抑制Setd7通过抑制脂质氧化来防止心肌细胞肥大。

IF 8.4 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Hai-Bi Su, Jing-Huan Wang, Yu-Yu Zhang, Jie Xu, Jia-Yao Liu, Yu-Hui Li, Chen-Xi Xiao, Cai-Yun Wang, Jun Chang, Xin-Hua Liu
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引用次数: 0

摘要

心肌肥厚是心力衰竭最显著的特征之一。SET结构域蛋白7 (Setd7)是一种负责组蛋白H3K4甲基化的催化酶,与多种心脏疾病有关。在这项研究中,我们调查了Setd7是否促进了心脏肥厚的发展。将雄性小鼠置于低压缺氧环境8周;新生儿大鼠心肌细胞(NRCMs)暴露于缺氧6小时。我们发现,缺氧刺激显著上调了nrcm中Setd7的表达水平以及肥厚标志物ANP和BNP的表达。通过功能丧失和功能获得实验,我们证明了Setd7可以调节缺氧心肌细胞中的肥厚和炎症标志物。我们进一步发现,setd7介导的E2F1 (E2启动子结合因子1)的激活触发了E3泛素蛋白连接酶WWP2的表达,该酶催化了谷胱甘肽过氧化物酶4 (GPx4)的泛素化和降解,GPx4是一种关键的脂质过氧化物还原酶。这种降解导致广泛的脂质过氧化,从而加剧病理性心脏肥厚。值得注意的是,ras选择性致死小分子3 (RSL3)对GPx4的抑制消除了Setd7敲低在心肌细胞中的抗肥厚作用,强调了脂质过氧化在Setd7介导的肥厚反应中的关键作用。综上所述,Setd7通过Setd7- e2f1 - wwp2 - gpx4信号通路促进缺氧诱导的心肌肥厚,提示靶向Setd7是缓解缺氧诱导的心肌肥厚的一种有前景的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of Setd7 protects against cardiomyocyte hypertrophy via inhibiting lipid oxidation.

Myocardial hypertrophy is one of the most prominent features of heart failure. SET domain-containing protein 7 (Setd7), a catalytic enzyme responsible for histone H3K4 methylation, has been implicated in various cardiac diseases. In this study we investigated whether Setd7 contributed to the development of cardiac hypertrophy. Male mice were subjected to a hypobaric hypoxic environment for 8 weeks; neonatal rat cardiomyocytes (NRCMs) exposed to hypoxia for 6 h. We showed that hypoxic stimulation significantly upregulated the expression levels of Setd7 along with the expression of hypertrophic markers ANP and BNP in NRCMs. By conducting loss- and gain-of-function assays, we demonstrated that Setd7 modulated the hypertrophic and inflammatory markers in hypoxic cardiomyocytes. We further revealed that Setd7-mediated activation of E2F1 (E2 promoter binding factor 1) triggered the expression of E3 ubiquitin protein ligases WWP2, which catalyzed the ubiquitination and degradation of glutathione peroxidase 4 (GPx4), a critical lipid peroxide-reducing enzyme. This degradation drove extensive lipid peroxidation, thereby exacerbating pathological cardiac hypertrophy. Notably, GPx4 inhibition by ras-selective lethal small molecule 3 (RSL3) abolished the antihypertrophic effects of Setd7 knockdown in cardiomyocytes, underscoring the pivotal role of lipid peroxidation in Setd7-mediated hypertrophic responses. In summary, Setd7 promotes hypoxia-induced cardiac hypertrophy through the Setd7-E2F1-WWP2-GPx4 signaling pathway, suggesting that targeting Setd7 is a promising therapeutic strategy to alleviate hypoxia-induced myocardial hypertrophy.

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来源期刊
Acta Pharmacologica Sinica
Acta Pharmacologica Sinica 医学-化学综合
CiteScore
15.10
自引率
2.40%
发文量
4365
审稿时长
2 months
期刊介绍: APS (Acta Pharmacologica Sinica) welcomes submissions from diverse areas of pharmacology and the life sciences. While we encourage contributions across a broad spectrum, topics of particular interest include, but are not limited to: anticancer pharmacology, cardiovascular and pulmonary pharmacology, clinical pharmacology, drug discovery, gastrointestinal and hepatic pharmacology, genitourinary, renal, and endocrine pharmacology, immunopharmacology and inflammation, molecular and cellular pharmacology, neuropharmacology, pharmaceutics, and pharmacokinetics. Join us in sharing your research and insights in pharmacology and the life sciences.
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