Maintenance of Proliferation and Adipogenic Differentiation by Fibroblast Growth Factor-2 and Dexamethasone Through Expression of Hepatocyte Growth Factor in Bone Marrow-derived Mesenchymal Stem Cells
Author(s) -
Ji-Eun Oh,
Young Woo Eom
Publication year - 2016
Publication title -
journal of experimental and biomedical sciences/biomedical science letters
Language(s) - English
Resource type - Journals
eISSN - 2288-7415
pISSN - 1738-3226
DOI - 10.15616/bsl.2016.22.1.1
Subject(s) - hepatocyte growth factor , mesenchymal stem cell , adipogenesis , fibroblast growth factor , endocrinology , medicine , cellular differentiation , ascorbic acid , biology , dexamethasone , growth factor , microbiology and biotechnology , chemistry , biochemistry , receptor , food science , gene
Several studies have investigated the various effects of dexamethasone (Dex) on the proliferation and differentiation of mesenchymal stem cells (MSCs). Previously, we reported that co-treatment with L-ascorbic acid 2-phosphate and fibroblast growth factor (FGF)-2 maintained differentiation potential in MSCs through expression of hepatocyte growth factor (HGF). In this study, we investigated the effects of co-treatment with FGF-2 and Dex on the proliferation and differentiation potential of MSCs during a 2-month culture period. Co-treatment with FGF-2 and Dex increased approximately a 4.7-fold higher accumulation rate of MSC numbers than that by FGF-2 single treatment during a 2-month culture period. Interestingly, co-treatment with FGF-2 and Dex increased expression of HGF and maintained adipogenic differentiation potential during this culture period. These results suggest that co-treatment with FGF-2 and Dex preserves the proliferation and differentiation potential during long-term culture.
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