Rốn Và Gel Hyaluronate: Kết Quả Từ Một Nghiên Cứu Lâm Sàng Đánh Giá An Toàn Và Chứng Minh Khái Niệm Với Thời Gian Theo Dõi Kéo Dài 7 Năm",{"VOID":2744},"28191757",{"VOID":2746},"10.5966\u002Fsctm.2016-0157",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F6\u002F2\u002F613\u002F6404831",[2751,2792,2813,2834,2851],{"id":2752,"sortIndex":115,"researcher":26,"roles":2753,"affiliations":2754,"properties":2785},"df2cce47-e173-4a16-8299-0bcf30cd18f0",[],[2755,2765,2775],{"id":2756,"sortIndex":115,"affiliation":2757,"properties":26},"36a171f6-f7e5-41f4-a640-54f0dc192b2a",{"id":2758,"createTime":2759,"updateTime":2759,"relativeEntities":2760,"slug":2761,"properties":2762,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"1a0aba5f-da15-4f1b-b0de-9da8acd997a1","2024-10-14T04:23:49.798+00:00",[],"cStem-Cell-Regenerative-Medicine-Research-Institute-Samsung-Medical-Center-Sungkyunkwan-University-School-of-Medicine-Seoul-Republic-of-Korea",{"title":2763},{"EN":2764},"cStem Cell & Regenerative Medicine Research Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea",{"id":2766,"sortIndex":36,"affiliation":2767,"properties":26},"07627f92-2aa9-46b9-9c7e-15153a46c584",{"id":2768,"createTime":2769,"updateTime":2769,"relativeEntities":2770,"slug":2771,"properties":2772,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"5283a4fa-1815-4429-a119-22eebc0de9cf","2024-10-14T04:23:49.793+00:00",[],"bDepartment-of-Orthopedic-Surgery-Samsung-Medical-Center-Sungkyunkwan-University-School-of-Medicine-Seoul-Republic-of-Korea",{"title":2773},{"EN":2774},"bDepartment of Orthopedic Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea",{"id":2776,"sortIndex":114,"affiliation":2777,"properties":26},"f427a438-8e00-43e0-a748-7782b914c3aa",{"id":2778,"createTime":2779,"updateTime":2779,"relativeEntities":2780,"slug":2781,"properties":2782,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"15c038a3-0c9c-4fee-b9c0-082f94c67c34","2024-10-14T04:23:49.803+00:00",[],"dDepartment-of-Health-Sciences-and-Technology-Samsung-Advanced-Institute-of-Health-Sciences-and-Technology-Sungkyunkwan-University-Seoul-Republic-of-Korea",{"title":2783},{"EN":2784},"dDepartment of Health Sciences and Technology, Samsung Advanced Institute of Health Sciences and Technology, Sungkyunkwan University, Seoul, Republic of Korea",{"openalex":2786,"orcid":2788,"title":2790},{"VOID":2787},"A5002118713",{"VOID":2789},"https:\u002F\u002Forcid.org\u002F0000-0001-5123-6513",{"EN":2791},"Chul‐Won Ha",{"id":2793,"sortIndex":111,"researcher":26,"roles":2794,"affiliations":2795,"properties":2806},"6b5468ea-16ed-4a85-a5ed-7d3e9f8655b9",[],[2796],{"id":2797,"sortIndex":36,"affiliation":2798,"properties":26},"d43dfa7c-e33e-437b-bd59-57af8497aee6",{"id":2799,"createTime":2800,"updateTime":2800,"relativeEntities":2801,"slug":2802,"properties":2803,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"727ffbec-a8fa-4159-a6dc-b09c7dfd7cae","2024-10-14T04:23:49.838+00:00",[],"fDepartment-of-Orthopedic-Surgery-Jeju-National-University-Hospital-Jeju-National-University-School-of-Medicine-Jeju-Republic-of-Korea",{"title":2804},{"EN":2805},"fDepartment of Orthopedic Surgery, Jeju National University Hospital, Jeju National University School of Medicine, Jeju, Republic of Korea",{"openalex":2807,"orcid":2809,"title":2811},{"VOID":2808},"A5101902029",{"VOID":2810},"https:\u002F\u002Forcid.org\u002F0000-0002-9156-1203",{"EN":2812},"Yong‐Geun Park",{"id":2814,"sortIndex":59,"researcher":26,"roles":2815,"affiliations":2816,"properties":2827},"bc1cc49a-7a25-47fc-8dcb-52ff507f9bdb",[],[2817],{"id":2818,"sortIndex":36,"affiliation":2819,"properties":26},"1309c5b3-a815-4042-b372-88d37e566841",{"id":2820,"createTime":2821,"updateTime":2821,"relativeEntities":2822,"slug":2823,"properties":2824,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"d0799d8d-044b-4dc1-aaf7-e87d5928b522","2024-10-14T04:23:49.824+00:00",[],"eDepartment-of-Radiology-Samsung-Medical-Center-Sungkyunkwan-University-School-of-Medicine-Seoul-Republic-of-Korea",{"title":2825},{"EN":2826},"eDepartment of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea",{"openalex":2828,"orcid":2830,"title":2832},{"VOID":2829},"A5022690482",{"VOID":2831},"https:\u002F\u002Forcid.org\u002F0000-0002-7822-5344",{"EN":2833},"Young Cheol Yoon",{"id":2835,"sortIndex":114,"researcher":26,"roles":2836,"affiliations":2837,"properties":2844},"cc8e632a-0768-4c9a-ae99-45f4f32ecb6b",[],[2838],{"id":2839,"sortIndex":36,"affiliation":2840,"properties":26},"483cf89a-d97e-4b30-a205-b8481795a0f9",{"id":2768,"createTime":2769,"updateTime":2769,"relativeEntities":2841,"slug":2771,"properties":2842,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":2843},{"EN":2774},{"openalex":2845,"orcid":2847,"title":2849},{"VOID":2846},"A5003220970",{"VOID":2848},"https:\u002F\u002Forcid.org\u002F0000-0002-7808-8554",{"EN":2850},"Choong‐Hee Lee",{"id":2852,"sortIndex":36,"researcher":26,"roles":2853,"affiliations":2854,"properties":2865},"2675971d-6cb2-4de4-8668-e6156e199d71",[],[2855],{"id":2856,"sortIndex":36,"affiliation":2857,"properties":26},"40e816fe-fb35-4e52-9270-df215b822852",{"id":2858,"createTime":2859,"updateTime":2859,"relativeEntities":2860,"slug":2861,"properties":2862,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"d1a1d28b-fc15-49bb-9345-58ece79e76aa","2024-10-14T04:23:49.781+00:00",[],"aDepartment-of-Orthopedic-Surgery-Chung-Ang-University-Hospital-Chung-Ang-University-College-of-Medicine-Seoul-Republic-of-Korea",{"title":2863},{"EN":2864},"aDepartment of Orthopedic Surgery, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Republic of Korea",{"openalex":2866,"orcid":2868,"title":2870},{"VOID":2867},"A5101902027",{"VOID":2869},"https:\u002F\u002Forcid.org\u002F0000-0002-3741-2311",{"EN":2871},"Yong‐Beom Park",{"url":26,"publisher":2873,"properties":2898},{"id":659,"createTime":660,"updateTime":661,"relativeEntities":2874,"slug":663,"properties":2875,"entityType":24,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"subjectFields":2881,"manageAffiliations":2882,"indexDatabases":2883,"url":762,"thumbnailPath":26,"statistic":26,"gsStatistic":26,"type":26,"analyzePriority":26},[],{"country":2876,"issn":2877,"introduce":2878,"eissn":2879,"title":2880},{"VOID":666},{"VOID":668},{"EN":670},{"VOID":672},{"EN":674},[],[],[2884,2891],{"id":742,"indexDatabase":2885,"url":755,"indexYears":756,"academicFieldIds":2890,"indexDatabaseRanking":761},{"id":744,"createTime":745,"updateTime":746,"relativeEntities":2886,"label":2887,"description":2888,"key":752,"publicationTags":2889,"standard":26},[],{"EN":749,"VI":749},{"EN":749,"VI":751},[754],[758,759,760],{"id":723,"indexDatabase":2892,"url":738,"indexYears":26,"academicFieldIds":2897,"indexDatabaseRanking":26},{"id":725,"createTime":726,"updateTime":727,"relativeEntities":2893,"label":2894,"description":2895,"key":734,"publicationTags":2896,"standard":26},[],{"EN":730,"VI":730},{"VI":732,"EN":733},[736,737],[740],{"volume":2899,"pages":2900,"issue":2902},{"VOID":1954},{"VOID":2901},"613-621",{"VOID":910},355,{"total":2903,"publishYear":26,"statisticByYear":2905},{"2017":173,"2018":516,"2019":240,"2020":569,"2021":44,"2022":2906,"2023":204,"2024":398},82,"2017-02-01",[2909,2913,2917,2921,2925,2929,2933,2937,2941,2944,2948,2952,2956,2960,2964,2968,2972,2976,2980,2984,2988,2992,2996,3000,3004,3008,3010,3014,3018,3022,3026,3029],{"id":26,"text":2910,"url":26,"identifiers":2911},"Seo, 2011, Management of focal chondral lesion in the knee joint, Knee Surg Relat Res, 23, 185, 10.5792\u002Fksrr.2011.23.4.185",{"doi":2912},"10.5792\u002Fksrr.2011.23.4.185",{"id":26,"text":2914,"url":26,"identifiers":2915},"Goyal, 2013, Evidence-based status of microfracture technique: A systematic review of level I and II studies, Arthroscopy, 29, 1579, 10.1016\u002Fj.arthro.2013.05.027",{"doi":2916},"10.1016\u002Fj.arthro.2013.05.027",{"id":26,"text":2918,"url":26,"identifiers":2919},"Mithoefer, 2009, Clinical efficacy of the microfracture technique for articular cartilage repair in the knee: An evidence-based systematic analysis, Am J Sports Med, 37, 2053, 10.1177\u002F0363546508328414",{"doi":2920},"10.1177\u002F0363546508328414",{"id":26,"text":2922,"url":26,"identifiers":2923},"Lee, 2013, Results of microfracture in the osteoarthritic knee with focal full-thickness articular cartilage defects and concomitant medial meniscal tears, Knee Surg Relat Res, 25, 71, 10.5792\u002Fksrr.2013.25.2.71",{"doi":2924},"10.5792\u002Fksrr.2013.25.2.71",{"id":26,"text":2926,"url":26,"identifiers":2927},"Martin, 2003, The role of chondrocyte senescence in the pathogenesis of osteoarthritis and in limiting cartilage repair, J Bone Joint Surg Am, 85-A, 106, 10.2106\u002F00004623-200300002-00014",{"doi":2928},"10.2106\u002F00004623-200300002-00014",{"id":26,"text":2930,"url":26,"identifiers":2931},"Tuan, 2003, Adult mesenchymal stem cells and cell-based tissue engineering, Arthritis Res Ther, 5, 32, 10.1186\u002Far614",{"doi":2932},"10.1186\u002Far614",{"id":26,"text":2934,"url":26,"identifiers":2935},"Koh, 2013, Mesenchymal stem cell injections improve symptoms of knee osteoarthritis, Arthroscopy, 29, 748, 10.1016\u002Fj.arthro.2012.11.017",{"doi":2936},"10.1016\u002Fj.arthro.2012.11.017",{"id":26,"text":2938,"url":26,"identifiers":2939},"Ha, 2014, Mesenchymal stem cells versus fat pad-derived cells, Arthroscopy, 30, 419, 10.1016\u002Fj.arthro.2014.01.015",{"doi":2940},"10.1016\u002Fj.arthro.2014.01.015",{"id":26,"text":2942,"url":26,"identifiers":2943},"Varma, 2010, The new avenues in the management of osteo-arthritis of knee––stem cells, J Indian Med Assoc, 108, 583",{},{"id":26,"text":2945,"url":26,"identifiers":2946},"Jo, 2014, Intra-articular injection of mesenchymal stem cells for the treatment of osteoarthritis of the knee: A proof-of-concept clinical trial, Stem Cells, 32, 1254, 10.1002\u002Fstem.1634",{"doi":2947},"10.1002\u002Fstem.1634",{"id":26,"text":2949,"url":26,"identifiers":2950},"Wakitani, 