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Downregulation of miRNA-1-3p modulates cyclic stretch-mediated proliferation of vascular smooth muscle cells through regulation of ETS-1

机译:MiRNA-1-3P的下调通过ETS-1调节调节血管平滑肌细胞的循环拉伸介导的增殖

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Mechanical stretch modulates the proliferation of vascular smooth muscle cells (VSMCs) and plays an important role in the pathogenesis of hypertension, but the underlying mechanisms are unclear. We investigated the role of microRNA- 1-3p (miRNA-1-3p) on the proliferation of VSMCs induced by mechanical cyclic stretch. Our data show that miRNA-1-3p is downregulated in the aorta of the spontaneous hypertension rat (SHR). Pathological mechanical stretch at 15% suppressed the expression of miRNA-1-3p, calponin and SM22, but enhanced the proliferation of VSMCs as well as the expression of the V-ets erythroblastosis virus E26 oncogene homolog 1 (ETS-1), collagen type I alpha (Col-1a), collagen type III alpha (Col-3a) and elastin. Overexpression of miRNA-1-3p inhibited cell proliferation and induced the expression of calponin and SM22, but decreased the expression of ETS-1, Col-1a, Col-3a and elastin. Mechanical stretch at 15% combined with losartan treatment increased the expression of miRNA-1-3p, calponin and SM22, and decreased the expression of ETS-1, Col-1a and Col-3a. Dual luciferase reporter assays revealed ETS-1 as a direct target of miRNA-1-3p. These findings suggest that miRNA-1-3p regulates VSMC function through ETS-1 regulation during hypertension-induced vascular remodeling. MiRNA-1-3p may be a viable therapeutic target for hypertension.
机译:机械拉伸调节血管平滑肌细胞(VSMC)的增殖和起着高血压的发病中起重要作用,但潜在的机制还不清楚。我们对机械循环拉伸引起的血管平滑肌细胞增殖研究微小RNA-1-3 P(miRNA的-1-3 P)的作用。我们的数据显示了miRNA-1-3 P在自发性高血压大鼠(SHR)的主动脉下调。在15%的病理机械拉伸抑制的miRNA-1-3 P,钙调蛋白和SM22的表达,但增强的血管平滑肌细胞的增殖,以及在V-ETS成红细胞增多症病毒E26的癌基因同源物1(ETS-1),胶原蛋白型表达我α(的Col-1a)中,胶原III型α(的Col-3a)和弹性蛋白。的miRNA-1-3 P抑制细胞增殖的过表达,并诱导钙调蛋白和SM22的表达,但降低了ETS-1,的Col-1A,的Col-3a和弹性蛋白的表达。在15%与氯沙坦治疗组合的机械拉伸增加的miRNA-1-3 P,钙调蛋白和SM22的表达,和降低的ETS-1,的Col-1A和Col-3a的表达。双荧光素酶报告测定揭示ETS-1作为的miRNA-1-3 P的直接靶。这些结果表明,miRNA的-1-3 P高血压引起血管重建过程中调节VSMC功能通过ETS-1调控。的miRNA 1-3 P可以是用于高血压的可行的治疗靶标。

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