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Nuclear miR-665 aggravates heart failure via suppressing phosphatase and tensin homolog transcription

查看全文 作  者:Jiahui [1,2]Fan;Xudong [1,2]Zhang;Xiang [1,2]Nie;Huaping [1,2]Li;Shuai [1,2]Yuan;Beibei [1,2]Dai;Jiabing [1,2]Zhan;Zheng [1,2]Wen;Jiangang [1,2]Jiang;Chen [1,2]Chen;Daowen [1,2]Wang 高影响力作者 机构地区:[1]Division of Cardiology,Department of Internal Medicine,Tongji Hospital,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430030,China;[2]Hubei Key Laboratory of Genetics and Molecular Mechanisms of Cardiological Disorders,Wuhan 430030,China高影响力机构 出  处:《Science China(Life Sciences)》索引2020年第63卷第5期,共13页高影响力期刊 基  金:supported by grant from the National Natural Science Foundation of China(81822002,81630010,81790624,91839302,31771264 and 31800973)。 摘  要:Although numerous miRNAs have been discovered,their functions in the different subcellular organelles have remained obscure.In this study,we found that miR-665 was enriched in the nucleus of cardiomyocytes,and then investigated the underlying role of nuclear miR-665 in heart failure.RNA fluorescence in situ hybridization assays in human heart tissue sections and primary cardiomyocytes showed that miR-665 was localized in the nucleus of cardiomyocytes.Increased expression of nuclear miR-665 was observed not only in the cardiomyocytes isolated from the heart of mice treated in vivo by transverse aortic constriction(TAC),but also in phenylephrine(PE)-treated cultured cardiomyocytes in vitro.To further explore the role of miR-665 in heart failure,a type 9 recombinant adeno-associated virus(rAAV)system was employed to manipulate the expression of miR-665 in mice.Overexpression of miR-665 aggravated TAC-induced cardiac dysfunction,while down-expression of miR-665 showed opposite effects.Bioinformatic prediction and biological validation confirmed that the PTEN(phosphatase and tensin homolog)gene was one of the targets of miR-665 in the nucleus.Furthermore,restoring PTEN expression significantly eliminated the destructive effects of miR-665 over-expression in TAC-induced cardiac dysfunction.Our data showed that nuclear miR-665 aggravates heart failure via inhibiting PTEN expression,which provided a therapeutic approach for heart failure. 关 键 词:nucleus miR-665 heart failure phosphatase and tensin homolog
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