2002, Human autologous culture expanded bone marrow mesenchymal cell transplantation for repair of cartilage defects in osteoarthritic knees, Osteoarthritis Cartilage, 10, 199, 10.1053\u002Fjoca.2001.0504",{"doi":2951},"10.1053\u002Fjoca.2001.0504",{"id":26,"text":2953,"url":26,"identifiers":2954},"Wakitani, 2011, Safety of autologous bone marrow-derived mesenchymal stem cell transplantation for cartilage repair in 41 patients with 45 joints followed for up to 11 years and 5 months, J Tissue Eng Regen Med, 5, 146, 10.1002\u002Fterm.299",{"doi":2955},"10.1002\u002Fterm.299",{"id":26,"text":2957,"url":26,"identifiers":2958},"Flynn, 2007, UC blood-derived mesenchymal stromal cells: An overview, Cytotherapy, 9, 717, 10.1080\u002F14653240701584578",{"doi":2959},"10.1080\u002F14653240701584578",{"id":26,"text":2961,"url":26,"identifiers":2962},"Kern, 2006, Comparative analysis of mesenchymal stem cells from bone marrow, umbilical cord blood, or adipose tissue, Stem Cells, 24, 1294, 10.1634\u002Fstemcells.2005-0342",{"doi":2963},"10.1634\u002Fstemcells.2005-0342",{"id":26,"text":2965,"url":26,"identifiers":2966},"Chung, 2014, Comparison of articular cartilage repair with different hydrogel-human umbilical cord blood-derived mesenchymal stem cell composites in a rat model, Stem Cell Res Ther, 5, 39, 10.1186\u002Fscrt427",{"doi":2967},"10.1186\u002Fscrt427",{"id":26,"text":2969,"url":26,"identifiers":2970},"Yang, 2004, Mesenchymal stem\u002Fprogenitor cells developed in cultures from UC blood, Cytotherapy, 6, 476, 10.1080\u002F14653240410005041",{"doi":2971},"10.1080\u002F14653240410005041",{"id":26,"text":2973,"url":26,"identifiers":2974},"Trotti, 2003, CTCAE v3.0: Development of a comprehensive grading system for the adverse effects of cancer treatment, Semin Radiat Oncol, 13, 176, 10.1016\u002FS1053-4296(03)00031-6",{"doi":2975},"10.1016\u002FS1053-4296(03)00031-6",{"id":26,"text":2977,"url":26,"identifiers":2978},"Smith, 2005, Arthroscopic assessment of cartilage repair: A validation study of 2 scoring systems, Arthroscopy, 21, 1462, 10.1016\u002Fj.arthro.2005.09.007",{"doi":2979},"10.1016\u002Fj.arthro.2005.09.007",{"id":26,"text":2981,"url":26,"identifiers":2982},"Watanabe, 2006, Delayed gadolinium-enhanced MR to determine glycosaminoglycan concentration in reparative cartilage after autologous chondrocyte implantation: Preliminary results, Radiology, 239, 201, 10.1148\u002Fradiol.2383050173",{"doi":2983},"10.1148\u002Fradiol.2383050173",{"id":26,"text":2985,"url":26,"identifiers":2986},"Veronesi, 2013, Clinical use of bone marrow, bone marrow concentrate, and expanded bone marrow mesenchymal stem cells in cartilage disease, Stem Cells Dev, 22, 181, 10.1089\u002Fscd.2012.0373",{"doi":2987},"10.1089\u002Fscd.2012.0373",{"id":26,"text":2989,"url":26,"identifiers":2990},"Zhang, 2011, Isolation and characterization of mesenchymal stem cells from human umbilical cord blood: reevaluation of critical factors for successful isolation and high ability to proliferate and differentiate to chondrocytes as compared to mesenchymal stem cells from bone marrow and adipose tissue, J Cell Biochem, 112, 1206, 10.1002\u002Fjcb.23042",{"doi":2991},"10.1002\u002Fjcb.23042",{"id":26,"text":2993,"url":26,"identifiers":2994},"Roura, 2015, The role and potential of umbilical cord blood in an era of new therapies: A review, Stem Cell Res Ther, 6, 123, 10.1186\u002Fs13287-015-0113-2",{"doi":2995},"10.1186\u002Fs13287-015-0113-2",{"id":26,"text":2997,"url":26,"identifiers":2998},"Park, 2015, Cartilage repair by human umbilical cord blood-derived mesenchymal stem cells with different hydrogels in a rat model, J Orthop Res, 33, 1580, 10.1002\u002Fjor.22950",{"doi":2999},"10.1002\u002Fjor.22950",{"id":26,"text":3001,"url":26,"identifiers":3002},"Ha, 2015, Cartilage repair using composites of human umbilical cord blood-derived mesenchymal stem cells and hyaluronic acid hydrogel in a minipig model, Stem Cells Translational Medicine, 4, 1044, 10.5966\u002Fsctm.2014-0264",{"doi":3003},"10.5966\u002Fsctm.2014-0264",{"id":26,"text":3005,"url":26,"identifiers":3006},"Lee, 2014, Low immunogenicity of allogeneic human umbilical cord blood-derived mesenchymal stem cells in vitro and in vivo, Biochem Biophys Res Commun, 446, 983, 10.1016\u002Fj.bbrc.2014.03.051",{"doi":3007},"10.1016\u002Fj.bbrc.2014.03.051",{"id":26,"text":1053,"url":26,"identifiers":3009},{"doi":1055},{"id":26,"text":3011,"url":26,"identifiers":3012},"Sato, 2012, Direct transplantation of mesenchymal stem cells into the knee joints of Hartley strain guinea pigs with spontaneous osteoarthritis, Arthritis Res Ther, 14, R31, 10.1186\u002Far3735",{"doi":3013},"10.1186\u002Far3735",{"id":26,"text":3015,"url":26,"identifiers":3016},"Jeong, 2013, Thrombospondin-2 secreted by human umbilical cord blood-derived mesenchymal stem cells promotes chondrogenic differentiation, Stem Cells, 31, 2136, 10.1002\u002Fstem.1471",{"doi":3017},"10.1002\u002Fstem.1471",{"id":26,"text":3019,"url":26,"identifiers":3020},"Brown, 2014, Temporal in vivo assessment of fresh osteochondral allograft transplants to the distal aspect of the femur by dGEMRIC (delayed gadolinium-enhanced MRI of cartilage) and zonal T2 mapping MRI, J Bone Joint Surg Am, 96, 564, 10.2106\u002FJBJS.K.01456",{"doi":3021},"10.2106\u002FJBJS.K.01456",{"id":26,"text":3023,"url":26,"identifiers":3024},"Mithoefer, 2005, The microfracture technique for the treatment of articular cartilage lesions in the knee. A prospective cohort study, J Bone Joint Surg Am, 87, 1911, 10.2106\u002FJBJS.D.02846",{"doi":3025},"10.2106\u002FJBJS.D.02846",{"id":26,"text":3027,"url":26,"identifiers":3028},"Williams, 2007, Microfracture: Indications, technique, and results, Instr Course Lect, 56, 419",{},{"id":26,"text":3030,"url":26,"identifiers":3031},"Filardo, 2013, Matrix-assisted autologous chondrocyte transplantation for cartilage regeneration in osteoarthritic knees: Results and failures at midterm follow-up, Am J Sports Med, 41, 95, 10.1177\u002F0363546512463675",{"doi":3032},"10.1177\u002F0363546512463675",{"id":3034,"createTime":3035,"updateTime":3036,"relativeEntities":3037,"slug":3038,"properties":3039,"entityType":792,"verifyStatus":25,"verifyTime":3035,"verifyNote":793,"syncStatus":28,"languages":3057,"translateLanguages":3058,"viewCount":36,"primaryUrl":3059,"fullTextUrl":26,"authors":3060,"publicationType":877,"publisherRelationship":3097,"citationCount":3128,"citationInfo":3129,"publishDate":3131,"publishYear":1966,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":3132,"isForceReanalyzing":1210},"d21a1baf-a8e7-402a-a881-545b6369e563","2024-10-04T11:16:53.309+00:00","2025-02-22T15:13:52.711+00:00",[],"Bone-Marrow-Derived-Mesenchymal-Stem-Cells-Derived-Exosomes-Promote-Survival-of-Retinal-Ganglion-Cells-Through-miRNA-Dependent-Mechanisms",{"mag":3040,"keywords":3042,"pmc":3043,"openalex":3045,"abstract":3047,"title":3050,"pm":3053,"doi":3055},{"VOID":3041},"2581455542",{"VI":777},{"VOID":3044},"5442835",{"VOID":3046},"W2581455542",{"EN":3048,"VI":3049},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>The loss of retinal ganglion cells (RGC) and their axons is one of the leading causes of blindness and includes traumatic (optic neuropathy) and degenerative (glaucoma) eye diseases. Although no clinical therapies are in use, mesenchymal stem cells (MSC) have demonstrated significant neuroprotective and axogenic effects on RGC in both of the aforementioned models. Recent evidence has shown that MSC secrete exosomes, membrane enclosed vesicles (30–100 nm) containing proteins, mRNA and miRNA which can be delivered to nearby cells. The present study aimed to isolate exosomes from bone marrow-derived MSC (BMSC) and test them in a rat optic nerve crush (ONC) model. Treatment of primary retinal cultures with BMSC-exosomes demonstrated significant neuroprotective and neuritogenic effects. Twenty-one days after ONC and weekly intravitreal exosome injections; optical coherence tomography, electroretinography, and immunohistochemistry was performed. BMSC-derived exosomes promoted statistically significant survival of RGC and regeneration of their axons while partially preventing RGC axonal loss and RGC dysfunction. Exosomes successfully delivered their cargo into inner retinal layers and the effects were reliant on miRNA, demonstrated by the diminished therapeutic effects of exosomes derived from BMSC after knockdown of Argonaute-2, a key miRNA effector molecule. This study supports the use of BMSC-derived exosomes as a cell-free therapy for traumatic and degenerative ocular disease.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\n               \u003Cjats:p>Mất tế bào thần kinh hạch võng mạc (RGC) và các sợi trục của chúng là một trong những nguyên nhân hàng đầu gây mù lòa, bao gồm các bệnh về mắt chấn thương (bệnh thần kinh thị giác) và thoái hóa (cườm nước). Mặc dù không có liệu pháp lâm sàng nào được sử dụng, tế bào gốc trung mô (MSC) đã chứng tỏ có tác dụng bảo vệ thần kinh và thúc đẩy sự hình thành sợi thần kinh đáng kể đối với RGC trong cả hai mô hình nêu trên. Bằng chứng gần đây cho thấy MSC tiết ra exosome, các túi màng bao gồm (30–100 nm) chứa protein, mRNA và miRNA có thể được chuyển đến các tế bào lân cận. Nghiên cứu hiện tại nhằm mục đích phân lập exosome từ MSC lấy từ tủy xương (BMSC) và thử nghiệm chúng trong mô hình nghiền dây thần kinh thị giác ở chuột (ONC). Việc điều trị các mô hình văn hóa võng mạc chính bằng exosome BMSC cho thấy tác dụng bảo vệ thần kinh và thúc đẩy hình thành sợi thần kinh đáng kể. Hai mươi mốt ngày sau ONC và tiêm thuốc vào thủy tinh thể hàng tuần; chụp ánh sáng đồng bộ quang học, điện sinh lý võng mạc và hóa miễn dịch đã được thực hiện. Exosome nguồn gốc từ BMSC đã thúc đẩy sự sống sót đáng kể của RGC và sự tái sinh các sợi trục của chúng trong khi một phần ngăn chặn mất mát sợi trục RGC và rối loạn chức năng RGC. Exosome đã thành công trong việc chuyển tải hàng hóa của chúng vào các lớp trong của võng mạc và các hiệu ứng phụ thuộc vào miRNA, được chứng minh bằng việc giảm hiệu ứng điều trị của các exosome lấy từ BMSC sau khi gạt bỏ Argonaute-2, một phân tử tác động miRNA quan trọng. Nghiên cứu này ủng hộ việc sử dụng exosome lấy từ BMSC như một liệu pháp không dựa trên tế bào cho căn bệnh mắt chấn thương và thoái hóa.