Regulation of skeletal muscle mitochondrial function by nuclear receptors: implications for health and disease

被引:21
作者
Perez-Schindler, Joaquin [1 ]
Philp, Andrew [1 ]
机构
[1] Univ Birmingham, Sch Sport Exercise & Rehabil Sci, MRC ARUK Ctr Musculoskeletal Ageing Res, Birmingham, W Midlands, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
exercise; mitochondrial function; non-communicable disease; nuclear receptor; skeletal muscle; transcription factors; PROLIFERATOR-ACTIVATED-RECEPTOR; METABOLIC GENE-EXPRESSION; THYROID-HORMONE; TRANSCRIPTION FACTORS; OXIDATIVE-METABOLISM; CONTRACTILE ACTIVITY; ENERGY-METABOLISM; ORPHAN RECEPTOR; BETA; RESISTANCE;
D O I
10.1042/CS20150246
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Skeletal muscle metabolism is highly dependent on mitochondrial function, with impaired mitochondrial biogenesis associated with the development of metabolic diseases such as insulin resistance and type 2 diabetes. Mitochondria display substantial plasticity in skeletal muscle, and are highly sensitive to levels of physical activity. It is thought that physical activity promotes mitochondrial biogenesis in skeletal muscle through increased expression of genes encoded in both the nuclear and the mitochondrial genome; however, how this process is co-ordinated at the cellular level is poorly understood. Nuclear receptors (NRs) are key signalling proteins capable of integrating environmental factors and mitochondrial function, thereby providing a potential link between exercise and mitochondrial biogenesis. The aim of this review is to highlight the function of NRs in skeletal muscle mitochondrial biogenesis and discuss the therapeutic potential of NRs for the management and treatment of chronic metabolic disease.
引用
收藏
页码:589 / 599
页数:11
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