Photothermal nanofibers enable macromolecule delivery in unstimulated human T cells
Tài liệu tham khảo
Stewart, 2016, In vitro and ex vivo strategies for intracellular delivery, Nature, 538, 183, 10.1038/nature19764
Morshedi Rad, 2021, A Comprehensive Review on Intracellular Delivery, Adv. Mater., 33
Mitchell, 2021, Engineering precision nanoparticles for drug delivery, Nat. Rev. Drug Discov., 20, 101, 10.1038/s41573-020-0090-8
Butt, 2022, Appraisal for the potential of viral and nonviral vectors in gene therapy: a review, Genes, 13, 10.3390/genes13081370
Stewart, 2018, Intracellular delivery by membrane disruption: mechanisms, strategies, and concepts, Chem. Rev., 118, 7409, 10.1021/acs.chemrev.7b00678
Qu, 2020, Surface-mediated intracellular delivery by physical membrane disruption, ACS Appl. Mater. Interfaces, 12, 31054, 10.1021/acsami.0c06978
Sadelain, 2017, Therapeutic T cell engineering, Nature, 545, 423, 10.1038/nature22395
June, 2018, Chimeric antigen receptor therapy, New Engl. J. Med., 379, 64, 10.1056/NEJMra1706169
Moretti, 2022, The past, present, and future of non-viral CAR T cells, Front. Immunol., 13, 1, 10.3389/fimmu.2022.867013
Wagner, 2022, Review: sustainable clinical development of CAR-T Cells – Switching from viral transduction towards CRISPR-cas gene editing, Front. Immunol., 13, 1, 10.3389/fimmu.2022.865424
Labbé, 2021, Lentiviral vectors for T Cell engineering: clinical applications, bioprocessing and future perspectives, Viruses, 13, 1528, 10.3390/v13081528
DiTommaso, 2018, Cell engineering with microfluidic squeezing preserves functionality of primary immune cells in vivo, Proc. Nat. Acad. Sci., 115, E10907, 10.1073/pnas.1809671115
Joo, 2021, Highly efficient transfection of human primary T lymphocytes using droplet-enabled mechanoporation, ACS Nano, 15, 12888, 10.1021/acsnano.0c10473
Zhang, 2018, Optimized DNA electroporation for primary human T cell engineering, BMC Biotechnol, 18, 1, 10.1186/s12896-018-0419-0
Tay, 2019, Transfection with nanostructure electro-injection is minimally perturbative, Adv Ther (Weinh), 2
Cao, 2019, Nontoxic nanopore electroporation for effective intracellular delivery of biological macromolecules, Proc Natl Acad Sci USA., 116, 7899, 10.1073/pnas.1818553116
Zuvin, 2019, Magnetofection of green fluorescent protein encoding DNA-bearing polyethyleneimine-coated superparamagnetic iron oxide nanoparticles to human breast cancer cells, ACS Omega, 4, 12366, 10.1021/acsomega.9b01000
Xiong, 2014, Comparison of gold nanoparticle mediated photoporation: vapor nanobubbles outperform direct heating for delivering macromolecules in live cells, ACS Nano, 8, 6288, 10.1021/nn5017742
Tang, 2021, Ultrahigh efficiency and minimalist intracellular delivery of macromolecules mediated by latent-photothermal surfaces, ACS Appl Mater Interfaces, 13, 12594, 10.1021/acsami.0c22736
Xiong, 2016, Laser-assisted photoporation: fundamentals, technological advances and applications, Adv Phys X, 1, 596
Xiong, 2023, Photothermal nanomaterial-mediated photoporation, Acc. Chem. Res., 56, 631, 10.1021/acs.accounts.2c00770
Ramon, 2021, Vapor nanobubble-mediated photoporation constitutes a versatile intracellular delivery technology, Curr. Opin. Colloid Interface Sci., 54, 10.1016/j.cocis.2021.101453
Lapotko, 2009, Plasmonic nanoparticle-generated photothermal bubbles and their biomedical applications, Nanomedicine, 4, 813, 10.2217/nnm.09.59
Lukianova-Hleb, 2010, Plasmonic nanobubbles as transient vapor nanobubbles generated around plasmonic nanoparticles, ACS Nano., 4, 2109, 10.1021/nn1000222
Maheshwari, 2018, Dynamics of formation of a vapor nanobubble around a heated nanoparticle, J. Phys. Chem. C, 122, 20571, 10.1021/acs.jpcc.8b04017
Wayteck, 2017, Comparing photoporation and nucleofection for delivery of small interfering RNA to cytotoxic T cells, J. Control. Release, 267, 154, 10.1016/j.jconrel.2017.08.002
