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靶向 microRNA-490-3p-ATG4B-自噬轴缓解缺血再灌注引起的心肌损伤。

Targeting the MicroRNA-490-3p-ATG4B-Autophagy Axis Relieves Myocardial Injury in Ischemia Reperfusion.

机构信息

Department of Cardiology, Liuzhou Traditional Chinese Medical Hospita, The Third Affiliated Hospital of Guangxi University of Chinese Medicine, Liuzhou, 545001, People's Republic of China.

Department of Cardiology, Nanjing Lishui People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, No. 86, Chongwen Road, Lishui District, Nanjing, 211200, Jiangsu, People's Republic of China.

出版信息

J Cardiovasc Transl Res. 2021 Feb;14(1):173-183. doi: 10.1007/s12265-020-09972-9. Epub 2020 May 31.

Abstract

We investigated the potential role of miR-490-3p in ischemia reperfusion (IR) injury. We first determined the expression of miR-490-3p and autophagy-related 4B cysteine (ATG4B) in IR. Then, to explore whether miR-490-3p would affect autophagy, apoptosis, and IR injury, we evaluated apoptosis, autophagy, and infarct size via gain- and loss-of-function experiments. Furthermore, we used adenovirus to enhance or inhibit the expression of ATG4B, and then measured autophagy, apoptosis, and IR injury. miR-490-3p was downregulated in the hearts during the process of IR, while ATG4B was upregulated. The inhibition of miR-490-3p or overexpression of ATG4B could promote the expression of LC3II, increase the autolysosomes, inhibit the expression of p62, and reduce infarct size. On all accounts, the inhibition of miR-490-3p could promote autophagy to reduce myocardial IR injury by upregulating ATG4B, a finding that provides new insights for the protective mechanism of autophagy in IR. Graphical Abstract.

摘要

我们研究了 miR-490-3p 在缺血再灌注(IR)损伤中的潜在作用。我们首先确定了 miR-490-3p 和自噬相关 4B 半胱氨酸(ATG4B)在 IR 中的表达。然后,为了探索 miR-490-3p 是否会影响自噬、细胞凋亡和 IR 损伤,我们通过增益和失能实验评估了细胞凋亡、自噬和梗死面积。此外,我们使用腺病毒增强或抑制 ATG4B 的表达,然后测量自噬、细胞凋亡和 IR 损伤。miR-490-3p 在 IR 过程中在心脏中下调,而 ATG4B 上调。抑制 miR-490-3p 或过表达 ATG4B 可以促进 LC3II 的表达,增加自噬体,抑制 p62 的表达,并减少梗死面积。总而言之,抑制 miR-490-3p 通过上调 ATG4B 促进自噬,从而减轻心肌 IR 损伤,这一发现为自噬在 IR 中的保护机制提供了新的见解。图表摘要。

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