Mitochondrial Quality Control in COPD and IPF

被引:68
作者
Hara, Hiromichi [1 ]
Kuwano, Kazuyoshi [1 ]
Araya, Jun [1 ]
机构
[1] Jikei Univ, Sch Med, Dept Internal Med, Div Resp Dis, Tokyo 1058461, Japan
关键词
mitochondria; mitochondria dynamics; mitophagy; chronic obstructive pulmonary disease (COPD); idiopathic pulmonary fibrosis (IPF); CELLULAR SENESCENCE; PULMONARY-FIBROSIS; PARK2-MEDIATED MITOPHAGY; INFLAMMATORY RESPONSES; OXIDATIVE STRESS; PATHOGENESIS; AUTOPHAGY; OPA1; DYSFUNCTION; DISEASE;
D O I
10.3390/cells7080086
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondria play important roles in the maintenance of intracellular homeostasis; hence, the quality control of mitochondria is crucial for cell fate determination. Mitochondria dynamics and mitochondria-specific autophagy, known as mitophagy, are two main quality control systems in cells. Mitochondria fuse to increase energy production in response to stress, and damaged mitochondria are segregated by fission and degraded by mitophagy. Once these systems are disrupted, dysfunctional mitochondria with decreased adenosine triphosphate (ATP) production and increased reactive oxygen species (ROS) production accumulate, affecting cell fate. Recently, increasing evidence suggests that the dysregulation of mitochondria quality control is pathogenic in several age-related diseases. In this review, we outlined the role of mitochondria quality control systems in the pathogenesis of age-associated lung diseases, chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF).
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页数:13
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