[HTML][HTML] Circular RNA mediates cardiomyocyte death via miRNA-dependent upregulation of MTP18 expression

K Wang, TY Gan, N Li, CY Liu, LY Zhou… - Cell Death & …, 2017 - nature.com
K Wang, TY Gan, N Li, CY Liu, LY Zhou, JN Gao, C Chen, KW Yan, M Ponnusamy…
Cell Death & Differentiation, 2017nature.com
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 …
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.
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