\u003C\u002Fjats:p>",{"EN":3051,"VI":3052},"Bone Marrow-Derived Mesenchymal Stem Cells-Derived Exosomes Promote Survival of Retinal Ganglion Cells Through miRNA-Dependent Mechanisms","Exosome từ tế bào gốc trung mô lấy từ tủy xương thúc đẩy sự sống sót của tế bào thần kinh hạch võng mạc thông qua cơ chế phụ thuộc vào miRNA",{"VOID":3054},"28198592",{"VOID":3056},"10.1002\u002Fsctm.16-0428",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F6\u002F4\u002F1273\u002F6404678",[3061,3082],{"id":3062,"sortIndex":36,"researcher":26,"roles":3063,"affiliations":3064,"properties":3075},"2add27ce-3648-4b4d-ac20-82e4ac9407ee",[],[3065],{"id":3066,"sortIndex":36,"affiliation":3067,"properties":26},"e0f4ad01-3bdf-4b8a-ab3a-cd93328a641f",{"id":3068,"createTime":3069,"updateTime":3069,"relativeEntities":3070,"slug":3071,"properties":3072,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"2fc4607b-4f5e-4255-aa5e-75b1628fd27f","2024-10-04T11:16:53.329+00:00",[],"Section-of-Retinal-Ganglion-Cell-Biology-Laboratory-of-Retinal-Cell-and-Molecular-Biology-National-Eye-Institute-National-Institutes-of-Health-Bethesda-Maryland-USA",{"title":3073},{"EN":3074},"Section of Retinal Ganglion Cell Biology, Laboratory of Retinal Cell and Molecular Biology, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA",{"openalex":3076,"orcid":3078,"title":3080},{"VOID":3077},"A5036095079",{"VOID":3079},"https:\u002F\u002Forcid.org\u002F0000-0001-5855-0097",{"EN":3081},"Ben Mead",{"id":3083,"sortIndex":115,"researcher":26,"roles":3084,"affiliations":3085,"properties":3092},"2929c47e-5591-4ec3-bf72-1228ebdce242",[],[3086],{"id":3087,"sortIndex":36,"affiliation":3088,"properties":26},"ff90e132-41c6-48a8-b905-4e412259132a",{"id":3068,"createTime":3069,"updateTime":3069,"relativeEntities":3089,"slug":3071,"properties":3090,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":3091},{"EN":3074},{"openalex":3093,"title":3095},{"VOID":3094},"A5079651670",{"EN":3096},"Stanislav I. Tomarev",{"url":26,"publisher":3098,"properties":3123},{"id":659,"createTime":660,"updateTime":661,"relativeEntities":3099,"slug":663,"properties":3100,"entityType":24,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"subjectFields":3106,"manageAffiliations":3107,"indexDatabases":3108,"url":762,"thumbnailPath":26,"statistic":26,"gsStatistic":26,"type":26,"analyzePriority":26},[],{"country":3101,"issn":3102,"introduce":3103,"eissn":3104,"title":3105},{"VOID":666},{"VOID":668},{"EN":670},{"VOID":672},{"EN":674},[],[],[3109,3116],{"id":742,"indexDatabase":3110,"url":755,"indexYears":756,"academicFieldIds":3115,"indexDatabaseRanking":761},{"id":744,"createTime":745,"updateTime":746,"relativeEntities":3111,"label":3112,"description":3113,"key":752,"publicationTags":3114,"standard":26},[],{"EN":749,"VI":749},{"EN":749,"VI":751},[754],[758,759,760],{"id":723,"indexDatabase":3117,"url":738,"indexYears":26,"academicFieldIds":3122,"indexDatabaseRanking":26},{"id":725,"createTime":726,"updateTime":727,"relativeEntities":3118,"label":3119,"description":3120,"key":734,"publicationTags":3121,"standard":26},[],{"EN":730,"VI":730},{"VI":732,"EN":733},[736,737],[740],{"volume":3124,"pages":3125,"issue":3127},{"VOID":1954},{"VOID":3126},"1273-1285",{"VOID":1461},338,{"total":3128,"publishYear":26,"statisticByYear":3130},{"2017":52,"2018":239,"2019":257,"2020":517,"2021":44,"2022":254,"2023":282,"2024":402},"2017-04-01",[3133,3135,3139,3143,3147,3150,3154,3158,3162,3166,3170,3173,3177,3181,3185,3189,3193,3197,3201,3205,3209,3212,3216,3218,3222,3226,3230,3234,3237,3239,3243,3247,3251,3253,3257,3261,3265,3269,3273,3277,3281,3285,3289,3293,3297,3301,3305,3309,3313,3317,3321,3325,3329,3333,3337,3341,3345,3347,3351,3355,3359,3363,3367],{"id":26,"text":1995,"url":26,"identifiers":3134},{},{"id":26,"text":3136,"url":26,"identifiers":3137},"Zuk, 2001, Multilineage cells from human adipose tissue: Implications for cell-based therapies, Tissue Eng, 7, 211, 10.1089\u002F107632701300062859",{"doi":3138},"10.1089\u002F107632701300062859",{"id":26,"text":3140,"url":26,"identifiers":3141},"Gronthos, 2000, Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo, Proc Natl Acad Sci USA, 97, 13625, 10.1073\u002Fpnas.240309797",{"doi":3142},"10.1073\u002Fpnas.240309797",{"id":26,"text":3144,"url":26,"identifiers":3145},"Kogler, 2004, A new human somatic stem cell from placental cord blood with intrinsic pluripotent differentiation potential, J Exp Med, 200, 123, 10.1084\u002Fjem.20040440",{"doi":3146},"10.1084\u002Fjem.20040440",{"id":26,"text":3148,"url":26,"identifiers":3149},"Berry, 2008, Regeneration of axons in the visual system, Restor Neurol Neurosci, 26, 147",{},{"id":26,"text":3151,"url":26,"identifiers":3152},"Mead, 2015, Stem cell treatment of degenerative eye disease, Stem Cell Res, 14, 243, 10.1016\u002Fj.scr.2015.02.003",{"doi":3153},"10.1016\u002Fj.scr.2015.02.003",{"id":26,"text":3155,"url":26,"identifiers":3156},"Mead, 2014, Paracrine-mediated neuroprotection and neuritogenesis of axotomised retinal ganglion cells by human dental pulp stem cells: comparison with human bone marrow and adipose-derived mesenchymal stem cells, PLoS One, 9, e109305, 10.1371\u002Fjournal.pone.0109305",{"doi":3157},"10.1371\u002Fjournal.pone.0109305",{"id":26,"text":3159,"url":26,"identifiers":3160},"Mead, 2014, Dental pulp stem cells, a paracrine-mediated therapy for the retina, Neural Regen Res, 9, 577, 10.4103\u002F1673-5374.130089",{"doi":3161},"10.4103\u002F1673-5374.130089",{"id":26,"text":3163,"url":26,"identifiers":3164},"Levkovitch-Verbin, 2010, Intravitreal injections of neurotrophic factors secreting mesenchymal stem cells are neuroprotective in rat eyes following optic nerve transection, Invest Ophthalmol Vis Sci, 51, 6394, 10.1167\u002Fiovs.09-4310",{"doi":3165},"10.1167\u002Fiovs.09-4310",{"id":26,"text":3167,"url":26,"identifiers":3168},"Mead, 2013, Intravitreally transplanted dental pulp stem cells promote neuroprotection and axon regeneration of retinal ganglion cells after optic nerve injury, Invest Ophthalmol Vis Sci, 54, 7544, 10.1167\u002Fiovs.13-13045",{"doi":3169},"10.1167\u002Fiovs.13-13045",{"id":26,"text":3171,"url":26,"identifiers":3172},"Tan, 2015, The therapeutic effects of bone marrow mesenchymal stem cells after optic nerve damage in the adult rat, Clin Interv Aging, 10, 487",{},{"id":26,"text":3174,"url":26,"identifiers":3175},"Zwart, 2009, Umbilical cord blood mesenchymal stromal cells are neuroprotective and promote regeneration in a rat optic tract model, Exp Neurol, 216, 439, 10.1016\u002Fj.expneurol.2008.12.028",{"doi":3176},"10.1016\u002Fj.expneurol.2008.12.028",{"id":26,"text":3178,"url":26,"identifiers":3179},"Mead, 2016, Mesenchymal stromal cell-mediated neuroprotection and 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10.1371\u002Fjournal.pone.0110722",{"doi":3320},"10.1371\u002Fjournal.pone.0110722",{"id":26,"text":3322,"url":26,"identifiers":3323},"Mead, 2016, Evaluating retinal ganglion cell loss and dysfunction, Exp Eye Res, 151, 96, 10.1016\u002Fj.exer.2016.08.006",{"doi":3324},"10.1016\u002Fj.exer.2016.08.006",{"id":26,"text":3326,"url":26,"identifiers":3327},"Duan, 2015, Subtype-specific regeneration of retinal ganglion cells following axotomy: Effects of osteopontin and mTOR signaling, Neuron, 85, 1244, 10.1016\u002Fj.neuron.2015.02.017",{"doi":3328},"10.1016\u002Fj.neuron.2015.02.017",{"id":26,"text":3330,"url":26,"identifiers":3331},"Ha, 2014, Regulation of microRNA biogenesis, Nat Rev Mol Cell Biol, 15, 509, 10.1038\u002Fnrm3838",{"doi":3332},"10.1038\u002Fnrm3838",{"id":26,"text":3334,"url":26,"identifiers":3335},"Guduric-Fuchs, 2012, Selective extracellular vesicle-mediated export of an overlapping set of microRNAs from multiple cell types, BMC Genomics, 13, 357, 10.1186\u002F1471-2164-13-357",{"doi":3336},"10.1186\u002F1471-2164-13-357",{"id":26,"text":3338,"url":26,"identifiers":3339},"Baglio, 2015, Human bone marrow- and adipose-mesenchymal stem cells secrete exosomes enriched in distinctive miRNA and tRNA species, Stem Cell Res Ther, 6, 127, 10.1186\u002Fs13287-015-0116-z",{"doi":3340},"10.1186\u002Fs13287-015-0116-z",{"id":26,"text":3342,"url":26,"identifiers":3343},"Qian, 2016, Exosomal microRNAs derived from umbilical mesenchymal stem cells inhibit Hepatitis C virus infection, Stem Cells Transl Med, 10.5966\u002Fsctm.2015-0348",{"doi":3344},"10.5966\u002Fsctm.2015-0348",{"id":26,"text":2455,"url":26,"identifiers":3346},{"doi":2457},{"id":26,"text":3348,"url":26,"identifiers":3349},"Park, 2008, Promoting axon regeneration in the adult CNS by modulation of the PTEN\u002FmTOR pathway, Science, 322, 963, 10.1126\u002Fscience.1161566",{"doi":3350},"10.1126\u002Fscience.1161566",{"id":26,"text":3352,"url":26,"identifiers":3353},"Berry, 2016, Prospects for mTOR-mediated functional repair after central nervous system trauma, Neurobiol Dis, 85, 99, 10.1016\u002Fj.nbd.2015.10.002",{"doi":3354},"10.1016\u002Fj.nbd.2015.10.002",{"id":26,"text":3356,"url":26,"identifiers":3357},"Meng, 2007, MicroRNA-21 regulates expression of the PTEN tumor suppressor gene in human hepatocellular cancer, Gastroenterology, 133, 647, 10.1053\u002Fj.gastro.2007.05.022",{"doi":3358},"10.1053\u002Fj.gastro.2007.05.022",{"id":26,"text":3360,"url":26,"identifiers":3361},"Katakowski, 2013, Exosomes from marrow stromal cells expressing miR-146b inhibit glioma growth, Cancer Lett, 335, 201, 10.1016\u002Fj.canlet.2013.02.019",{"doi":3362},"10.1016\u002Fj.canlet.2013.02.019",{"id":26,"text":3364,"url":26,"identifiers":3365},"Koprivica, 