The beneficial role of proteolysis in skeletal muscle growth and stress adaptation

被引:83
作者
Bell, Ryan A. V. [1 ,2 ]
Al-Khalaf, Mohammad [1 ,2 ]
Megeney, Lynn A. [1 ,2 ,3 ]
机构
[1] Ottawa Hosp, Ottawa Hosp Res Inst, Sprott Ctr Stem Cell Res, Regenerat Med Program, Ottawa, ON K1H 8L6, Canada
[2] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
[3] Univ Ottawa, Dept Med, Div Cardiol, Ottawa, ON, Canada
来源
SKELETAL MUSCLE | 2016年 / 6卷
基金
加拿大健康研究院;
关键词
Proteolysis; Proteasome; Autophagy; Caspase; Muscle growth; Muscle cell differentiation; UBIQUITIN-PROTEASOME SYSTEM; PROTEIN-DEGRADATION; MYOGENIC DIFFERENTIATION; MITOCHONDRIAL DYSFUNCTION; CELL-DIFFERENTIATION; MUSCULAR-DYSTROPHY; CASPASE ACTIVATION; INDUCED AUTOPHAGY; SATELLITE CELLS; ACUTE EXERCISE;
D O I
10.1186/s13395-016-0086-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Muscle atrophy derived from excessive proteolysis is a hallmark of numerous disease conditions. Accordingly, the negative consequences of skeletal muscle protein breakdown often overshadow the critical nature of proteolytic systems in maintaining normal cellular function. Here, we discuss the major cellular proteolysis machinery-the ubiquitin/proteosome system, the autophagy/lysosomal system, and caspase-mediated protein cleavage- and the critical role of these protein machines in establishing and preserving muscle health. We examine how ordered degradation modifies (1) the spatiotemporal expression of myogenic regulatory factors during myoblast differentiation, (2) membrane fusion during myotube formation, (3) sarcomere remodeling and muscle growth following physical stress, and (4) energy homeostasis during nutrient deprivation. Finally, we review the origin and etiology of a number of myopathies and how these devastating conditions arise from inborn errors in proteolysis.
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页数:13
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