ATF4
线粒体
综合应力响应
心肌病
细胞生物学
生物
线粒体DNA
医学
内科学
心力衰竭
未折叠蛋白反应
遗传学
翻译(生物学)
基因
信使核糖核酸
内质网
作者
Helen Huynh,Siting Zhu,Sharon Lee,Yutong Bao,Jing Pang,Anh Nguyen,Yusu Gu,Chao Chen,Kunfu Ouyang,Sylvia Μ. Evans,Xi Fang
标识
DOI:10.1016/j.yjmcc.2022.12.003
摘要
Mitochondrial dysfunction in heart triggers an integrated stress response (ISR) through phosphorylation of eIF2α and subsequent ATF4 activation. DAP3 Binding Cell Death Enhancer 1 (DELE1) is a mitochondrial protein recently found to be critical for mediating mitochondrial stress-triggered ISR (MSR)-induced eIF2α-ATF4 pathway activation. However, the specific role of DELE1 in heart at baseline or in response to mitochondrial stress remains largely unknown. In this study, we report that DELE1 is dispensable for cardiac development and function under baseline conditions. Conversely, DELE1 is essential for mediating an adaptive response to mitochondrial dysfunction-triggered stress in the heart, playing a protective role in mitochondrial cardiomyopathy.
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