首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Synthetic osteogenic growth peptide promotes differentiation of human bone marrow mesenchymal stem cells to osteoblasts via RhoA/ROCK pathway.
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Synthetic osteogenic growth peptide promotes differentiation of human bone marrow mesenchymal stem cells to osteoblasts via RhoA/ROCK pathway.

机译:合成成骨生长肽通过RhoA / ROCK途径促进人骨髓间充质干细胞向成骨细胞分化。

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摘要

The osteogenic growth peptide (OGP) is a naturally occurring tetradecapeptide that has attracted considerable clinical interest as a bone anabolic agent and hematopoietic stimulator. In vitro studies have demonstrated that OGP directly regulates the bone marrow mesenchymal stem cells' (BMSCs) differentiation into osteoblasts. However, the exact mechanism of this process remains unknown. In the present study, we investigated the role of RhoA/ROCK signaling in differentiation along this lineage using human BMSCs. OGP treatment increased the mRNA level of bone morphogenetic protein-2 and alkaline phosphatase activity after osteogenic induction. Analysis of BMSCs induced in the presence of OGP revealed an increase in RhoA activity, and phosphorylation of FAK and cofilin. The ROCK-specific inhibitors, Y27632, blocked the OGP-induced regulation of BMSC differentiation. Taken together, these data suggest that OGP not only acts on BMSCs to stimulate osteogenic differentiation, but also in a dose-dependent manner, and this effect is mediated via the activation of RhoA/ROCK pathway.
机译:成骨生长肽(OGP)是天然存在的四肽,作为骨合成代谢剂和造血刺激剂已引起了广泛的临床兴趣。体外研究表明,OGP直接调节骨髓间充质干细胞(BMSCs)向成骨细胞的分化。但是,此过程的确切机制仍然未知。在本研究中,我们调查了使用人类BMSC沿该谱系分化RhoA / ROCK信号的作用。 OGP处理增加了成骨诱导后骨形态发生蛋白2的mRNA水平和碱性磷酸酶活性。分析在OGP存在下诱导的BMSCs显示RhoA活性增加,FAK和cofilin磷酸化。 ROCK特异性抑制剂Y27632阻断了OGP诱导的BMSC分化调控。综上所述,这些数据表明,OGP不仅作用于BMSC刺激成骨细胞分化,而且还呈剂量依赖性,并且这种作用是通过RhoA / ROCK途径的激活介导的。

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