2005, EGFR activation mediates inhibition of axon regeneration by myelin and chondroitin sulfate proteoglycans, Science, 310, 106, 10.1126\u002Fscience.1115462",{"doi":3366},"10.1126\u002Fscience.1115462",{"id":26,"text":3368,"url":26,"identifiers":3369},"Gu, 2016, Exosomes derived from human mesenchymal stem cells promote gastric cancer cell growth and migration via the activation of the Akt pathway, Mol Med Rep, 10.3892\u002Fmmr.2016.5625",{"doi":3370},"10.3892\u002Fmmr.2016.5625",{"id":3372,"createTime":3373,"updateTime":3374,"relativeEntities":3375,"slug":3376,"properties":3377,"entityType":792,"verifyStatus":25,"verifyTime":3373,"verifyNote":793,"syncStatus":28,"languages":3395,"translateLanguages":3396,"viewCount":36,"primaryUrl":3397,"fullTextUrl":26,"authors":3398,"publicationType":877,"publisherRelationship":3664,"citationCount":394,"citationInfo":3695,"publishDate":3697,"publishYear":916,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":3698,"isForceReanalyzing":1210},"b9d53bfc-6c6a-4aca-92f5-a4d7bc02031a","2024-09-30T23:42:58.150+00:00","2025-02-22T15:14:49.669+00:00",[],"Human-Mesenchymal-Stem-Cell-Transfusion-Is-Safe-and-Improves-Liver-Function-in-Acute-on-Chronic-Liver-Failure-Patients",{"mag":3378,"keywords":3380,"pmc":3381,"openalex":3383,"abstract":3385,"title":3388,"pm":3391,"doi":3393},{"VOID":3379},"2143119387",{"VI":777},{"VOID":3382},"3659658",{"VOID":3384},"W2143119387",{"EN":3386,"VI":3387},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>Acute-on-chronic liver failure (ACLF) is a severe, life-threatening complication, and new and efficient therapeutic strategies for liver failure are urgently needed. Mesenchymal stem cell (MSC) transfusions have been shown to reverse fulminant hepatic failure in mice and to improve liver function in patients with end-stage liver diseases. We assessed the safety and initial efficacy of umbilical cord-derived MSC (UC-MSC) transfusions for ACLF patients associated with hepatitis B virus (HBV) infection. A total of 43 ACLF patients were enrolled for this open-labeled and controlled study; 24 patients were treated with UC-MSCs, and 19 patients were treated with saline as controls. UC-MSC therapy was given three times at 4-week intervals. The liver function, adverse events, and survival rates were evaluated during the 48-week or 72-week follow-up period. No significant side effects were observed during the trial. The UC-MSC transfusions significantly increased the survival rates in ACLF patients; reduced the model for end-stage liver disease scores; increased serum albumin, cholinesterase, and prothrombin activity; and increased platelet counts. Serum total bilirubin and alanine aminotransferase levels were significantly decreased after the UC-MSC transfusions. UC-MSC transfusions are safe in the clinic and may serve as a novel therapeutic approach for HBV-associated ACLF patients.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\n               \u003Cjats:p>Suy gan cấp trên nền mãn tính (ACLF) là một biến chứng nghiêm trọng, đe dọa tính mạng, và cần thiết phải có các chiến lược điều trị mới và hiệu quả cho suy gan. Việc truyền tế bào gốc trung mô (MSC) đã được chứng minh là có khả năng đảo ngược tình trạng suy gan cấp tính ở chuột và cải thiện chức năng gan ở bệnh nhân có bệnh gan giai đoạn cuối. Chúng tôi đã đánh giá độ an toàn và hiệu quả ban đầu của việc truyền MSC lấy từ dây rốn (UC-MSC) cho bệnh nhân ACLF liên quan đến nhiễm vi rút viêm gan B (HBV). Tổng cộng 43 bệnh nhân ACLF đã được tham gia vào nghiên cứu này, một nghiên cứu mở và có kiểm soát; 24 bệnh nhân được điều trị bằng UC-MSCs, và 19 bệnh nhân còn lại được điều trị bằng dung dịch muối sinh lý như nhóm chứng. Việc điều trị bằng UC-MSC được thực hiện ba lần tại các khoảng cách 4 tuần. Chức năng gan, các sự kiện bất lợi, và tỷ lệ sống sót đã được đánh giá trong thời gian theo dõi 48 tuần hoặc 72 tuần. Không có tác dụng phụ đáng kể nào được quan sát trong quá trình thử nghiệm. Việc truyền UC-MSC đã làm tăng đáng kể tỷ lệ sống sót ở bệnh nhân ACLF; giảm điểm số mô hình cho bệnh gan giai đoạn cuối; tăng nồng độ albumin huyết thanh, cholinesterase, và hoạt tính prothrombin; và tăng số lượng tiểu cầu. Mức bilirubin toàn phần và alanine aminotransferase trong huyết thanh đã giảm đáng kể sau khi truyền UC-MSC. Việc truyền UC-MSC là an toàn trong lâm sàng và có thể là một phương pháp điều trị mới cho bệnh nhân ACLF liên quan đến HBV.\u003C\u002Fjats:p>",{"EN":3389,"VI":3390},"Human Mesenchymal Stem Cell Transfusion Is Safe and Improves Liver Function in Acute-on-Chronic Liver Failure Patients","Truyền tế bào gốc trung mô người an toàn và cải thiện chức năng gan ở bệnh nhân suy gan cấp trên nền mãn tính",{"VOID":3392},"23197664",{"VOID":3394},"10.5966\u002Fsctm.2012-0034",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F1\u002F10\u002F725-731\u002F6385503",[3399,3421,3438,3455,3470,3487,3504,3521,3538,3566,3581,3598,3615,3632,3649],{"id":3400,"sortIndex":111,"researcher":26,"roles":3401,"affiliations":3402,"properties":3414},"931ed19e-c5a7-426d-9bde-95de6f2d54ba",[],[3403],{"id":3404,"sortIndex":36,"affiliation":3405,"properties":26},"4f25ebd7-b5a3-4f47-a637-6aade526eb84",{"id":3406,"createTime":3407,"updateTime":3408,"relativeEntities":3409,"slug":3410,"properties":3411,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"63e1b68b-4fff-4bc9-92b4-a29853b8c6da","2024-01-16T17:37:18.384+00:00","2024-09-30T23:42:58.172+00:00",[],"Research-Center-for-Biological-Therapy-Institute-of-Translational-Hepatology-Beijing-302-Hospital-Beijing-China",{"title":3412},{"VI":3413},"Research Center for Biological Therapy, Institute of Translational Hepatology,  Beijing 302 Hospital, Beijing, China",{"openalex":3415,"orcid":3417,"title":3419},{"VOID":3416},"A5042360471",{"VOID":3418},"https:\u002F\u002Forcid.org\u002F0009-0001-8318-6888",{"EN":3420},"Junliang Fu",{"id":3422,"sortIndex":103,"researcher":26,"roles":3423,"affiliations":3424,"properties":3431},"ca05eb99-23e1-430b-8980-107f2984b6d3",[],[3425],{"id":3426,"sortIndex":36,"affiliation":3427,"properties":26},"bb104d5b-180b-4bd9-9704-028871b33ca1",{"id":3406,"createTime":3407,"updateTime":3408,"relativeEntities":3428,"slug":3410,"properties":3429,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":3430},{"VI":3413},{"openalex":3432,"orcid":3434,"title":3436},{"VOID":3433},"A5100740368",{"VOID":3435},"https:\u002F\u002Forcid.org\u002F0000-0001-5630-2081",{"EN":3437},"Lei 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10.1111\u002Fj.1440-1746.2011.07024.x",{"doi":3761},"10.1111\u002Fj.1440-1746.2011.07024.x",{"id":26,"text":3763,"url":26,"identifiers":3764},"Peng, 2011, Autologous bone mesenchymal stem cell transplantation in liver failure patients caused by hepatitis B: Short-term and long-term outcomes, Hepatology, 54, 820, 10.1002\u002Fhep.24434",{"doi":3765},"10.1002\u002Fhep.24434",{"id":26,"text":3767,"url":26,"identifiers":3768},"Lu, 2006, Isolation and characterization of human umbilical cord mesenchymal stem cells with hematopoiesis-supportive function and other potentials, Haematologica, 91, 1017",{},{"id":26,"text":3770,"url":26,"identifiers":3771},"Garg, 2012, Granulocyte-colony stimulating factor mobilizes CD34+ cells and improves survival of patients with acute-on-chronic liver failure, Gastroenterology, 142, 505, 10.1053\u002Fj.gastro.2011.11.027",{"doi":3772},"10.1053\u002Fj.gastro.2011.11.027",{"id":26,"text":3774,"url":26,"identifiers":3775},"Zhong, 2010, deficient proliferation of 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Adjuvants for human cell transplantation, Biol Blood Marrow Transplant, 13, 1477, 10.1016\u002Fj.bbmt.2007.08.048",{"doi":3804},"10.1016\u002Fj.bbmt.2007.08.048",{"id":26,"text":3806,"url":26,"identifiers":3807},"Schinköthe, 2008, In vitro secreting profile of human mesenchymal stem cells, Stem Cells Dev, 17, 199, 10.1089\u002Fscd.2007.0175",{"doi":3808},"10.1089\u002Fscd.2007.0175",{"id":26,"text":3810,"url":26,"identifiers":3811},"Fong, 2012, Human umbilical cord Wharton's jelly stem cells and its conditioned medium support hematopoietic stem cell expansion ex vivo, J Cell Biochem, 113, 658, 10.1002\u002Fjcb.23395",{"doi":3812},"10.1002\u002Fjcb.23395",{"id":3814,"createTime":3815,"updateTime":3816,"relativeEntities":3817,"slug":3818,"properties":3819,"entityType":792,"verifyStatus":25,"verifyTime":3815,"verifyNote":793,"syncStatus":28,"languages":3837,"translateLanguages":3838,"viewCount":36,"primaryUrl":3839,"fullTextUrl":26,"authors":3840,"publicationType":877,"publisherRelationship":3879,"citationCount":3911,"citationInfo":3912,"publishDate":3914,"publishYear":916,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":3915,"isForceReanalyzing":1210},"a1553cd1-bcf9-4633-a553-024b448cb3d1","2024-11-27T14:14:08.497+00:00","2025-02-22T15:15:47.407+00:00",[],"Effects-of-Medium-Supplements-on-Proliferation-Differentiation-Potential-and-In-Vitro-Expansion-of-Mesenchymal-Stem-Cells",{"mag":3820,"keywords":3822,"pmc":3823,"openalex":3825,"abstract":3827,"title":3830,"pm":3833,"doi":3835},{"VOID":3821},"2063048290",{"VI":777},{"VOID":3824},"3659663",{"VOID":3826},"W2063048290",{"EN":3828,"VI":3829},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>Mesenchymal stem cells (MSCs) possess great potential for use in regenerative medicine. However, their clinical application may be limited by the ability to expand their cell numbers in vitro while maintaining their differential potentials and stem cell properties. Thus the aim of this study was to test the effect of a range of medium supplements on MSC self-renewal and differentiation potential. Cells were cultured until confluent and subcultured continuously until reaching senescence. Medium supplementation with fibroblast growth factor (FGF)-2, platelet-derived growth factor (PDGF)-BB, ascorbic acid (AA), and epidermal growth factor (EGF) both increased proliferation rate and markedly increased number of cell doublings before reaching senescence, with a greater than 1,000-fold increase in total cell numbers for AA, FGF-2, and PDGF-BB compared with control cultures. Long-term culture was associated with loss of osteogenic\u002Fadipocytic differentiation potential, particularly with FGF-2 supplementation but also with AA, EGF, and PDGF-BB. In addition FGF-2 resulted in reduction in expression of CD146 and alkaline phosphatase, but this was partially reversible on removal of the supplement. Cells expressed surface markers including CD146, CD105, CD44, CD90, and CD71 by flow cytometry throughout, and expression of these putative stem cell markers persisted even after loss of differentiation potentials. Overall, medium supplementation with FGF-2, AA, EGF, and PDGF-BB greatly enhanced the total in vitro expansion capacity of MSC cultures, although differentiation potentials were lost prior to reaching senescence. Loss of differentiation potential was not reflected by changes in stem cell surface marker expression.