METTL3、m6A修饰和EGR1:影响心肌I/R损伤结局的相互作用

IF 5.3 2区 医学 Q2 CELL BIOLOGY
Chen Huang, Xun Zhang, Shi-Xiong Wu, Qing Chang, Zhi-Kun Zheng, Jing Xu
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引用次数: 0

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有关,了解其潜在机制是当前迫切需要解决的问题。先前的研究已经证明了通过抑制EGR1可能增强MIRI,尽管确切的潜在调控途径需要进一步阐明。本研究的核心重点是研究EGR1通过调节有丝分裂介导的心肌细胞焦亡的分子途径及其对MIRI的影响。采用心肌细胞缺氧/再氧合(H/R)损伤模型和小鼠心肌I/R损伤模型,探讨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,抑制JAK2/STAT3通路,导致线粒体自噬增强,线粒体融合/裂变动力学被破坏,最终导致心肌细胞焦亡。进一步研究发现,EGR1表达上调是通过甲基转移酶样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)结合n6 -甲基腺苷(m6A)修饰位点增强mRNA稳定性。体内动物实验证实,METTL3通过IGF2BP2上调EGR1的表达,抑制janus kinase 2 (JAK2) /signal transducer and activator of transcription 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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
METTL3, m6A modification, and EGR1: interplay affecting myocardial I/R injury outcomes.

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.

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来源期刊
Cell Biology and Toxicology
Cell Biology and Toxicology 生物-毒理学
CiteScore
9.90
自引率
4.90%
发文量
101
审稿时长
>12 weeks
期刊介绍: Cell Biology and Toxicology (CBT) is an international journal focused on clinical and translational research with an emphasis on molecular and cell biology, genetic and epigenetic heterogeneity, drug discovery and development, and molecular pharmacology and toxicology. CBT has a disease-specific scope prioritizing publications on gene and protein-based regulation, intracellular signaling pathway dysfunction, cell type-specific function, and systems in biomedicine in drug discovery and development. CBT publishes original articles with outstanding, innovative and significant findings, important reviews on recent research advances and issues of high current interest, opinion articles of leading edge science, and rapid communication or reports, on molecular mechanisms and therapies in diseases.
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