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硫氧还蛋白2在心力衰竭中的作用机制

Mechanistic Role of Thioredoxin 2 in Heart Failure.

作者信息

Chen Chaofei, Chen Haixuan, Zhou Huanjiao Jenny, Ji Weidong, Min Wang

机构信息

The First Affiliated Hospital, Center for Translational Medicine, Sun Yat-sen University, Guangzhou, China.

Interdepartmental Program in Vascular Biology and Therapeutics, Department of Pathology, Yale University School of Medicine, 10 Amistad St, 401B, New Haven, CT, 06520, USA.

出版信息

Adv Exp Med Biol. 2017;982:265-276. doi: 10.1007/978-3-319-55330-6_14.

Abstract

Thioredoxin 2 (Trx2) is a pivotal mitochondrial protein that regulates redox signaling. The mitochondrial Trx2 is expressed ubiquitously, but it is found at the highest levels in metabolically active tissues like the heart. Global gene knockout of Trx2 results in embryonic lethality, likely due to the increased cellular oxidative stress. Moreover, mice with cardiac-specific Trx2 deletion develop spontaneous dilated cardiomyopathy (DCM), correlating with increased apoptosis stress kinase-1 (ASK1) signaling and increased cardiomyocyte apoptosis. Cardiomyocyte apoptosis is a common mechanism in the pathogenesis of heart failure. Our results show that Trx2 is essential for maintaining cardiac function. In this chapter, we summarize the key mechanistic role of Trx2 in preserving cardiac function by suppressing mitochondrial reactive oxygen species (ROS) generation and by inhibiting ASK1-dependent apoptosis in heart failure. Trx2 and ASK1 represent promising targets to develop therapeutic strategies for the treatment of DCM and heart failure.

摘要

硫氧还蛋白2(Trx2)是一种调节氧化还原信号的关键线粒体蛋白。线粒体Trx2在全身广泛表达,但在心脏等代谢活跃组织中含量最高。Trx2的全基因敲除会导致胚胎致死,这可能是由于细胞氧化应激增加所致。此外,心脏特异性缺失Trx2的小鼠会发生自发性扩张型心肌病(DCM),这与凋亡应激激酶-1(ASK1)信号增加和心肌细胞凋亡增加相关。心肌细胞凋亡是心力衰竭发病机制中的一个常见机制。我们的结果表明,Trx2对维持心脏功能至关重要。在本章中,我们总结了Trx2在心力衰竭中通过抑制线粒体活性氧(ROS)生成和抑制ASK1依赖性凋亡来维持心脏功能的关键机制作用。Trx2和ASK1是开发治疗DCM和心力衰竭治疗策略的有前景的靶点。

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