Estrogen-related Receptor Signaling in Skeletal Muscle Fitness

被引:2
|
作者
Sopariwala, Danesh [1 ]
Nguyen, Hao [1 ]
Narkar, Vihang [1 ,2 ]
机构
[1] Univ Texas John P & Katherine G McGovern Med Sch, Inst Mol Med, Houston, TX 77030 USA
[2] Univ Texas John P & Katherine G McGovern Med Sch, Mol Med 1825 Pressler St, Houston, TX 77030 USA
关键词
nuclear receptors; transcription; exercise; metabolism; angiogenesis; regeneration; PROLIFERATOR-ACTIVATED RECEPTOR; ALPHA ERR-ALPHA; PHOSPHORYLATION-DEPENDENT SUMOYLATION; DUCHENNE MUSCULAR-DYSTROPHY; PDK4; GENE-EXPRESSION; BREAST-CANCER CELLS; TRANSCRIPTIONAL CONTROL; MITOCHONDRIAL BIOGENESIS; ENERGY-EXPENDITURE; INSULIN-RESISTANCE;
D O I
10.1055/a-2035-8192
中图分类号
G8 [体育];
学科分类号
04 ; 0403 ;
摘要
Skeletal muscle is a highly plastic tissue that can alter its metabolic and contractile features, as well as regenerative potential in response to exercise and other conditions. Multiple signaling factors including metabolites, kinases, receptors, and transcriptional factors have been studied in the regulation of skeletal muscle plasticity. Recently, estrogen-related receptors (ERRs) have emerged as a critical transcriptional hub in control of skeletal muscle homeostasis. ERRa and ERR? - the two highly expressed ERR sub-types in the muscle respond to various extracellular cues such as exercise, hypoxia, fasting and dietary factors, in turn regulating gene expression in the skeletal muscle. On the other hand, conditions such as diabetes and muscular dystrophy suppress expression of ERRs in the skeletal muscle, likely contributing to disease progression. We highlight key functions of ERRs in the skeletal muscle including the regulation of fiber type, mitochondrial metabolism, vascularization, and regeneration. We also describe how ERRs are regulated in the skeletal muscle, and their interaction with important muscle regulators (e. g. AMPK and PGCs). Finally, we identify critical gaps in our understanding of ERR signaling in the skeletal muscle, and suggest future areas of investigation to advance ERRs as potential targets for function promoting therapeutics in muscle diseases.
引用
收藏
页码:609 / 617
页数:9
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