河马信号通路
生物
线粒体生物发生
粒体自噬
细胞生物学
线粒体
自噬
品脱1
信号转导
细胞凋亡
遗传学
作者
Ying Tan,Lei Cai,Huifang Tang,Xiao Feng Zhu,Guanghui Yi
标识
DOI:10.1089/dna.2019.5348
摘要
Mitochondria serve as a hub for cell metabolism, energy production, and reactive oxygen species generation through multiple signaling pathways that control cardiomyocyte survival and death and contribute to the pathophysiological process of cardiovascular diseases (CVDs). Therefore, maintaining mitochondrial quality control (MQC) is essential for mitochondrial homeostasis and cardiac health. The Hippo pathway is a conserved signaling cascade that regulates mitochondrial function and cardiomyocyte fate and plays a crucial role in cardiac regeneration, repair, and diseases. MQC and the Hippo pathway are tightly coupled in CVDs, and several regulatory elements of the Hippo pathway directly/indirectly regulate mitochondria-related proteins to mediate mitochondrial morphology and function. In turn, mitochondrial morphology partly influences Hippo pathway function in the heart. This review outlines the underlying mechanisms by which the Hippo pathway regulates MQC from a variety of perspectives, including mitochondrial dynamics, mitophagy, mitochondrial biogenesis, mitochondrial apoptosis under oxidative stress, and mitochondrial metabolism. We also discuss the roles of the Hippo pathway in orchestrating mitochondria in CVDs, such as myocardial ischemia–reperfusion injury, septic cardiomyopathy, and diabetic cardiomyopathy, which may provide a novel therapeutic strategy.
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