4.7 Article

Platelet-Derived Growth Factor BB Enhances Osteogenesis of Adipose-Derived But Not Bone Marrow-Derived Mesenchymal Stromal/Stem Cells

期刊

STEM CELLS
卷 33, 期 9, 页码 2773-2784

出版社

WILEY-BLACKWELL
DOI: 10.1002/stem.2060

关键词

Tissue engineering; Platelet-derived growth factor; Bone; Stem cells

资金

  1. Johns Hopkins University Center for Musculoskeletal Research
  2. American Society for Bone and Moneral Research [2013CEA13]
  3. NSF CAREER award [1350554]
  4. Maryland Stem Cell Research Fund [2014-MSCRFI-0699]
  5. E. Virginia and David Baldwin Research Fund
  6. NIH [1R01EB016721]
  7. NIH Ruth L Kirschtein National Research Service Award
  8. NIH Cancer Nanotechnology Training Center at the JHU Institute for Nanobiotechnology [R25CA153952]
  9. National Science Foundation
  10. Directorate For Engineering
  11. Div Of Chem, Bioeng, Env, & Transp Sys [1350554] Funding Source: National Science Foundation

向作者/读者索取更多资源

Tissue engineering using mesenchymal stem cells (MSCs) holds great promise for regenerating critically sized bone defects. While the bone marrow-derived MSC is the most widely studied stromal/stem cell type for this application, its rarity within bone marrow and painful isolation procedure have motivated investigation of alternative cell sources. Adipose-derived stromal/stem cells (ASCs) are more abundant and more easily procured; furthermore, they also possess robust osteogenic potency. While these two cell types are widely considered very similar, there is a growing appreciation of possible innate differences in their biology and response to growth factors. In particular, reports indicate that their osteogenic response to platelet-derived growth factor BB (PDGF-BB) is markedly different: MSCs responded negatively or not at all to PDGF-BB while ASCs exhibited enhanced mineralization in response to physiological concentrations of PDGF-BB. In this study, we directly tested whether a fundamental difference existed between the osteogenic responses of MSCs and ASCs to PDGF-BB. MSCs and ASCs cultured under identical osteogenic conditions responded disparately to 20 ng/ml of PDGF-BB: MSCs exhibited no difference in mineralization while ASCs produced more calcium per cell. siRNA-mediated knockdown of PDGFRb within ASCs abolished their ability to respond to PDGF-BB. Gene expression was also different; MSCs generally downregulated and ASCs generally upregulated osteogenic genes in response to PDGF-BB. ASCs transduced to produce PDGF-BB resulted in more regenerated bone within a critically sized murine calvarial defect compared to control ASCs, indicating PDGF-BB used specifically in conjunction with ASCs might enhance tissue engineering approaches for bone regeneration.

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