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miR-499 通过靶向钙调神经磷酸酶和动力相关蛋白 1 调节线粒体动力学。

miR-499 regulates mitochondrial dynamics by targeting calcineurin and dynamin-related protein-1.

机构信息

Division of Cardiovascular Research, National Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.

出版信息

Nat Med. 2011 Jan;17(1):71-8. doi: 10.1038/nm.2282. Epub 2010 Dec 26.

Abstract

Myocardial infarction is a leading cause of mortality worldwide. Here we report that modulation of microRNA-499 (miR-499) levels affects apoptosis and the severity of myocardial infarction and cardiac dysfunction induced by ischemia-reperfusion. We found that both the α- and β-isoforms of the calcineurin catalytic subunit are direct targets of miR-499 and that miR-499 inhibits cardiomyocyte apoptosis through its suppression of calcineurin-mediated dephosphorylation of dynamin-related protein-1 (Drp1), thereby decreasing Drp1 accumulation in mitochondria and Drp1-mediated activation of the mitochondrial fission program. We also found that p53 transcriptionally downregulates miR-499 expression. Our data reveal a role for miR-499 in regulating the mitochondrial fission machinery and we suggest that modulation of miR-499 levels may provide a therapeutic approach for treating myocardial infarction.

摘要

心肌梗死是全球范围内导致死亡的主要原因之一。在这里,我们报告说,miR-499(微小 RNA-499)水平的调节会影响细胞凋亡以及缺血再灌注引起的心肌梗死和心功能障碍的严重程度。我们发现钙调神经磷酸酶催化亚基的α和β两种异构体都是 miR-499 的直接靶标,miR-499 通过抑制钙调神经磷酸酶介导的动力相关蛋白 1(Drp1)去磷酸化来抑制心肌细胞凋亡,从而减少线粒体中 Drp1 的积累和 Drp1 介导的线粒体分裂程序的激活。我们还发现 p53 转录下调 miR-499 的表达。我们的数据揭示了 miR-499 在调节线粒体分裂机制中的作用,并表明调节 miR-499 水平可能为治疗心肌梗死提供一种治疗方法。

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