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METTL3、m6A修饰与早期生长反应蛋白1(EGR1):影响心肌缺血/再灌注损伤结果的相互作用

METTL3, m6A modification, and EGR1: interplay affecting myocardial I/R injury outcomes.

作者信息

Huang Chen, Zhang Xun, Wu Shi-Xiong, Chang Qing, Zheng Zhi-Kun, Xu Jing

机构信息

Department of Cardiovascular Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450000, China.

出版信息

Cell Biol Toxicol. 2024 Dec 21;41(1):7. doi: 10.1007/s10565-024-09937-7.

Abstract

The occurrence of severe myocardial ischemia/reperfusion (I/R) injury is associated with the clinical application of reestablishment technique for heart disease, and understanding its underlying mechanisms is currently an urgent issue. Prior investigations have demonstrated the potential enhancement of MIRI through EGR1 suppression, although the precise underlying regulatory pathways require further elucidation. The core focus of this investigation is to examine the molecular pathways through EGR1 regulates mitophagy-mediated myocardial cell pyroptosis and its impact on MIRI. Cardiomyocyte hypoxia/reoxygenation (H/R) injury models and mouse models of myocardial I/R injury were used to investigate the involvement of EGR1 in regulating mitophagy-mediated myocardial cell pyroptosis in myocardial I/R injury. The research outcomes demonstrated that under H/R conditions, EGR1 expression was upregulated and inhibited the JAK2/STAT3 pathway, leading to enhanced mitophagy and disrupted mitochondrial fusion/fission dynamics, ultimately resulting in myocardial cell pyroptosis. Further research revealed that the upregulation of EGR1 expression was mediated by methyltransferase like 3 (METTL3)-mediated m6A modification of EGR1 mRNA and depended on the binding of insulin like growth factor 2 mrna binding protein 2 (IGF2BP2) to the N6-methyladenosine (m6A) modification site to enhance mRNA stability. In vivo animal experiments confirmed that METTL3 upregulated EGR1 expression through IGF2BP2 and suppressed activation of the janus kinase 2 (JAK2) /signal transducer and activator of transcription 3 (STAT3) pathway, thereby inhibiting mitophagy, disrupting mitochondrial dynamics, promoting myocardial cell pyroptosis, and exacerbating I/R injury.

摘要

严重心肌缺血/再灌注(I/R)损伤的发生与心脏病重建技术的临床应用相关,了解其潜在机制是当前亟待解决的问题。先前的研究表明,通过抑制早期生长反应蛋白1(EGR1)可能会加重心肌缺血再灌注损伤(MIRI),尽管其确切的潜在调控途径仍需进一步阐明。本研究的核心重点是探讨EGR1通过何种分子途径调节线粒体自噬介导的心肌细胞焦亡及其对MIRI的影响。利用心肌细胞缺氧/复氧(H/R)损伤模型和心肌I/R损伤小鼠模型,研究EGR1在心肌I/R损伤中调节线粒体自噬介导的心肌细胞焦亡的作用。研究结果表明,在H/R条件下,EGR1表达上调并抑制JAK2/STAT3通路,导致线粒体自噬增强,线粒体融合/分裂动力学紊乱,最终导致心肌细胞焦亡。进一步研究发现,EGR1表达上调是由甲基转移酶样3(METTL3)介导的EGR1 mRNA的m6A修饰介导的,并依赖于胰岛素样生长因子2 mRNA结合蛋白2(IGF2BP2)与N6-甲基腺苷(m6A)修饰位点的结合来增强mRNA稳定性。体内动物实验证实,METTL3通过IGF2BP2上调EGR1表达,抑制Janus激酶2(JAK2)/信号转导和转录激活因子3(STAT3)通路的激活,从而抑制线粒体自噬,破坏线粒体动力学,促进心肌细胞焦亡,加重I/R损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4987/11662061/b0eb989b6d3f/10565_2024_9937_Fig1_HTML.jpg

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