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首页> 外文期刊>Cell death & disease. >Knockdown of SIRT7 enhances the osteogenic differentiation of human bone marrow mesenchymal stem cells partly via activation of the Wnt/β-catenin signaling pathway
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Knockdown of SIRT7 enhances the osteogenic differentiation of human bone marrow mesenchymal stem cells partly via activation of the Wnt/β-catenin signaling pathway

机译:敲低SIRT7可以部分地通过激活Wnt / β -catenin信号通路来增强人骨髓间充质干细胞的成骨分化

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摘要

Sirtuin 7 (SIRT7) is a NAD+-dependent deacetylase in the sirtuin family. In a previous study, human bone marrow mesenchymal stem cells (hBMSCs) with reduced SIRT7 activity were developed to evaluate the effect of SIRT7 on osteogenesis. SIRT7 knockdown significantly enhanced osteoblast-specific gene expression, alkaline phosphatase activity, and mineral deposition in vitro . Additionally, SIRT7 knockdown upregulated β -catenin. The enhanced osteogenesis due to SIRT7 knockdown was partially rescued by a Wnt/ β -catenin inhibitor. Furthermore, SIRT7 knockdown hBMSCs combined with a chitosan scaffold significantly promoted bone formation in a rat tibial defect model, as determined by imaging and histological examinations. These findings suggest that SIRT7 has an essential role in osteogenic differentiation of hBMSCs, partly by activation of the Wnt/ β -catenin signaling pathway.
机译:Sirtuin 7(SIRT7)是Sirtuin家族中NAD + 依赖性脱乙酰基酶。在先前的研究中,开发了具有降低的SIRT7活性的人骨髓间充质干细胞(hBMSC),以评估SIRT7对成骨的作用。 SIRT7敲低显着增强了成骨细胞特异性基因表达,碱性磷酸酶活性和体外矿物质沉积。此外,SIRT7敲低上调了β-连环蛋白。 Wnt /β-catenin抑制剂可部分挽救由于SIRT7敲低引起的成骨作用增强。此外,通过成像和组织学检查确定,SIRT7组合式hBMSC与壳聚糖支架相结合可显着促进大鼠胫骨缺损模型中的骨形成。这些发现表明SIRT7在hBMSC的成骨分化中具有重要作用,部分是通过激活Wnt /β-catenin信号传导途径。

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