Sterol Regulation of Metabolism, Homeostasis, and Development

被引:110
|
作者
Wollam, Joshua [1 ,2 ,3 ]
Antebi, Adam [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Huffington Ctr Aging, Houston, TX 77030 USA
[2] Baylor Coll Med, Interdept Program Cell & Mol Biol, Houston, TX 77030 USA
[3] Max Planck Inst Biol Ageing, D-50931 Cologne, Germany
来源
关键词
hormones; endocrine signaling; life span; aging; reproduction; diapause; LIVER-X-RECEPTOR; CONSTITUTIVE ANDROSTANE RECEPTOR; VITAMIN-D-RECEPTOR; NEMATODE CAENORHABDITIS-ELEGANS; ORPHAN NUCLEAR RECEPTOR; BILE-ACID SYNTHESIS; INTRACELLULAR CHOLESTEROL TRAFFICKING; PROTEIN GENE-EXPRESSION; ELEMENT-BINDING PROTEIN; DAUER LARVA FORMATION;
D O I
10.1146/annurev-biochem-081308-165917
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
Sterol metabolites are critical signaling molecules that regulate metabolism, development, and homeostasis. Oxysterols, bile acids (BAs), and steroids work primarily through cognate sterol-responsive nuclear hormone receptors to control these processes through feed-forward and feedback mechanisms. These signaling pathways are conserved from simple invertebrates to mammals. Indeed, results from various model organisms have yielded fundamental insights into cholesterol and BA homeostasis, lipid and glucose metabolism, protective mechanisms, tissue differentiation, development, reproduction, and even aging. Here, we review how sterols act through evolutionarily ancient mechanisms to control these processes.
引用
收藏
页码:885 / 916
页数:32
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