Effects of Medium Supplements on Proliferation, Differentiation Potential, and In Vitro Expansion of Mesenchymal Stem Cells

Stem cells translational medicine - Tập 1 Số 11 - Trang 771-782 - 2012
Borzo Gharibi1, Francis J. Hughes1
1Department of Periodontology, Dental Institute, Guy's Hospital, King's College London, London, United Kingdom

Tóm tắt

Abstract

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/adipocytic 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.

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Tài liệu tham khảo

Pittenger, 1999, Multilineage potential of adult human mesenchymal stem cells, Science, 284, 143, 10.1126/science.284.5411.143

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/pnas.132252399

Quarto, 2001, Repair of large bone defects with the use of autologous bone marrow stromal cells, N Engl J Med, 344, 385, 10.1056/NEJM200102013440516

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

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/j.joms.2009.08.031

Mesimäki, 2009, Novel maxillary reconstruction with ectopic bone formation by GMP adipose stem cells, Int J Oral Maxillofac Surg, 38, 201, 10.1016/j.ijom.2009.01.001

Le Blanc, 2008, Mesenchymal stem cells for treatment of steroid-resistant, severe, acute graft-versus-host disease: A phase II study, Lancet, 371, 1579, 10.1016/S0140-6736(08)60690-X

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

Timmers, 2011, Human mesenchymal stem cell-conditioned medium improves cardiac function following myocardial infarction, Stem Cell Res, 6, 206, 10.1016/j.scr.2011.01.001

Amado, 2005, Cardiac repair with intramyocardial injection of allogeneic mesenchymal stem cells after myocardial infarction, Proc Natl Acad Sci USA, 102, 11474, 10.1073/pnas.0504388102

Kharaziha, 2009, Improvement of liver function in liver cirrhosis patients after autologous mesenchymal stem cell injection: A phase I-II clinical trial, Eur J Gastroenterol Hepatol, 21, 1199, 10.1097/MEG.0b013e32832a1f6c

Tfilin, 2010, Mesenchymal stem cells increase hippocampal neurogenesis and counteract depressive-like behavior, Mol Psychiatry, 15, 1164, 10.1038/mp.2009.110

Dwyer, 2010, Advances in mesenchymal stem cell-mediated gene therapy for cancer, Stem Cell Res Ther, 1, 25, 10.1186/scrt25

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/jcp.20911

Sotiropoulou, 2006, Characterization of the optimal culture conditions for clinical scale production of human mesenchymal stem cells, Stem Cells, 24, 462, 10.1634/stemcells.2004-0331

Both, 2007, A rapid and efficient method for expansion of human mesenchymal stem cells, Tissue Eng, 13, 3, 10.1089/ten.2005.0513

Tsutsumi, 2001, Retention of multilineage differentiation potential of mesenchymal cells during proliferation in response to FGF, Biochem Biophys Res Commun, 288, 413, 10.1006/bbrc.2001.5777

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/jcp.20238

Martin, 1997, Fibroblast growth factor-2 supports ex vivo expansion and maintenance of osteogenic precursors from human bone marrow, Endocrinology, 138, 4456, 10.1210/endo.138.10.5425

Bianchi, 2003, Ex vivo enrichment of mesenchymal cell progenitors by fibroblast growth factor 2, Exp Cell Res, 287, 98, 10.1016/S0014-4827(03)00138-1

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/stemcells.2005-0176

Pricola, 2009, Interleukin-6 maintains bone marrow-derived mesenchymal stem cell stemness by an ERK1/2-dependent mechanism, J Cell Biochem, 108, 577, 10.1002/jcb.22289

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/ten.tea.2009.0230

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/jbmr.424

Neubauer, 2004, Basic fibroblast growth factor enhances PPARgamma ligand-induced adipogenesis of mesenchymal stem cells, FEBS Lett, 577, 277, 10.1016/j.febslet.2004.10.020

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/s10616-007-9092-1

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/stem.661

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/jcb.23097

Hayflick, 1961, The serial cultivation of human diploid cell strains, Exp Cell Res, 25, 585, 10.1016/0014-4827(61)90192-6

Bonab, 2006, Aging of mesenchymal stem cell in vitro, BMC Cell Biol, 7, 14, 10.1186/1471-2121-7-14

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/j.1582-4934.2009.00931.x

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/scd.2008.0324

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/s11033-010-0665-2

Chamberlain, 2007, Concise review: Mesenchymal stem cells: Their phenotype, differentiation capacity, immunological features, and potential for homing, Stem Cells, 25, 2739, 10.1634/stemcells.2007-0197

Dominici, 2006, Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement, Cytotherapy, 8, 315, 10.1080/14653240600855905

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

Sacchetti, 2007, Self-renewing osteoprogenitors in bone marrow sinusoids can organize a hematopoietic microenvironment, Cell, 131, 324, 10.1016/j.cell.2007.08.025