The multiple universes of estrogen-related receptor α and γ in metabolic control and related diseases

被引:125
作者
Audet-Walsh, Etienne [1 ]
Giguere, Vincent [1 ,2 ,3 ,4 ]
机构
[1] McGill Univ, Goodman Canc Res Ctr, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3G 1Y6, Canada
[4] McGill Univ, Dept Oncol, Montreal, PQ H3G 1Y6, Canada
基金
加拿大健康研究院;
关键词
diabetes; energy metabolism; fatty liver; glucose; metabolic syndrome; mitochondria; nuclear receptors; oxidative phosphorylation; skeletal muscle; PROLIFERATOR-ACTIVATED RECEPTOR; ERR-ALPHA; TRANSCRIPTIONAL CONTROL; BREAST-CANCER; SKELETAL-MUSCLE; GENE-EXPRESSION; OXIDATIVE-PHOSPHORYLATION; HEPATIC GLUCONEOGENESIS; INSULIN-RESISTANCE; ADIPOCYTE DIFFERENTIATION;
D O I
10.1038/aps.2014.121
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The identification of the estrogen-related receptors (ERRs) as the first orphan nuclear receptors ignited a new era in molecular endocrinology, which led to the discovery of new ligand-dependent response systems. Although ERR subfamily members have yet to be associated with a natural ligand, the characterization of these orphan receptors has demonstrated that they occupy a strategic node in the transcriptional control of cellular energy metabolism. In particular, ERRs are required for the response to various environmental challenges that require high energy levels by the organism. As central regulators of energy homeostasis, ERRs may also be implicated in the etiology of metabolic disorders, such as type 2 diabetes and metabolic syndrome. Here, we review the recent evidence that further highlights the role of ERRs in metabolic control, particularly in liver and skeletal muscle, and their likely involvement in metabolic diseases. Consequently, we also explore the promises and pitfalls of ERRs as potential therapeutic targets.
引用
收藏
页码:51 / 61
页数:11
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