Raes, 2019, Gold Nanoparticle-mediated photoporation enables delivery of macromolecules over a wide range of molecular weights in human CD4+ T Cells, Crystals, 9, 411, 10.3390/cryst9080411
Raes, 2021, Cas9 RNP transfection by vapor nanobubble photoporation for ex vivo cell engineering, Mol. Ther. Nucl. Acids, 25, 696, 10.1016/j.omtn.2021.08.014
Wang, 2018, Using porous magnetic iron oxide nanomaterials as a facile photoporation nanoplatform for macromolecular delivery, J. Mater. Chem. B, 6, 4427, 10.1039/C8TB01026A
Harizaj, 2021, Nanoparticle-sensitized photoporation enables inflammasome activation studies in targeted single cells, Nanoscale, 13, 6592, 10.1039/D0NR05067A
Chakravarty, 2010, Delivery of molecules into cells using carbon nanoparticles activated by femtosecond laser pulses, Nat Nanotechnol, 5, 607, 10.1038/nnano.2010.126
Sengupta, 2014, Efficient intracellular delivery of molecules with high cell viability using nanosecond-pulsed laser-activated carbon nanoparticles, ACS Nano, 8, 2889, 10.1021/nn500100x
Chakravarty, 2016, Parameters affecting intracellular delivery of molecules using laser-activated carbon nanoparticles, Nanomedicine, 12, 1003, 10.1016/j.nano.2015.12.380
Liu, 2020, Surface functionalization with polyethylene glycol and polyethyleneimine improves the performance of graphene-based materials for safe and efficient intracellular delivery by laser-induced photoporation, Int. J. Mol. Sci., 21, 1540, 10.3390/ijms21041540
Liu, 2018, Repeated photoporation with graphene quantum dots enables homogeneous labeling of live cells with extrinsic markers for fluorescence microscopy, Light Sci. Appl., 7, 47, 10.1038/s41377-018-0048-3
Siegrist, 2019, Preclinical hazard evaluation strategy for nanomedicines, Nanotoxicology, 13, 73, 10.1080/17435390.2018.1505000
Foulkes, 2020, The regulation of nanomaterials and nanomedicines for clinical application: current and future perspectives, Biomater. Sci., 8, 4653, 10.1039/D0BM00558D
Xiong, 2021, Photothermal nanofibres enable safe engineering of therapeutic cells, Nat. Nanotechnol., 16, 1281, 10.1038/s41565-021-00976-3
Liu, 2011, Transfection optimization for primary human CD8+ cells, J. Immunol. Methods, 372, 22, 10.1016/j.jim.2011.06.026
Seki, 2018, Optimized RNP transfection for highly efficient CRI SPR/Cas9-mediated gene knockout in primary T cells, J. Exp. Med., 215, 985, 10.1084/jem.20171626
Aksoy, 2018, Viable and efficient electroporation-based genetic manipulation of unstimulated human T cells, BioRxiv
Howden, 2019, Quantitative analysis of T cell proteomes and environmental sensors during T cell differentiation, Nat Immunol., 20, 1542, 10.1038/s41590-019-0495-x
Wolf, 2020, Dynamics in protein translation sustaining T cell preparedness, Nat Immunol., 21, 927, 10.1038/s41590-020-0714-5
Robinson, 2017, Transcriptional regulation of T-cell lipid metabolism: implications for plasma membrane lipid rafts and T-cell function, Front Immunol, 8, 1, 10.3389/fimmu.2017.01636
Gattinoni, 2005, Acquisition of full effector function in vitro paradoxically impairs the in vivo antitumor efficacy of adoptively transferred CD8+ T cells, J. Clin. Invest., 115, 1616, 10.1172/JCI24480
Gumber, 2022, Improving CAR-T immunotherapy: overcoming the challenges of T cell exhaustion, EBioMedicine, 77, 10.1016/j.ebiom.2022.103941
Klebanoff, 2005, Central memory self/tumor-reactive CD8+ T cells confer superior antitumor immunity compared with effector memory T cells, Proc. Natl. Acad. Sci. U S A, 102, 9571, 10.1073/pnas.0503726102
Hinrichs, 2009, Adoptively transferred effector cells derived from naïve rather than central memory CD8 + T cells mediate superior antitumor immunity, Proc. Natl. Acad. Sci., 106, 17469, 10.1073/pnas.0907448106
Gattinoni, 2011, A human memory T cell subset with stem cell–like properties, Nat. Med., 17, 1290, 10.1038/nm.2446
