Institute for Cardiovascular Regeneration, Center of Molecular Medicine, Goethe University, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.
Nat Rev Cardiol. 2015 Mar;12(3):135-42. doi: 10.1038/nrcardio.2014.207. Epub 2014 Dec 16.
MicroRNAs (miRNAs) are small noncoding RNAs that block translation or induce degradation of mRNA and thereby control patterns of gene expression. Acute myocardial infarction is a common cardiovascular event that results in cardiac remodelling and can consequently lead to the development of chronic heart failure. Several miRNAs have been shown to control important processes that contribute to the pathophysiological consequences of acute myocardial infarction. miRNAs can either promote or inhibit cardiomyocyte cell death, and also regulate postischaemic neovascularization. Cardiac regeneration can also be regulated by miRNAs that control cardiomyocyte proliferation or interfere with cardioprotective effects mediated by stem or progenitor cells. miRNAs can also be used for direct reprogramming of cardiac fibroblasts into cardiomyocytes. In this Review, we focus on the current understanding of the role of miRNAs in these processes, and particularly discuss the therapeutic potential of miRNAs in treating acute myocardial infarction.
微小 RNA(miRNA)是一类小的非编码 RNA,可以阻断 mRNA 的翻译或诱导其降解,从而控制基因表达模式。急性心肌梗死是一种常见的心血管事件,可导致心肌重构,并可能导致慢性心力衰竭的发生。已有研究表明,多种 miRNA 可控制对急性心肌梗死病理生理后果有重要作用的过程。miRNA 可以促进或抑制心肌细胞死亡,并调节缺血后新生血管生成。miRNA 还可以通过控制心肌细胞增殖或干扰干细胞或祖细胞介导的心脏保护作用来调节心脏再生。miRNA 也可用于将心脏成纤维细胞直接重编程为心肌细胞。在本综述中,我们重点关注 miRNA 在这些过程中的作用的最新认识,并特别讨论了 miRNA 在治疗急性心肌梗死方面的治疗潜力。