| Literature DB >> 28498369 |
Kun Wang1, Tian-Yi Gan2, Na Li3, Cui-Yun Liu1, Lu-Yu Zhou1, Jin-Ning Gao1, Chao Chen1, Kao-Wen Yan1, Murugavel Ponnusamy1, Yu-Hui Zhang2, Pei-Feng Li1.
Abstract
Circular RNAs (circRNAs) have important roles in several cellular processes. No study has established the pathophysiological role for circRNAs in the heart. Here, we show that a circRNA (mitochondrial fission and apoptosis-related circRNA (MFACR)) regulates mitochondrial fission and apoptosis in the heart by directly targeting and downregulating miR-652-3p; this in turn blocks mitochondrial fission and cardiomyocyte cell death by suppressing MTP18 translation. MTP18 deficiency reduces mitochondrial fission and suppresses cardiomyocyte apoptosis and MI. miR-652-3p directly downregulates MTP18 and attenuates mitochondrial fission, cardiomyocyte apoptosis, and MI in vitro and in vivo. MFACR directly sequesters miR-652-3p in the cytoplasm and inhibits its activity. MFACR knockdown in cardiomyocytes and mice attenuates mitochondrial fission and MI. Our results reveal a crucial role for circRNA in regulating mitochondrial dynamics and apoptosis in the heart; as such, circRNAs may serve as a potential therapeutic avenue for cardiovascular diseases.Entities:
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Year: 2017 PMID: 28498369 PMCID: PMC5442477 DOI: 10.1038/cdd.2017.61
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828