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\n               \u003Cjats:p>Các tế bào gốc trung mô (MSCs) có tiềm năng lớn trong ứng dụng y học tái tạo. Tuy nhiên, việc ứng dụng lâm sàng của chúng có thể bị hạn chế bởi khả năng mở rộng số lượng tế bào in vitro trong khi vẫn duy trì được tiềm năng phân hóa và các đặc tính của tế bào gốc. Do đó, mục tiêu của nghiên cứu này là kiểm tra ảnh hưởng của một loạt các chất bổ sung trong môi trường nuôi cấy đến khả năng tự tái tạo và phân hóa của MSC. Các tế bào được nuôi cấy cho đến khi đạt đến mật độ tối đa và được tiếp tục cấy chuyền cho đến khi đạt đến giai đoạn lão hóa. Việc bổ sung môi trường với yếu tố tăng trưởng nguyên bào sợi (FGF)-2, yếu tố tăng trưởng nguồn gốc tiểu cầu (PDGF)-BB, axit ascorbic (AA), và yếu tố tăng trưởng biểu bì (EGF) không chỉ làm tăng tốc độ tăng sinh mà còn tăng đáng kể số lần phân chia tế bào trước khi đạt đến giai đoạn lão hóa, với sự gia tăng tổng số tế bào hơn 1.000 lần đối với AA, FGF-2, và PDGF-BB so với các văn hóa đối chứng. Nuôi cấy dài hạn liên quan đến việc mất tiềm năng phân hóa thành tế bào xương\u002Ftế bào mỡ, đặc biệt là với sự bổ sung FGF-2 nhưng cũng với AA, EGF và PDGF-BB. Ngoài ra, FGF-2 đã làm giảm biểu hiện của CD146 và phosphatase kiềm, nhưng điều này có thể phục hồi một phần khi loại bỏ chất bổ sung. Các tế bào biểu hiện các dấu hiệu bề mặt bao gồm CD146, CD105, CD44, CD90 và CD71 được xác định bằng phương pháp phân tích dòng xuyên suốt, và sự biểu hiện của các dấu hiệu tế bào gốc này vẫn tồn tại ngay cả sau khi mất tiềm năng phân hóa. Tổng thể, việc bổ sung môi trường với FGF-2, AA, EGF và PDGF-BB đã tăng cường đáng kể khả năng mở rộng tổng thể in vitro của các văn hóa MSC, mặc dù tiềm năng phân hóa bị mất trước khi đạt đến lão hóa. Mất tiềm năng phân hóa không được phản ánh bằng sự thay đổi trong biểu hiện các dấu hiệu bề mặt tế bào gốc.",{"EN":3831,"VI":3832},"Effects of Medium Supplements on Proliferation, Differentiation Potential, and In Vitro Expansion of Mesenchymal Stem Cells","Ảnh hưởng của các chế phẩm đệm tới sự tăng sinh, khả năng phân biệt và sự mở rộng in vitro của các tế bào gốc trung mô",{"VOID":3834},"23197689",{"VOID":3836},"10.5966\u002Fsctm.2010-0031",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F1\u002F11\u002F771-782\u002F6385489",[3841,3862],{"id":3842,"sortIndex":115,"researcher":26,"roles":3843,"affiliations":3844,"properties":3855},"e2a4a93f-2c30-4e48-b062-51a68875c1fd",[],[3845],{"id":3846,"sortIndex":36,"affiliation":3847,"properties":26},"db558ce6-fb4e-40bb-baed-f841c25bfe15",{"id":3848,"createTime":3849,"updateTime":3849,"relativeEntities":3850,"slug":3851,"properties":3852,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"c9a91c20-7613-48e1-a445-9b670bc46856","2024-11-27T14:14:08.510+00:00",[],"Department-of-Periodontology-Dental-Institute-Guy-s-Hospital-King-s-College-London-London-United-Kingdom",{"title":3853},{"EN":3854},"Department of Periodontology, Dental Institute, Guy's Hospital, King's College London, London, United Kingdom",{"openalex":3856,"orcid":3858,"title":3860},{"VOID":3857},"A5023406605",{"VOID":3859},"https:\u002F\u002Forcid.org\u002F0000-0001-9073-8962",{"EN":3861},"Francis J. Hughes",{"id":3863,"sortIndex":36,"researcher":26,"roles":3864,"affiliations":3865,"properties":3872},"07d683f6-e4df-41a1-9549-ad4843f992bd",[],[3866],{"id":3867,"sortIndex":36,"affiliation":3868,"properties":26},"56b3028d-a0c8-4a2a-82eb-7bf416d7556b",{"id":3848,"createTime":3849,"updateTime":3849,"relativeEntities":3869,"slug":3851,"properties":3870,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":3871},{"EN":3854},{"openalex":3873,"orcid":3875,"title":3877},{"VOID":3874},"A5083851949",{"VOID":3876},"https:\u002F\u002Forcid.org\u002F0009-0002-9379-3929",{"EN":3878},"Borzo Gharibi",{"url":26,"publisher":3880,"properties":3905},{"id":659,"createTime":660,"updateTime":661,"relativeEntities":3881,"slug":663,"properties":3882,"entityType":24,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"subjectFields":3888,"manageAffiliations":3889,"indexDatabases":3890,"url":762,"thumbnailPath":26,"statistic":26,"gsStatistic":26,"type":26,"analyzePriority":26},[],{"country":3883,"issn":3884,"introduce":3885,"eissn":3886,"title":3887},{"VOID":666},{"VOID":668},{"EN":670},{"VOID":672},{"EN":674},[],[],[3891,3898],{"id":742,"indexDatabase":3892,"url":755,"indexYears":756,"academicFieldIds":3897,"indexDatabaseRanking":761},{"id":744,"createTime":745,"updateTime":746,"relativeEntities":3893,"label":3894,"description":3895,"key":752,"publicationTags":3896,"standard":26},[],{"EN":749,"VI":749},{"EN":749,"VI":751},[754],[758,759,760],{"id":723,"indexDatabase":3899,"url":738,"indexYears":26,"academicFieldIds":3904,"indexDatabaseRanking":26},{"id":725,"createTime":726,"updateTime":727,"relativeEntities":3900,"label":3901,"description":3902,"key":734,"publicationTags":3903,"standard":26},[],{"EN":730,"VI":730},{"VI":732,"EN":733},[736,737],[740],{"volume":3906,"pages":3907,"issue":3909},{"VOID":906},{"VOID":3908},"771-782",{"VOID":3910},"11",190,{"total":3911,"publishYear":26,"statisticByYear":3913},{"2013":103,"2014":241,"2015":116,"2016":124,"2017":53,"2018":103,"2019":234,"2020":222,"2021":234,"2022":336,"2023":51,"2024":158},"2012-11-01",[3916,3918,3922,3926,3929,3933,3937,3939,3942,3946,3950,3952,3956,3960,3964,3968,3972,3976,3980,3984,3988,3992,3996,4000,4004,4008,4012,4016,4020,4024,4028,4032,4036,4040,4044,4046,4049],{"id":26,"text":2394,"url":26,"identifiers":3917},{"doi":2396},{"id":26,"text":3919,"url":26,"identifiers":3920},"Horwitz, 2002, Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone, Proc Natl Acad Sci USA, 99, 8932, 10.1073\u002Fpnas.132252399",{"doi":3921},"10.1073\u002Fpnas.132252399",{"id":26,"text":3923,"url":26,"identifiers":3924},"Quarto, 2001, Repair of large bone defects with the use of autologous bone marrow stromal cells, N Engl J Med, 344, 385, 10.1056\u002FNEJM200102013440516",{"doi":3925},"10.1056\u002FNEJM200102013440516",{"id":26,"text":3927,"url":26,"identifiers":3928},"Hernigou, 2005, Percutaneous autologous bone-marrow grafting for nonunions. Influence of the number and concentration of progenitor cells, J Bone Joint Surg Am, 87, 1430",{},{"id":26,"text":3930,"url":26,"identifiers":3931},"Lee, 2010, Successful reconstruction of 15-cm segmental defects by bone marrow stem cells and resected autogenous bone graft in central hemangioma, J Oral Maxillofac Surg, 68, 188, 10.1016\u002Fj.joms.2009.08.031",{"doi":3932},"10.1016\u002Fj.joms.2009.08.031",{"id":26,"text":3934,"url":26,"identifiers":3935},"Mesimäki, 2009, Novel maxillary reconstruction with ectopic bone formation by GMP adipose stem cells, Int J Oral Maxillofac Surg, 38, 201, 10.1016\u002Fj.ijom.2009.01.001",{"doi":3936},"10.1016\u002Fj.ijom.2009.01.001",{"id":26,"text":2471,"url":26,"identifiers":3938},{"doi":2473},{"id":26,"text":3940,"url":26,"identifiers":3941},"Behre, 2009, Reply to “The correlation between cotransplantation of mesenchymal stem cells, higher recurrence rates in hematologic malignancy patients: Outcome of a pilot clinical study” by Ning et al, Leukemia, 178, 21579",{},{"id":26,"text":3943,"url":26,"identifiers":3944},"Timmers, 2011, Human mesenchymal stem cell-conditioned medium improves cardiac function following myocardial infarction, Stem Cell Res, 6, 206, 10.1016\u002Fj.scr.2011.01.001",{"doi":3945},"10.1016\u002Fj.scr.2011.01.001",{"id":26,"text":3947,"url":26,"identifiers":3948},"Amado, 2005, Cardiac repair with intramyocardial injection of allogeneic mesenchymal stem cells after myocardial infarction, Proc Natl Acad Sci USA, 102, 11474, 10.1073\u002Fpnas.0504388102",{"doi":3949},"10.1073\u002Fpnas.0504388102",{"id":26,"text":3755,"url":26,"identifiers":3951},{"doi":3757},{"id":26,"text":3953,"url":26,"identifiers":3954},"Tfilin, 2010, Mesenchymal stem cells increase hippocampal neurogenesis and counteract depressive-like behavior, Mol Psychiatry, 15, 1164, 10.1038\u002Fmp.2009.110",{"doi":3955},"10.1038\u002Fmp.2009.110",{"id":26,"text":3957,"url":26,"identifiers":3958},"Dwyer, 2010, Advances in mesenchymal stem cell-mediated gene therapy for cancer, Stem Cell Res Ther, 1, 25, 10.1186\u002Fscrt25",{"doi":3959},"10.1186\u002Fscrt25",{"id":26,"text":3961,"url":26,"identifiers":3962},"Bernardo, 2007, Optimization of in vitro expansion of human multipotent mesenchymal stromal cells for cell-therapy approaches: Further insights in the search for a fetal calf serum substitute, J Cell Physiol, 211, 121, 10.1002\u002Fjcp.20911",{"doi":3963},"10.1002\u002Fjcp.20911",{"id":26,"text":3965,"url":26,"identifiers":3966},"Sotiropoulou, 2006, Characterization of the optimal culture conditions for clinical scale production of human mesenchymal stem cells, Stem Cells, 24, 462, 10.1634\u002Fstemcells.2004-0331",{"doi":3967},"10.1634\u002Fstemcells.2004-0331",{"id":26,"text":3969,"url":26,"identifiers":3970},"Both, 