| Literature DB >> 30607541 |
Wenbo Yang1, Yanxin Han1, Chendie Yang1, Yanjia Chen1, Weilin Zhao1, Xiuxiu Su1, Ke Yang2,3, Wei Jin4.
Abstract
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.Entities:
Keywords: Bcl2-like 11; Cardiac apoptosis; Heart failure; MicroRNA-19b-1; Myocardial infarction
Year: 2019 PMID: 30607541 DOI: 10.1007/s00380-018-01336-3
Source DB: PubMed Journal: Heart Vessels ISSN: 0910-8327 Impact factor: 2.037