骨骼肌
线粒体融合
线粒体
氧化磷酸化
细胞生物学
肌肉萎缩
生物
心肌
萎缩
细胞器
调节器
内科学
内分泌学
生物化学
医学
线粒体DNA
基因
遗传学
作者
John Noone,Donal J. OʼGorman,Helena Kenny
标识
DOI:10.1016/j.tem.2022.07.003
摘要
The mitochondria are double-membrane organelles integral for energy metabolism. Mitochondrial dynamics is regulated by inner and outer mitochondrial membrane (IMM and OMM) proteins, which promote fission and fusion. Optic atrophy 1 (OPA1) regulates IMM fusion, prevents apoptosis, and is a key regulator of morphological change in skeletal and cardiac muscle physiology and pathophysiology. OPA1 fuses the inner membranes of adjacent mitochondria, allowing for an increase in oxidative phosphorylation (OXPHOS). Considering the importance of energy metabolism in whole-body physiology, OPA1 and its regulators have been proposed as novel targets for the treatment of skeletal muscle atrophy and heart failure. Here, we review the role and regulation of OPA1 in skeletal muscle and cardiac pathophysiology, epitomizing its critical role in the cell.
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