2007, A rapid and efficient method for expansion of human mesenchymal stem cells, Tissue Eng, 13, 3, 10.1089\u002Ften.2005.0513",{"doi":3971},"10.1089\u002Ften.2005.0513",{"id":26,"text":3973,"url":26,"identifiers":3974},"Tsutsumi, 2001, Retention of multilineage differentiation potential of mesenchymal cells during proliferation in response to FGF, Biochem Biophys Res Commun, 288, 413, 10.1006\u002Fbbrc.2001.5777",{"doi":3975},"10.1006\u002Fbbrc.2001.5777",{"id":26,"text":3977,"url":26,"identifiers":3978},"Solchaga, 2005, FGF-2 enhances the mitotic and chondrogenic potentials of human adult bone marrow-derived mesenchymal stem cells, J Cell Physiol, 203, 398, 10.1002\u002Fjcp.20238",{"doi":3979},"10.1002\u002Fjcp.20238",{"id":26,"text":3981,"url":26,"identifiers":3982},"Martin, 1997, Fibroblast growth factor-2 supports ex vivo expansion and maintenance of osteogenic precursors from human bone marrow, Endocrinology, 138, 4456, 10.1210\u002Fendo.138.10.5425",{"doi":3983},"10.1210\u002Fendo.138.10.5425",{"id":26,"text":3985,"url":26,"identifiers":3986},"Bianchi, 2003, Ex vivo enrichment of mesenchymal cell progenitors by fibroblast growth factor 2, Exp Cell Res, 287, 98, 10.1016\u002FS0014-4827(03)00138-1",{"doi":3987},"10.1016\u002FS0014-4827(03)00138-1",{"id":26,"text":3989,"url":26,"identifiers":3990},"Tamama, 2006, Epidermal growth factor as a candidate for ex vivo expansion of bone marrow–derived mesenchymal stem cells, Stem Cells, 24, 686, 10.1634\u002Fstemcells.2005-0176",{"doi":3991},"10.1634\u002Fstemcells.2005-0176",{"id":26,"text":3993,"url":26,"identifiers":3994},"Pricola, 2009, Interleukin-6 maintains bone marrow-derived mesenchymal stem cell stemness by an ERK1\u002F2-dependent mechanism, J Cell Biochem, 108, 577, 10.1002\u002Fjcb.22289",{"doi":3995},"10.1002\u002Fjcb.22289",{"id":26,"text":3997,"url":26,"identifiers":3998},"Kumar, 2010, Platelet-derived growth factor receptor signaling is not involved in osteogenic differentiation of human mesenchymal stem cells, Tissue Eng Part A, 16, 983, 10.1089\u002Ften.tea.2009.0230",{"doi":3999},"10.1089\u002Ften.tea.2009.0230",{"id":26,"text":4001,"url":26,"identifiers":4002},"Gharibi, 2011, Adenosine receptor subtype expression and activation influence the differentiation of mesenchymal stem cells to osteoblasts and adipocytes, J Bone Miner Res, 26, 2112, 10.1002\u002Fjbmr.424",{"doi":4003},"10.1002\u002Fjbmr.424",{"id":26,"text":4005,"url":26,"identifiers":4006},"Neubauer, 2004, Basic fibroblast growth factor enhances PPARgamma ligand-induced adipogenesis of mesenchymal stem cells, FEBS Lett, 577, 277, 10.1016\u002Fj.febslet.2004.10.020",{"doi":4007},"10.1016\u002Fj.febslet.2004.10.020",{"id":26,"text":4009,"url":26,"identifiers":4010},"Ito, 2008, FGF-2 increases osteogenic and chondrogenic differentiation potentials of human mesenchymal stem cells by inactivation of TGF-β signaling, Cytotechnology, 56, 1, 10.1007\u002Fs10616-007-9092-1",{"doi":4011},"10.1007\u002Fs10616-007-9092-1",{"id":26,"text":4013,"url":26,"identifiers":4014},"Lai, 2011, Fibroblast growth factor 2 (Fgf2) inhibits differentiation of mesenchymal stem cells by inducing Twist2 and Spry4, blocking extracellular regulated kinase activation, and altering Fgf receptor expression levels, Stem Cells, 29, 1102, 10.1002\u002Fstem.661",{"doi":4015},"10.1002\u002Fstem.661",{"id":26,"text":4017,"url":26,"identifiers":4018},"Osathanon, 2011, Basic fibroblast growth factor inhibits mineralization but induces neuronal differentiation by human dental pulp stem cells through a FGFR and PLCγ signaling pathway, J Cell Biochem, 112, 1807, 10.1002\u002Fjcb.23097",{"doi":4019},"10.1002\u002Fjcb.23097",{"id":26,"text":4021,"url":26,"identifiers":4022},"Hayflick, 1961, The serial cultivation of human diploid cell strains, Exp Cell Res, 25, 585, 10.1016\u002F0014-4827(61)90192-6",{"doi":4023},"10.1016\u002F0014-4827(61)90192-6",{"id":26,"text":4025,"url":26,"identifiers":4026},"Bonab, 2006, Aging of mesenchymal stem cell in vitro, BMC Cell Biol, 7, 14, 10.1186\u002F1471-2121-7-14",{"doi":4027},"10.1186\u002F1471-2121-7-14",{"id":26,"text":4029,"url":26,"identifiers":4030},"Alves, 2010, A link between the accumulation of DNA damage and loss of multi-potency of human mesenchymal stromal cells, J Cell Mol Med, 14, 2729, 10.1111\u002Fj.1582-4934.2009.00931.x",{"doi":4031},"10.1111\u002Fj.1582-4934.2009.00931.x",{"id":26,"text":4033,"url":26,"identifiers":4034},"Galderisi, 2009, In vitro senescence of rat mesenchymal stem cells is accompanied by downregulation of stemness-related and DNA damage repair genes, Stem Cells Dev, 18, 1033, 10.1089\u002Fscd.2008.0324",{"doi":4035},"10.1089\u002Fscd.2008.0324",{"id":26,"text":4037,"url":26,"identifiers":4038},"Cheng, 2011, Replicative senescence of human bone marrow and umbilical cord derived mesenchymal stem cells and their differentiation to adipocytes and osteoblasts, Mol Biol Rep, 38, 5161, 10.1007\u002Fs11033-010-0665-2",{"doi":4039},"10.1007\u002Fs11033-010-0665-2",{"id":26,"text":4041,"url":26,"identifiers":4042},"Chamberlain, 2007, Concise review: Mesenchymal stem cells: Their phenotype, differentiation capacity, immunological features, and potential for homing, Stem Cells, 25, 2739, 10.1634\u002Fstemcells.2007-0197",{"doi":4043},"10.1634\u002Fstemcells.2007-0197",{"id":26,"text":966,"url":26,"identifiers":4045},{"doi":968},{"id":26,"text":4047,"url":26,"identifiers":4048},"Flores-Torales, 2010, The CD271 expression could be alone for establisher phenotypic marker in bone marrow derived mesenchymal stem cells, Folia Histochem Cytobiol, 48, 682",{},{"id":26,"text":1985,"url":26,"identifiers":4050},{"doi":1987},{"id":4052,"createTime":4053,"updateTime":4054,"relativeEntities":4055,"slug":4056,"properties":4057,"entityType":792,"verifyStatus":25,"verifyTime":4053,"verifyNote":793,"syncStatus":28,"languages":4075,"translateLanguages":4076,"viewCount":36,"primaryUrl":4077,"fullTextUrl":26,"authors":4078,"publicationType":877,"publisherRelationship":4153,"citationCount":4184,"citationInfo":4185,"publishDate":4187,"publishYear":4188,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":4189,"isForceReanalyzing":1210},"c6b62dc8-011e-4079-9196-ef8747dd1fbe","2024-10-15T11:02:10.066+00:00","2025-02-22T15:16:43.893+00:00",[],"Concise-Review-Growth-Differentiation-Factor-15-in-Pathology-A-Clinical-Role-",{"mag":4058,"keywords":4060,"pmc":4061,"openalex":4063,"abstract":4065,"title":4068,"pm":4071,"doi":4073},{"VOID":4059},"1995550877",{"VI":777},{"VOID":4062},"3841089",{"VOID":4064},"W1995550877",{"EN":4066,"VI":4067},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>Growth differentiation factor 15 (GDF15) is a divergent member of the transforming growth factor β family discovered in a broad range of cells, as indicated by the diversity of its nomenclature. However, the only tissue that expresses a high amount of GDF15 in the physiologic state is placenta. GDF15 is easily detected in blood, and its concentration varies with age. In fact, increased blood concentration of GDF15 is associated with numerous pathological conditions. However, the biological significance underlying these observations is far from clear. GDF15 could have a positive or negative role depending on the state of cells or their environment. Furthermore, study of its biology is hampered by lack of knowledge of its receptor and thus the signaling pathways that drive its action. GDF15 seems to be an integrative signal in pathologic conditions, giving information on severity of disease. Its effectiveness in classifying patients to modulate treatment remains to be shown. Development of therapeutic interventions with GDF15 or anti-GDF15 agents remains difficult until we uncover the mechanism that drives its activity.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\n               \u003Cjats:p>Yếu tố phân hóa tăng trưởng 15 (GDF15) là một thành viên khác biệt của họ yếu tố tăng trưởng biến đổi β, được phát hiện trong nhiều loại tế bào, như được chỉ ra bởi sự đa dạng trong việc đặt tên của nó. Tuy nhiên, mô duy nhất thể hiện một lượng lớn GDF15 trong trạng thái sinh lý là nhau thai. GDF15 dễ dàng được phát hiện trong máu, và nồng độ của nó thay đổi theo độ tuổi. Trên thực tế, nồng độ GDF15 trong máu tăng cao liên quan đến nhiều tình trạng bệnh lý. Tuy nhiên, ý nghĩa sinh học cơ sở cho những quan sát này vẫn chưa rõ ràng. GDF15 có thể đóng vai trò tích cực hoặc tiêu cực tùy thuộc vào trạng thái của tế bào hoặc môi trường của chúng. Hơn nữa, việc nghiên cứu sinh học của nó gặp khó khăn do thiếu kiến thức về thụ thể và do đó các con đường tín hiệu điều khiển hoạt động của nó. GDF15 dường như là một tín hiệu tích hợp trong các tình trạng bệnh lý, cung cấp thông tin về mức độ nghiêm trọng của bệnh. Hiệu quả của nó trong việc phân loại bệnh nhân để điều chỉnh điều trị vẫn cần được chứng minh. Việc phát triển các can thiệp trị liệu với GDF15 hoặc các tác nhân chống GDF15 vẫn gặp nhiều khó khăn cho đến khi chúng ta khám phá được cơ chế điều khiển hoạt động của nó.