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首页> 外文期刊>Heart and vessels: An international journal >MicroRNA-19b-1 reverses ischaemia-induced heart failure by inhibiting cardiomyocyte apoptosis and targeting Bcl2 l11/BIM
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MicroRNA-19b-1 reverses ischaemia-induced heart failure by inhibiting cardiomyocyte apoptosis and targeting Bcl2 l11/BIM

机译:MicroRNA-19B-1通过抑制心肌细胞凋亡和靶向BCL2 L11 / BIM来反转缺血性心力衰竭

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摘要

Ischaemia induces cardiac apoptosis and leads to a loss of cardiac function and heart failure after myocardial infarction. MicroRNA-19b-1 (miR-19b-1), a key member of the miR-17/92 cluster, plays crucial roles in inhibiting apoptosis. However, the role of miR-19b-1 in ischaemia-induced heart failure remains unknown. In this study, ischaemia resulted in cardiac apoptosis and the suppression of miR-19b-1 expression, whereas miR-19b-1 overexpression inhibited ischaemia-induced cardiac apoptosis in vivo and in vitro. Moreover, miR-19b-1 not only attenuated the infarct size but also ameliorated heart failure after myocardial infarction, including the changes in the left ventricular ejection fraction and volume load. Mechanically, miR-19-1 targeted and downregulated the mRNA and protein expression of Bcl2l11/BIM, a pro-apoptotic gene of the Bcl-2 family. Together, these results revealed an essential role of miR-19b-1 in ischaemia-induced heart failure.
机译:isChaemia诱导心肌凋亡,导致心肌梗死后心脏功能和心力衰竭丧失。 MicroRNA-19B-1(MIR-19B-1)是miR-17/92簇的关键构件,在抑制细胞凋亡中起着至关重要的作用。 然而,miR-19b-1在iscaemia诱导的心力衰竭中的作用仍然未知。 在这项研究中,患有心肌凋亡和抑制miR-19b-1表达,而miR-19b-1过表达抑制体内和体外体内的患有心肌凋亡。 此外,MIR-19B-1不仅衰减了梗塞大小,而且在心肌梗死后也会改善心力衰竭,包括左心室喷射分数和体积负荷的变化。 机械,miR-19-1靶向和下调BCL2L11 / BIM的mRNA和蛋白表达,BCL-2家族的促凋亡基因。 这些结果在一起揭示了miR-19b-1在iscaemia诱导的心力衰竭中的重要作用。

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