Fraietta, 2018, Disruption of TET2 promotes the therapeutic efficacy of CD19-targeted T cells, Nature, 558, 307, 10.1038/s41586-018-0178-z
Fraietta, 2018, Determinants of response and resistance to CD19 chimeric antigen receptor (CAR) T cell therapy of chronic lymphocytic leukemia, Nat. Med., 24, 563, 10.1038/s41591-018-0010-1
Arcangeli, 2020, Next-generation manufacturing protocols enriching TSCM CAR T Cells can overcome disease-specific T Cell defects in cancer patients, Front. Immunol., 11, 10.3389/fimmu.2020.01217
Ghassemi, 2018, Reducing ex vivo culture improves the antileukemic activity of chimeric antigen receptor (CAR) T cells, Cancer Immunol. Res., 6, 1100, 10.1158/2326-6066.CIR-17-0405
de Macedo Abdo, 2020, Development of CAR-T cell therapy for B-ALL using a point-of-care approach, Oncoimmunology, 9, 10.1080/2162402X.2020.1752592
Ghassemi, 2022, Rapid manufacturing of non-activated potent CAR T cells, Nat. Biomed. Eng., 6, 118, 10.1038/s41551-021-00842-6
Schindelin, 2012, Fiji: an open-source platform for biological-image analysis, Nat. Methods, 9, 676, 10.1038/nmeth.2019
Houthaeve, 2018, Targeted perturbation of nuclear envelope integrity with vapor nanobubble-mediated photoporation, ACS Nano, 12, 7791, 10.1021/acsnano.8b01860
Bolea-Fernandez, 2017, Overcoming spectral overlap via inductively coupled plasma-tandem mass spectrometry (ICP-MS/MS). A tutorial review, J. Anal. At Spectrom., 32, 1660, 10.1039/C7JA00010C
Harizaj, 2021, Photoporation with biodegradable polydopamine nanosensitizers enables safe and efficient delivery of mRNA in human T Cells, Adv Funct Mater, 31, 10.1002/adfm.202102472
Berdecka, 2023, Delivery of macromolecules in unstimulated T cells by photoporation with polydopamine nanoparticles, J. Control. Release, 354, 680, 10.1016/j.jconrel.2023.01.047
Qu, 2022, Photothermal scaffolds/surfaces for regulation of cell behaviors, Bioact Mater, 8, 449
Man, 2019, Intracellular photothermal delivery for suspension cells using sharp nanoscale tips in microwells, ACS Nano, 13, 10835, 10.1021/acsnano.9b06025
Raes, 2020, Intracellular delivery of mRNA in adherent and suspension cells by vapor nanobubble photoporation, Nanomicro Lett., 12, 1
Layachi, 2023, Novel opto-fluidic drug delivery system for efficient cellular transfection, J. Nanobiotechnol., 21, 43, 10.1186/s12951-023-01797-3
González-Granado, 2014, Nuclear envelope lamin-a couples actin dynamics with immunological synapse architecture and T Cell activation, Sci. Signal, 7, 1, 10.1126/scisignal.2004872
Walling, 2021, Protean regulation of leukocyte function by nuclear lamins, Trends Immunol., 42, 323, 10.1016/j.it.2021.02.005
Jung, 2021, T cell stiffness is enhanced upon formation of immunological synapse, Elife, 10, 1, 10.7554/eLife.66643
Togo, 2006, Disruption of the plasma membrane stimulates rearrangement of microtubules and lipid traffic toward the wound site, J. Cell Sci., 119, 2780, 10.1242/jcs.03006
Sengupta, 2021, Cholesterol-dependent plasma membrane order (Lo) is critical for antigen-specific clonal expansion of CD4+ T cells, Sci. Rep., 11, 13970, 10.1038/s41598-021-93403-5
Bai, 2017, Acid sphingomyelinase mediates human CD4+ T-cell signaling: potential roles in T-cell responses and diseases, Cell Death Dis., 8, 10.1038/cddis.2017.360
Pinto, 2021, Acid sphingomyelinase deficiency: a clinical and immunological perspective, Int J Mol Sci, 22, 10.3390/ijms222312870
Bai, 2015, Role of acid sphingomyelinase bioactivity in human CD4+ T-cell activation and immune responses, Cell Death Dis, 6, 1, 10.1038/cddis.2015.178
Bhattacharjee, 2018, Cholesterol-dependent cytolysins impair pro-inflammatory macrophage responses, Sci. Rep., 8, 1, 10.1038/s41598-018-24955-2
Miller, 2015, Lipid raft-dependent plasma membrane repair interferes with the activation of B lymphocytes, J. Cell Biol., 211, 1193, 10.1083/jcb.201505030
Houthaeve, 2022, The cellular response to plasma membrane disruption for nanomaterial delivery, Nano Converg., 9
