Activin A expression regulates multipotency of mesenchymal progenitor cells.

Abstract : ABSTRACT : INTRODUCTION : Bone marrow (BM) stroma currently represents the most common and investigated source of mesenchymal progenitor cells (MPCs); however, comparable adult progenitor or stem cells have also been isolated from a wide variety of tissues. This study aims to assess the functional similarities of MPCs from different tissues and to identify specific factor(s) related to their multipotency. METHODS : For this purpose, we directly compared MPCs isolated from different adult tissues, including bone marrow, tonsil, muscle, and dental pulp. We first examined and compared proliferation rates, immunomodulatory properties, and multidifferentiation potential of these MPCs in vitro. Next, we specifically evaluated activin A expression profile and activin A:follistatin ratio in MPCs from the four sources. RESULTS : The multidifferentiation potential of the MPCs is correlated with activin A level and/or the activin A:follistatin ratio. Interestingly, by siRNA-mediated activin A knockdown, activin A was shown to be required for the chondrogenic and osteogenic differentiation of MPCs. These findings strongly suggest that activin A has a pivotal differentiation-related role in the early stages of chondrogenesis and osteogenesis while inhibiting adipogenesis of MPCs. CONCLUSIONS : This comparative analysis of MPCs from different tissue sources also identifies bone marrow-derived MPCs as the most potent MPCs in terms of multilineage differentiation and immunosuppression, two key requirements in cell-based regenerative medicine. In addition, this study implicates the significance of activin A as a functional marker of MPC identity.
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Stem Cell Research and Therapy, BioMed Central, 2010, 1 (2), pp.11. 〈10.1186/scrt11〉
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Farida Djouad, Wesley Jackson, Brent Bobick, Sasa Janjanin, Yingjie Song, et al.. Activin A expression regulates multipotency of mesenchymal progenitor cells.. Stem Cell Research and Therapy, BioMed Central, 2010, 1 (2), pp.11. 〈10.1186/scrt11〉. 〈inserm-00622572〉

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