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      Biphasic effects of TGFβ1 on BMP9-induced osteogenic differentiation of mesenchymal stem cells.

      BMB reports
      Animals, Cell Differentiation, Cell Line, Collagen Type I, genetics, metabolism, G0 Phase, G1 Phase, Growth Differentiation Factor 2, pharmacology, HCT116 Cells, HEK293 Cells, Humans, Mesenchymal Stromal Cells, cytology, Mice, Osteocalcin, Osteogenesis, Osteopontin, Recombinant Proteins, Smad Proteins, Transforming Growth Factor beta1

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          Abstract

          We have found that the previously uncharacterized bone morphogenetic protein-9 (BMP9) is one of the most osteogenic factors. However, it is unclear if BMP9 cross-talks with TGFβ1 during osteogenic differentiation. Using the recombinant BMP9 adenovirus, we find that low concentration of rhTGFβ1 synergistically induces alkaline phosphatase activity in BMP9-transduced C3H10T1/2 cells and produces more pronounced matrix mineralization. However, higher concentrations of TGFβ1 inhibit BMP9-induced osteogenic activity. Real-time PCR and Western blotting indicate that BMP9 in combination with low dose of TGFβ1 potentiates the expression of later osteogenic markers osteopontin, osteocalcin and collagen type 1 (COL1a2), while higher concentrations of TGFβ1 decrease the expression of osteopontin and osteocalcin but not COL1a2. Cell cycle analysis reveals that TGFβ1 inhibits C3H10T1/2 proliferation in BMP9-induced osteogenesis and restricts the cells in G(0)/G(1) phase. Our findings strongly suggest that TGFβ1 may exert a biphasic effect on BMP9-induced osteogenic differentiation of mesenchymal stem cells.

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