\u003C\u002Fjats:p>",{"EN":4069,"VI":4070},"Concise Review: Growth Differentiation Factor 15 in Pathology: A Clinical Role?","Đánh Giá Ngắn Gọn: Yếu Tố Phân Hóa Tăng Trưởng 15 Trong Bệnh Lý: Vai Trò Lâm Sàng?",{"VOID":4072},"24191265",{"VOID":4074},"10.5966\u002Fsctm.2013-0055",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F2\u002F12\u002F946-952\u002F6395248",[4079,4099,4121],{"id":4080,"sortIndex":115,"researcher":26,"roles":4081,"affiliations":4082,"properties":4094},"f7bebb46-dca3-4351-afeb-c815cbd7f029",[],[4083],{"id":4084,"sortIndex":36,"affiliation":4085,"properties":26},"fee0e966-f477-4fd5-9357-52f064ac1f7c",{"id":4086,"createTime":4087,"updateTime":4088,"relativeEntities":4089,"slug":4090,"properties":4091,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"c5655e76-ff85-4796-979b-490eb8356ee4","2023-12-07T21:51:47.848+00:00","2024-10-15T11:02:10.164+00:00",[],"Hematology-Department-University-Hospital-Purpan-Toulouse-France-",{"title":4092},{"VI":4093},"Hematology Department, University Hospital Purpan, Toulouse, 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2009, Growth differentiation factor 15 production is necessary for normal erythroid differentiation and is increased in refractory anaemia with ring-sideroblasts, Br J Haematol, 144, 251, 10.1111\u002Fj.1365-2141.2008.07441.x",{"doi":4386},"10.1111\u002Fj.1365-2141.2008.07441.x",{"id":26,"text":4388,"url":26,"identifiers":4389},"Finkenstedt, 2009, Regulation of iron metabolism through GDF15 and hepcidin in pyruvate kinase deficiency, Br J Haematol, 144, 789, 10.1111\u002Fj.1365-2141.2008.07535.x",{"doi":4390},"10.1111\u002Fj.1365-2141.2008.07535.x",{"id":26,"text":4392,"url":26,"identifiers":4393},"Bruns, 2012, Multiple myeloma-related deregulation of bone marrow-derived CD34+ hematopoietic stem and progenitor cells, Blood, 120, 2620, 10.1182\u002Fblood-2011-04-347484",{"doi":4394},"10.1182\u002Fblood-2011-04-347484",{"id":26,"text":4396,"url":26,"identifiers":4397},"Brown, 2002, Concentration in plasma of macrophage inhibitory cytokine-1 and risk of cardiovascular events in women: A nested case-control study, Lancet, 359, 2159, 10.1016\u002FS0140-6736(02)09093-1",{"doi":4398},"10.1016\u002FS0140-6736(02)09093-1",{"id":26,"text":4400,"url":26,"identifiers":4401},"Kempf, 2007, Prognostic utility of growth differentiation factor-15 in patients with chronic heart failure, J Am Coll Cardiol, 50, 1054, 10.1016\u002Fj.jacc.2007.04.091",{"doi":4402},"10.1016\u002Fj.jacc.2007.04.091",{"id":26,"text":4404,"url":26,"identifiers":4405},"Kempf, 2007, Growth-differentiation factor-15 improves risk stratification in ST-segment elevation myocardial infarction, Eur Heart J, 28, 2858, 10.1093\u002Feurheartj\u002Fehm465",{"doi":4406},"10.1093\u002Feurheartj\u002Fehm465",{"id":26,"text":4408,"url":26,"identifiers":4409},"Wollert, 2007, Prognostic value of growth-differentiation factor-15 in patients with non-ST-elevation acute coronary syndrome, Circulation, 115, 962, 10.1161\u002FCIRCULATIONAHA.106.650846",{"doi":4410},"10.1161\u002FCIRCULATIONAHA.106.650846",{"id":26,"text":4412,"url":26,"identifiers":4413},"Lankeit, 2008, Growth differentiation factor-15 for prognostic assessment of patients with acute pulmonary embolism, Am J Respir Crit Care Med, 177, 1018, 10.1164\u002Frccm.200712-1786OC",{"doi":4414},"10.1164\u002Frccm.200712-1786OC",{"id":26,"text":4416,"url":26,"identifiers":4417},"Nickel, 2008, Growth differentiation factor-15 in idiopathic pulmonary arterial hypertension, Am J Respir Crit Care Med, 178, 534, 10.1164\u002Frccm.200802-235OC",{"doi":4418},"10.1164\u002Frccm.200802-235OC",{"id":26,"text":4420,"url":26,"identifiers":4421},"Foley, 2009, Growth differentiation factor-15 predicts mortality and morbidity after cardiac resynchronization therapy, Eur Heart J, 30, 2749, 10.1093\u002Feurheartj\u002Fehp300",{"doi":4422},"10.1093\u002Feurheartj\u002Fehp300",{"id":26,"text":4424,"url":26,"identifiers":4425},"Norozi, 2011, Growth differentiation factor 15: An additional diagnostic tool for the risk stratification of developing heart failure in patients with operated congenital heart defects?, Am Heart J, 162, 131, 10.1016\u002Fj.ahj.2011.03.036",{"doi":4426},"10.1016\u002Fj.ahj.2011.03.036",{"id":26,"text":4428,"url":26,"identifiers":4429},"Wollert, 2012, Growth differentiation factor 15 in heart failure: An update, Curr Heart Fail Rep, 9, 337, 10.1007\u002Fs11897-012-0113-9",{"doi":4430},"10.1007\u002Fs11897-012-0113-9",{"id":26,"text":4432,"url":26,"identifiers":4433},"Johnen, 2012, Increased expression of the TGF-b superfamily cytokine MIC-1\u002FGDF15 protects ApoE(−\u002F−) mice from the development of atherosclerosis, Cardiovasc Pathol, 21, 499, 10.1016\u002Fj.carpath.2012.02.003",{"doi":4434},"10.1016\u002Fj.carpath.2012.02.003",{"id":26,"text":4436,"url":26,"identifiers":4437},"Bonaterra, 2012, Growth differentiation factor-15 deficiency inhibits atherosclerosis progression by regulating interleukin-6-dependent inflammatory response to vascular injury, J Am Heart Assoc, 1, e002550, 10.1161\u002FJAHA.112.002550",{"doi":4438},"10.1161\u002FJAHA.112.002550",{"id":26,"text":4440,"url":26,"identifiers":4441},"Kempf, 2006, The transforming growth factor-beta superfamily member growth-differentiation factor-15 protects the heart from ischemia\u002Freperfusion injury, Circ Res, 98, 351, 10.1161\u002F01.RES.0000202805.73038.48",{"doi":4442},"10.1161\u002F01.RES.0000202805.73038.48",{"id":26,"text":4444,"url":26,"identifiers":4445},"Xu, 2011, Growth differentiation factor 15 in cardiovascular diseases: From bench to bedside, Biomarkers, 16, 466, 10.3109\u002F1354750X.2011.580006",{"doi":4446},"10.3109\u002F1354750X.2011.580006",{"id":26,"text":4448,"url":26,"identifiers":4449},"Brown, 2007, Serum macrophage inhibitory cytokine 1 in rheumatoid arthritis. A potential marker of erosive joint destruction, Arthritis Rheum, 56, 753, 10.1002\u002Fart.22410",{"doi":4450},"10.1002\u002Fart.22410",{"id":26,"text":4452,"url":26,"identifiers":4453},"Breit, 2012, Macrophage inhibitory cytokine-1 (MIC-1\u002FGDF15) and mortality in end-stage renal disease, Nephrol Dial Transplant, 27, 70, 10.1093\u002Fndt\u002Fgfr575",{"doi":4454},"10.1093\u002Fndt\u002Fgfr575",{"id":26,"text":4456,"url":26,"identifiers":4457},"Hellemons, 2012, Growth-differentiation factor 15 predicts worsening of albuminuria in patients with type 2 diabetes, Diabetes Care, 35, 2340, 10.2337\u002Fdc12-0180",{"doi":4458},"10.2337\u002Fdc12-0180",{"id":26,"text":4460,"url":26,"identifiers":4461},"Mensching, 2012, Local substitution of GDF-15 improves axonal and sensory recovery after peripheral nerve injury, Cell Tissue Res, 350, 225, 10.1007\u002Fs00441-012-1493-6",{"doi":4462},"10.1007\u002Fs00441-012-1493-6",{"id":26,"text":4464,"url":26,"identifiers":4465},"Hsiao, 2000, Characterization of growth-differentiation factor 15, a transforming growth factor beta superfamily member induced following liver injury, Mol Cell Biol, 20, 3742, 10.1128\u002FMCB.20.10.3742-3751.2000",{"doi":4466},"10.1128\u002FMCB.20.10.3742-3751.2000",{"id":26,"text":4468,"url":26,"identifiers":4469},"Strelau, 2009, Progressive postnatal motoneuron loss in mice lacking GDF-15, J Neurosci, 29, 13640, 10.1523\u002FJNEUROSCI.1133-09.2009",{"doi":4470},"10.1523\u002FJNEUROSCI.1133-09.2009",{"id":4472,"createTime":4473,"updateTime":4474,"relativeEntities":4475,"slug":4476,"properties":4477,"entityType":792,"verifyStatus":25,"verifyTime":4473,"verifyNote":793,"syncStatus":28,"languages":4495,"translateLanguages":4496,"viewCount":36,"primaryUrl":4497,"fullTextUrl":26,"authors":4498,"publicationType":877,"publisherRelationship":4838,"citationCount":628,"citationInfo":4870,"publishDate":4872,"publishYear":4873,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":4874,"isForceReanalyzing":1210},"1a5260b9-6660-4548-8474-28f275170015","2024-10-01T09:56:12.175+00:00","2025-02-22T15:17:42.771+00:00",[],"Intranasal-delivery-of-mesenchymal-stem-cell-derived-extracellular-vesicles-exerts-immunomodulatory-and-neuroprotective-effects-in-a-3xTg-model-of-Alzheimer-s-disease",{"mag":4478,"keywords":4480,"pmc":4481,"openalex":4483,"abstract":4485,"title":4488,"pm":4491,"doi":4493},{"VOID":4479},"3029492181",{"VI":777},{"VOID":4482},"7445021",{"VOID":4484},"W3029492181",{"EN":4486,"VI":4487},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>The critical role of neuroinflammation in favoring and accelerating the pathogenic process in Alzheimer's disease (AD) increased the need to target the cerebral innate immune cells as a potential therapeutic strategy to slow down the disease progression. In this scenario, mesenchymal stem cells (MSCs) have risen considerable interest thanks to their immunomodulatory properties, which have been largely ascribed to the release of extracellular vesicles (EVs), namely exosomes and microvesicles. Indeed, the beneficial effects of MSC-EVs in regulating the inflammatory response have been reported in different AD mouse models, upon chronic intravenous or intracerebroventricular administration. In this study, we use the triple-transgenic 3xTg mice showing for the first time that the intranasal route of administration of EVs, derived from cytokine-preconditioned MSCs, was able to induce immunomodulatory and neuroprotective effects in AD. MSC-EVs reached the brain, where they dampened the activation of microglia cells and increased dendritic spine density. MSC-EVs polarized in vitro murine primary microglia toward an anti-inflammatory phenotype suggesting that the neuroprotective effects observed in transgenic mice could result from a positive modulation of the inflammatory status. The possibility to administer MSC-EVs through a noninvasive route and the demonstration of their anti-inflammatory efficacy might accelerate the chance of a translational exploitation of MSC-EVs in AD.\u003C\u002Fjats:p>\u003Cjats:sec>\u003Cjats:title\u002F>\u003Cjats:p>Significance statement In the attempt to find a possible cure for Alzheimer's disease (AD), mesenchymal stem cells (MSCs) and their derived extracellular vesicles (EVs) are being investigated for therapeutic purposes thanks to their protective and anti-inflammatory properties. The results from this study show that MSC-EVs operate in dampening inflammation (that favors and accelerates the pathogenic process in AD) and in inducing neuroprotective effects. Furthermore, they sustain the delivery of MSC-EVs through the intranasal route, being safe and low invasive, thus laying the foundation for a translational future exploitation of MSC-EVs toward therapy.