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U0126 promotes osteogenesis of rat bone-marrow-derived mesenchymal stem cells by activating BMP/Smad signaling pathway

机译:U0126通过激活BMP / Smad信号通路促进大鼠骨髓间充质干细胞的成骨

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摘要

U0126 has been reported as a specific inhibitor of the ERK1/2 signaling pathway, which plays a vital role during the osteogenic differentiation of mesenchymal stem cells (MSCs). We report the positive effect of U0126 on the osteogenesis of rat MSCs. We find that U0126 promotes the osteogenic differentiation of rat MSCs as demonstrated by the quantitative real-time polymerase chain reaction for osteogenic markers, alkaline phosphatase activity and calcium nodule formation. Our data indicate that U0126 enhances the BMP/Smad signaling pathway in rat MSCs, while inhibiting the ERK1/2 signaling pathway. Furthermore, Western blot results demonstrate that U0126 increases Smad1/5/8 phosphorylation synergistically with beta-glycerophosphate. In addition, U0126 significantly increases the expression of BMP2 during the process of osteogenesis in rat MSCs and the level of phosphorylated Smad1/5/8 is significantly reduced by BMP2 antibody, suggesting that U0126 also promotes the expression of BMP2 to enhance Smad proteins phosphorylation. Thus, we demonstrate a novel function for U0126 in promoting osteogenic differentiation of rat MSCs by the activation of the BMP/Smad signaling pathway.
机译:据报道,U0126是ERK1 / 2信号通路的特异性抑制剂,在间充质干细胞(MSCs)的成骨分化中起着至关重要的作用。我们报道了U0126对大鼠MSCs成骨的积极作用。我们发现,U0126促进大鼠MSC的成骨分化,如成骨标记,碱性磷酸酶活性和钙结节形成的定量实时聚合酶链反应所证明。我们的数据表明,U0126增强了大鼠MSC中的BMP / Smad信号传导途径,同时抑制了ERK1 / 2信号传导途径。此外,蛋白质印迹结果表明,U0126与β-甘油磷酸酯协同增加Smad1 / 5/8磷酸化。此外,U0126在成骨过程中显着增加大鼠MSC中BMP2的表达,并且BMP2抗体显着降低了磷酸化Smad1 / 5/8的水平,这表明U0126还促进BMP2的表达以增强Smad蛋白的磷酸化。因此,我们证明了U0126通过激活BMP / Smad信号通路促进大鼠MSC的成骨分化的新功能。

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