DELE1 is Protective for Mitochondrial Cardiomyopathy
- Huynh, Helen
- Advisor(s): Fang, Xi;
- Niwa, Maho
Abstract
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 and acquired cardiomyopathy 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. We also found that DELE1 cKO mice exhibit similar cardiac structure and function, compared with controls, in response to pressure overload-induced heart failure.