线粒体
生物能学
自噬
细胞生物学
生物
氧化磷酸化
细胞器
程序性细胞死亡
活性氧
氧化应激
线粒体融合
线粒体DNA
细胞凋亡
生物化学
基因
作者
John S. Harrington,Stefan W. Ryter,Maria Plataki,David R. Price,Augustine M.K. Choi
出处
期刊:Physiological Reviews
[American Physiological Society]
日期:2023-04-06
卷期号:103 (4): 2349-2422
被引量:161
标识
DOI:10.1152/physrev.00058.2021
摘要
Mitochondria are well known as organelles responsible for the maintenance of cellular bioenergetics through the production of ATP. Although oxidative phosphorylation may be their most important function, mitochondria are also integral for the synthesis of metabolic precursors, calcium regulation, the production of reactive oxygen species, immune signaling, and apoptosis. Considering the breadth of their responsibilities, mitochondria are fundamental for cellular metabolism and homeostasis. Appreciating this significance, translational medicine has begun to investigate how mitochondrial dysfunction can represent a harbinger of disease. In this review, we provide a detailed overview of mitochondrial metabolism, cellular bioenergetics, mitochondrial dynamics, autophagy, mitochondrial damage-associated molecular patterns, mitochondria-mediated cell death pathways, and how mitochondrial dysfunction at any of these levels is associated with disease pathogenesis. Mitochondria-dependent pathways may thereby represent an attractive therapeutic target for ameliorating human disease.
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