首页> 外文期刊>International journal of molecular medicine >Silencing of angiotensin-converting enzyme by RNA interference prevents H9c2 cardiomyocytes from apoptosis induced by anoxia/reoxygenation through regulation of the intracellular renin-angiotensin system
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Silencing of angiotensin-converting enzyme by RNA interference prevents H9c2 cardiomyocytes from apoptosis induced by anoxia/reoxygenation through regulation of the intracellular renin-angiotensin system

机译:RNA干扰使血管紧张素转换酶沉默,通过调节细胞内肾素-血管紧张素系统,防止H9c2心肌细胞缺氧/复氧诱导的凋亡

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摘要

Inhibition of the angiotensin-converting enzyme (ACE) attenuated apoptotic cardiomyocytes induced by ischemic reperfusion (I/R). However, it is difficult to evaluate the effects of inhibition of the intracellular ACE in vivo. The objective of this study was to determine whether the apoptosis in H9c2 cardiomyocytes following anoxia/reoxygenation (A/R) would be improved by the silencing of intracellular ACE by RNA interference (RNAi). H9c2 cardiomyocytes were subjected to A/R 48 h following transfection with ACE-shRNA plasmid. The results showed that the gene silencing of intracellular ACE significantly inhibited the decrease of cell viability and the increase of apoptotic H9c2 cardiomyocytes undergoing A/R. Additionally, the gene silencing of intracellular ACE significantly promoted the expression of ACE2, decreased caspase-3 activity and Bax levels, and enhanced the expression of Bcl-2 in H9c2 cardiomyocytes subjected to A/R. The results suggest that the gene silencing of intracellular ACE holds great potential in the treatment of cardiomyocyte apoptosis following I/R injury through the regulation of the intracellular renin-angiotensin system, thereby regulating the intrinsic pathway of apoptosis.
机译:缺血再灌注(I / R)诱导的血管紧张素转换酶(ACE)的抑制减弱了凋亡的心肌细胞。但是,难以评估体内抑制细胞内ACE的效果。这项研究的目的是确定是否可以通过RNA干扰(RNAi)沉默细胞内ACE来改善缺氧/复氧(A / R)后H9c2心肌细胞的凋亡。用ACE-shRNA质粒转染H9c2心肌细胞48 h。结果表明,细胞内ACE基因的沉默显着抑制了A / R过程中细胞活力的下降和凋亡的H9c2心肌细胞的增加。另外,细胞内ACE的基因沉默显着促进了接受A / R的H9c2心肌细胞中ACE2的表达,降低了caspase-3活性和Bax水平,并增强了Bcl-2的表达。结果表明,通过调节细胞内肾素-血管紧张素系统,从而调节细胞凋亡的内在途径,细胞内ACE的基因沉默在治疗I / R损伤后的心肌细胞凋亡中具有巨大潜力。

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