首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Expression of Sp7 in Satb2-induced osteogenic differentiation of mouse bone marrow stromal cells is regulated by microRNA-27a
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Expression of Sp7 in Satb2-induced osteogenic differentiation of mouse bone marrow stromal cells is regulated by microRNA-27a

机译:Sp7在Satb2诱导的小鼠骨髓基质细胞成骨分化中的表达受microRNA-27a调控

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摘要

Satb2 is a special AT-rich binding transcription factor essential for osteoblast differentiation and bone formation. Specific microRNAs (miRNAs) have been identified to regulate the complex process of osteogenic differentiation. It remains unclear how miRNA expressions is changed in the Satb2-induced osteogenic differentiation of bone marrow stromal cells (BMSCs). From the miRNA expression profile data collected by us from Satb2-induced osteogenic differentiation of mouse BMSCs, we found that miR-27a was significantly down-regulated relative to non-treated cells 7 days post induction. By in silico analysis, we identified Sp7 as a miR-27a targeting gene and verified the findings by Western blot analysis, qRT-PCR, and luciferase reporter assays. We also analyzed the function of miR-27a in osteogenic differentiation by transfection of exogenous miR-27a into BMSCs. Overexpression of miR-27a remarkably inhibited the expression of Sp7 and attenuated Satb2-induced osteogenic differentiation. Our results suggest that expression of Sp7 during the early stage of Satb2-induced osteogenic differentiation of BMSCs is regulated by miR-27a.
机译:Satb2是一种特殊的富含AT的结合转录因子,对于成骨细胞的分化和骨骼形成至关重要。已经确定了特定的microRNA(miRNA)来调节成骨分化的复杂过程。尚不清楚在Satb2诱导的骨髓基质细胞(BMSCs)的成骨分化中,miRNA的表达如何变化。从我们从Satb2诱导的小鼠骨髓间充质干细胞的成骨分化中收集的miRNA表达谱数据中,我们发现相对于未处理的细胞,诱导后7天,miR-27a显着下调。通过计算机分析,我们将Sp7鉴定为miR-27a靶向基因,并通过Western印迹分析,qRT-PCR和荧​​光素酶报告基因分析验证了该发现。我们还通过将外源性miR-27a转染到BMSC中来分析miR-27a在成骨分化中的功能。 miR-27a的过表达显着抑制Sp7的表达,并减弱Satb2诱导的成骨分化。我们的结果表明,Satb2诱导的BMSCs成骨分化早期Sp7的表达受miR-27a调控。

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