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首页> 外文期刊>The international journal of biochemistry and cell biology >Cyclic biaxial tensile strain promotes bone marrow-derived mesenchymal stem cells to differentiate into cardiomyocyte-like cells by miRNA-27a
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Cyclic biaxial tensile strain promotes bone marrow-derived mesenchymal stem cells to differentiate into cardiomyocyte-like cells by miRNA-27a

机译:循环双轴拉伸菌株促进骨髓衍生的间充质干细胞通过miRNA-27a分化成心肌细胞样细胞

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摘要

A physical stimuli, it has been reported that cyclic tensile strain can promote bone marrow-derived mesenchymal stem cells (BMSCs) to differentiate into cardiomyocytes, but the underlying mechanisms have been poorly elucidated so far. Here, we used a mimicking loading strain, cyclic biaxial tensile strain (CBTS), and found it can promote BMSCs to differentiate into cardiomyocytes. When the CBTS were loaded, the cells expressed cardiac-specific markers GATA4, TNNT2, MEF-2c, and Cx43, meanwhile we found miR-27a decreased and stem cell factor (SCF) increased. When we overexpressed miR-27a, the cardiac-specific markers were down-regulated; we got the same results when SCF was knocked down by siRNA. Interestingly, we found SCF is a potential target of miR-27a by a bioinformatic analysis. So, we overexpressed miR-27a, and found SCF decreased both in mRNA and protein level. And, When miR-27a was co-transfected with SCF-3'UTR, it significantly reduced the luciferase activity, but not when co-transfected with SCF-3'UTR mutation plasmid. Furthermore, after transfected both miR-27a and SCF siRNA, and the protein expression of the markers were more down-regulated than that of single of them. Taken together, we found CBTS can promote BMSCs to differentiate into cardiomyocytes, and miR-27a functions as a mechano-sensitive miRNA in this process by targeting SCF.
机译:据报道,物理刺激,据报道,循环拉伸菌株可以促进骨髓衍生的间充质干细胞(BMSC)分化成心肌细胞,但到目前为止,下面的潜在机制却很难阐明。在这里,我们使用模仿负载应变,循环双轴拉伸菌株(CBT),发现它可以促进BMSCs分化成心肌细胞。当加载CBT时,细胞表达心脏特异性标记GATA4,TNNT2,MEF-2C和CX43,同时我们发现MIR-27A降低,干细胞因子(SCF)增加。当我们过表达miR-27a时,心脏特异性标记被下调;当SCF被siRNA击倒时,我们得到了相同的结果。有趣的是,通过生物信息分析,我们发现SCF是miR-27a的潜在目标。因此,我们过表达的miR-27a,发现SCF在mRNA和蛋白质水平中降低。并且,当用SCF-3'UTR共转染miR-27a时,它显着降低了荧光素酶活性,但不能与SCF-3'UTR突变质粒共转染时。此外,在转染miR-27a和scf siRNA之后,并且标记物的蛋白质表达比单个单一的蛋白质表达更下调。一起携带,我们发现CBT可以促进BMSCs分化成心肌细胞,并且MiR-27a通过靶向SCF在该过程中作为机械敏感的miRNA。

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