Mitochondrial Dysfunction as an Underlying Cause of Skeletal Muscle Disorders

被引:34
|
作者
Chen, Tsung-Hsien [1 ]
Koh, Kok-Yean [2 ]
Lin, Kurt Ming-Chao [3 ]
Chou, Chu-Kuang [2 ,4 ]
机构
[1] Chia Yi Christian Hosp, Ditmanson Med Fdn, Dept Internal Med, Chiayi 60002, Taiwan
[2] Chia Yi Christian Hosp, Ditmanson Med Fdn, Dept Internal Med, Div Gastroenterol & Hepatol, Chiayi 60002, Taiwan
[3] Natl Hlth Res Inst, Inst Biomed Engn & Nanomed, Zhunan 35053, Taiwan
[4] Chia Yi Christian Hosp, Ditmanson Med Fdn, Obes Ctr, Chiayi 60002, Taiwan
关键词
mitochondrial dysfunction; skeletal muscle disorders; OXPHOS; mtDNA mutation; mitochondrial dynamics; mitophagy; mitochondrial chaperone protein; OXIDATIVE STRESS; GENE-EXPRESSION; DNA-DELETION; EXERCISE; AUTOPHAGY; PHOSPHORYLATION; TRANSCRIPTION; CALCIUM; ATROPHY; ACTIVATION;
D O I
10.3390/ijms232112926
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria are an important energy source in skeletal muscle. A main function of mitochondria is the generation of ATP for energy through oxidative phosphorylation (OXPHOS). Mitochondrial defects or abnormalities can lead to muscle disease or multisystem disease. Mitochondrial dysfunction can be caused by defective mitochondrial OXPHOS, mtDNA mutations, Ca2+ imbalances, mitochondrial-related proteins, mitochondrial chaperone proteins, and ultrastructural defects. In addition, an imbalance between mitochondrial fusion and fission, lysosomal dysfunction due to insufficient biosynthesis, and/or defects in mitophagy can result in mitochondrial damage. In this review, we explore the association between impaired mitochondrial function and skeletal muscle disorders. Furthermore, we emphasize the need for more research to determine the specific clinical benefits of mitochondrial therapy in the treatment of skeletal muscle disorders.
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页数:19
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