法尼甾体X受体
胆酸
鹅去氧胆酸
胆汁酸
孤儿受体
神经元源性孤儿受体1
G蛋白偶联胆汁酸受体
核受体
化学
生物化学
类固醇
肝X受体
核受体辅活化子2
脱氧胆酸
辅活化剂
小异二聚体伴侣
转录因子
孕烷X受体
肝受体同系物-1
CYP8B1
基因
激素
作者
Derek J. Parks,Steven G. Blanchard,Randy K. Bledsoe,Gyan Chandra,Thomas G. Consler,Steven A. Kliewer,Julie B. Stimmel,Timothy M. Willson,Ann Marie Zavacki,David D. Moore,Jürgen Lehmann
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1999-05-21
卷期号:284 (5418): 1365-1368
被引量:2036
标识
DOI:10.1126/science.284.5418.1365
摘要
Bile acids regulate the transcription of genes that control cholesterol homeostasis through molecular mechanisms that are poorly understood. Physiological concentrations of free and conjugated chenodeoxycholic acid, lithocholic acid, and deoxycholic acid activated the farnesoid X receptor (FXR; NR1H4), an orphan nuclear receptor. As ligands, these bile acids and their conjugates modulated interaction of FXR with a peptide derived from steroid receptor coactivator 1. These results provide evidence for a nuclear bile acid signaling pathway that may regulate cholesterol homeostasis.
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