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首页> 外文期刊>Cell death & disease. >Knockdown of FOXA2 enhances the osteogenic differentiation of bone marrow-derived mesenchymal stem cells partly via activation of the ERK signalling pathway
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Knockdown of FOXA2 enhances the osteogenic differentiation of bone marrow-derived mesenchymal stem cells partly via activation of the ERK signalling pathway

机译:抑制FOXA2可以部分激活ERK信号通路,从而增强骨髓源性间充质干细胞的成骨分化

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Forkhead box protein A2 (FOXA2) is a core transcription factor that controls cell differentiation and may have an important role in bone metabolism. However, the role of FOXA2 during osteogenic differentiation of bone marrow-derived mesenchymal stem cells (BMSCs) remains largely unknown. In this study, decreased expression of FOXA2 was observed during osteogenic differentiation of rat BMSCs (rBMSCs). FOXA2 knockdown significantly increased osteoblast-specific gene expression, the number of mineral deposits and alkaline phosphatase activity, whereas FOXA2 overexpression inhibited osteogenesis-specific activities. Moreover, extracellular signal-regulated protein kinase (ERK) signalling was upregulated following knockdown of FOXA2. The enhanced osteogenesis due to FOXA2 knockdown was partially rescued by an ERK inhibitor. Using a rat tibial defect model, a rBMSC sheet containing knocked down FOXA2 significantly improved bone healing. Collectively, these findings indicated that FOXA2 had an essential role in osteogenic differentiation of BMSCs, partly by activation of the ERK signalling pathway.
机译:前叉箱蛋白A2(FOXA2)是控制细胞分化的核心转录因子,可能在骨代谢中起重要作用。但是,FOXA2在骨髓来源的间充质干细胞(BMSCs)的成骨分化中的作用仍然未知。在这项研究中,在大鼠BMSC(rBMSC)的成骨分化过程中观察到FOXA2的表达降低。 FOXA2敲低显着增加成骨细胞特异性基因表达,矿物质沉积的数量和碱性磷酸酶活性,而FOXA2过表达抑制成骨细胞特异性活性。而且,敲低FOXA2后,细胞外信号调节蛋白激酶(ERK)信号被上调。由于FOXA2敲低而增强的成骨作用可通过ERK抑制剂部分挽救。使用大鼠胫骨缺损模型,包含被敲低的FOXA2的rBMSC床单显着改善了骨愈合。总体而言,这些发现表明FOXA2在BMSC的成骨分化中起着重要作用,部分是通过激活ERK信号通路来实现的。

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