| Literature DB >> 21186368 |
Jian-Xun Wang1, Jian-Qin Jiao, Qian Li, Bo Long, Kun Wang, Jin-Ping Liu, Yan-Rui Li, Pei-Feng Li.
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.Entities:
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Year: 2010 PMID: 21186368 DOI: 10.1038/nm.2282
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440