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Vai trò quan trọng của tình trạng viêm thần kinh trong việc thúc đẩy và tăng cường quá trình bệnh lý trong bệnh Alzheimer (AD) đã làm gia tăng nhu cầu hướng đến các tế bào miễn dịch bẩm sinh trong não như một chiến lược điều trị tiềm năng nhằm làm chậm tiến trình của bệnh. Trong bối cảnh này, các tế bào gốc trung mô (MSCs) đã tạo ra sự quan tâm đáng kể nhờ vào các thuộc tính điều chỉnh miễn dịch của chúng, mà chủ yếu được cho là do sự giải phóng các vesicle ngoại bào (EVs), bao gồm các exosome và microvesicle. Thật vậy, những hiệu ứng có lợi của MSC-EVs trong việc điều chỉnh phản ứng viêm đã được báo cáo trong các mô hình chuột AD khác nhau sau khi tiêm truyền tĩnh mạch hoặc vào não thất kéo dài. Trong nghiên cứu này, chúng tôi sử dụng chuột 3xTg ba chuyển gen lần đầu tiên cho thấy rằng đường tiêm qua mũi cho các EVs, thu được từ MSCs đã được xử lý bằng cytokine, có khả năng tạo ra các hiệu ứng điều chỉnh miễn dịch và bảo vệ thần kinh trong AD. MSC-EVs đã đến não, nơi chúng làm giảm mức độ kích hoạt của các tế bào microglia và tăng mật độ gai dendrite. MSC-EVs đã làm phân cực các microglia chính murine in vitro về kiểu hình chống viêm, gợi ý rằng các hiệu ứng bảo vệ thần kinh quan sát được trong chuột chuyển gen có thể là kết quả của việc điều chỉnh tích cực tình trạng viêm. Khả năng tiêm MSC-EVs qua một lộ trình không xâm lấn và sự chứng minh hiệu quả chống viêm của chúng có thể tăng tốc khả năng khai thác chuyển giao của MSC-EVs trong AD.\u003C\u002Fjats:p>\u003Cjats:sec>\u003Cjats:title\u002F>\u003Cjats:p>Tuyên bố ý nghĩa Trong nỗ lực tìm kiếm một phương pháp điều trị khả thi cho bệnh Alzheimer (AD), các tế bào gốc trung mô (MSCs) và các vesicle ngoại bào (EVs) được chiết xuất từ chúng đang được nghiên cứu với mục đích điều trị nhờ vào các thuộc tính bảo vệ và chống viêm của chúng. Các kết quả từ nghiên cứu này cho thấy MSC-EVs hoạt động trong việc giảm viêm (khiến bệnh lý trong AD trở nên trầm trọng hơn và gia tăng tốc độ phát triển của bệnh) và trong việc tạo ra các hiệu ứng bảo vệ thần kinh. Hơn nữa, các mẫu cũng hỗ trợ việc giao nộp MSC-EVs qua đường mũi, là an toàn và ít xâm lấn, do đó mở ra nền tảng cho việc khai thác trong tương lai các MSC-EVs với mục đích điều trị.",{"EN":4489,"VI":4490},"Intranasal delivery of mesenchymal stem cell-derived extracellular vesicles exerts immunomodulatory and neuroprotective effects in a 3xTg model of Alzheimer's disease","Giao nộp nội bào ngoại bào của tế bào gốc trung mô mang lại hiệu ứng điều chỉnh miễn dịch và bảo vệ thần kinh trong mô hình 3xTg của bệnh Alzheimer",{"VOID":4492},"32496649",{"VOID":4494},"10.1002\u002Fsctm.19-0327",[102],[101],"https:\u002F\u002Facademic.oup.com\u002Fstcltm\u002Farticle\u002F9\u002F9\u002F1068\u002F6406935",[4499,4520,4535,4562,4593,4620,4641,4664,4681,4698,4715,4732,4753,4770,4787,4804,4821],{"id":4500,"sortIndex":135,"researcher":26,"roles":4501,"affiliations":4502,"properties":4513},"f2c50866-1354-4dde-86c2-c92dd982c1a3",[],[4503],{"id":4504,"sortIndex":36,"affiliation":4505,"properties":26},"16ead810-02d3-49c5-86f1-b59cbb040d5a",{"id":4506,"createTime":4507,"updateTime":4507,"relativeEntities":4508,"slug":4509,"properties":4510,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"b4d70f93-7155-4838-a9a1-17c9a5f8909b","2024-10-01T09:56:12.192+00:00",[],"1-School-of-Medicine-and-Surgery-University-of-Milano-Bicocca-Monza-Italy",{"title":4511},{"EN":4512},"1 School of Medicine and Surgery University of Milano-Bicocca, 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NeuroMI-Milan Center for Neuroscience University of Milano-Bicocca, Milano (MI), Italy",{"openalex":4556,"orcid":4558,"title":4560},{"VOID":4557},"A5046979142",{"VOID":4559},"https:\u002F\u002Forcid.org\u002F0000-0003-2832-6961",{"EN":4561},"Alessandra Bulbarelli",{"id":4563,"sortIndex":298,"researcher":26,"roles":4564,"affiliations":4565,"properties":4586},"f3786b73-b5e3-495b-8560-20fcbd63c67e",[],[4566,4576],{"id":4567,"sortIndex":115,"affiliation":4568,"properties":26},"93cd4812-a2dd-4dcc-8002-49f9cf2898b6",{"id":4569,"createTime":4570,"updateTime":4570,"relativeEntities":4571,"slug":4572,"properties":4573,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"e1fb1ad8-0ab0-42d8-91ac-cdf95136c2bb","2024-10-01T09:56:12.305+00:00",[],"7-Department-of-Biomedical-Sciences-Humanitas-University-Pieve-Emanuele-MI-Italy",{"title":4574},{"EN":4575},"7 Department of Biomedical Sciences Humanitas University, Pieve Emanuele (MI), Italy",{"id":4577,"sortIndex":36,"affiliation":4578,"properties":26},"910e2963-7095-4e8f-b210-986d8d977cf6",{"id":4579,"createTime":4580,"updateTime":4580,"relativeEntities":4581,"slug":4582,"properties":4583,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"a51a703e-f1af-439e-87f4-f0206a3ad4f7","2024-10-01T09:56:12.234+00:00",[],"3-Laboratory-of-Pharmacology-and-Brain-Pathology-Neuro-Center-Humanitas-Clinical-and-Research-Center-IRCCS-Rozzano-MI-Italy",{"title":4584},{"EN":4585},"3 Laboratory of Pharmacology and Brain Pathology, Neuro Center Humanitas Clinical and Research Center—IRCCS, Rozzano (MI), Italy",{"openalex":4587,"orcid":4589,"title":4591},{"VOID":4588},"A5048757910",{"VOID":4590},"https:\u002F\u002Forcid.org\u002F0000-0002-3569-7843",{"EN":4592},"Michela 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10.1016\u002Fj.jconrel.2015.03.033",{"doi":5296},"10.1016\u002Fj.jconrel.2015.03.033",{"id":5298,"createTime":5299,"updateTime":5300,"relativeEntities":5301,"slug":5302,"properties":5303,"entityType":792,"verifyStatus":25,"verifyTime":5299,"verifyNote":793,"syncStatus":28,"languages":5320,"translateLanguages":5321,"viewCount":36,"primaryUrl":5322,"fullTextUrl":26,"authors":5323,"publicationType":877,"publisherRelationship":5517,"citationCount":5550,"citationInfo":5551,"publishDate":5553,"publishYear":5554,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":5555,"isForceReanalyzing":1210},"22474a09-2d84-4aa3-b838-5446fbb6b40d","2024-10-01T09:54:54.179+00:00","2025-02-22T15:18:40.112+00:00",[],"Intranasal-Administration-of-Extracellular-Vesicles-Derived-from-Human-Teeth-Stem-Cells-Improves-Motor-Symptoms-and-Normalizes-Tyrosine-Hydroxylase-Expression-in-the-Substantia-Nigra-and-Striatum-of-the-6-Hydroxydopamine-Treated-Rats",{"mag":5304,"keywords":5306,"pmc":5307,"openalex":5309,"abstract":5311,"title":5314,"pm":5317,"doi":5319},{"VOID":5305},"2914375886",{"VI":777},{"VOID":5308},"6477008",{"VOID":5310},"W2914375886",{"EN":5312,"VI":5313},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>Parkinson's disease (PD) is the second most common neurodegenerative disorder affecting millions of people worldwide. At present, there is no effective cure for PD; treatments are symptomatic and do not halt progression of neurodegeneration. Extracellular vesicles (EVs) can cross the blood–brain barrier and represent promising alternative to the classical treatment strategies. In the present study, we examined therapeutic effects of intranasal administration of EVs derived from human exfoliated deciduous teeth stem cells (SHEDs) on unilateral 6-hydroxydopamine (6-OHDA) medial forebrain bundle (MFB) rat model of PD. CatWalk gait tests revealed that EVs effectively suppressed 6-OHDA-induced gait impairments. All tested gait parameters (stand, stride length, step cycle, and duty cycle) were significantly improved in EV-treated animals when compared with 6-OHDA-lesion group rats. Furthermore, EVs slowed down numbers of 6-OHDA-induced contralateral rotations in apomorphine test. Improvements in motor function correlated with normalization of tyrosine hydroxylase expression in the striatum and substantia nigra. In conclusion, we demonstrated, for the first time, the therapeutic efficacy of intranasal administration of EVs derived from SHEDs in a rat model of PD induced by 6-OHDA intra-MFB lesion. Our findings could be potentially exploited for the development of new treatment strategies against PD.\u003C\u002Fjats:p>\n               \u003Cjats:sec>\n                  \u003Cjats:title \u002F>\n               \u003C\u002Fjats:sec>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\n               \u003Cjats:p>Bệnh Parkinson (PD) là rối loạn thoái hóa thần kinh phổ biến thứ hai, ảnh hưởng đến hàng triệu người trên toàn thế giới. Hiện tại, không có phương pháp chữa trị hiệu quả cho PD; các phương pháp điều trị hiện có chỉ nhằm giải quyết triệu chứng mà không làm ngừng tiến triển của sự thoái hóa thần kinh. Các vesicle ngoại bào (EVs) có khả năng vượt qua hàng rào máu-não và thể hiện tiềm năng như một liệu pháp thay thế đáng hứa hẹn so với các chiến lược điều trị cổ điển. Trong nghiên cứu này, chúng tôi đã xem xét tác dụng điều trị của việc đưa EVs qua đường mũi, có nguồn gốc từ tế bào gốc từ răng sữa người (SHEDs), trên mô hình chuột mắc PD do 6-hydroxydopamine (6-OHDA) gây ra. Các thử nghiệm đi bộ CatWalk cho thấy rằng EVs đã hiệu quả trong việc làm giảm các vấn đề về đi lại do 6-OHDA gây ra. Tất cả các thông số đi bộ được thử nghiệm (thời gian đứng, độ dài bước, chu trình bước và chu trình hoạt động) đều được cải thiện đáng kể ở các động vật được điều trị bằng EVs so với nhóm chuột bị tổn thương ở 6-OHDA. Hơn nữa, EVs đã làm chậm số lần quay bên trái do 6-OHDA gây ra trong bài thử nghiệm apomorphine. Sự cải thiện trong chức năng vận động có liên quan đến sự bình thường hóa biểu hiện của tyrosine hydroxylase trong nhân đuôi và chất đen. Kết luận, chúng tôi đã chứng minh, lần đầu tiên, hiệu quả điều trị của việc đưa EVs qua đường mũi có nguồn gốc từ SHEDs trong mô hình chuột mắc PD do tổn thương intra-MFB bởi 6-OHDA gây ra. Những phát hiện của chúng tôi có thể được khai thác tiềm năng cho việc phát triển các chiến lược điều trị mới chống lại PD.",{"EN":5315,"VI":5316},"Intranasal Administration of Extracellular Vesicles Derived from Human Teeth Stem Cells Improves Motor Symptoms and Normalizes Tyrosine Hydroxylase Expression in the Substantia Nigra and Striatum of the 6-Hydroxydopamine-Treated Rats","Quản lý Môi trường Nước: Các Giải pháp Bền vững cho Tương 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