法尼甾体X受体
胆固醇7α羟化酶
CYP8B1
G蛋白偶联胆汁酸受体
胆汁酸
CYP27A1
生物化学
肝肠循环
核受体
分解代谢
运输机
化学
胆固醇逆向转运
胆固醇
肝受体同系物-1
酶
氨基酸
孕烷X受体
基因
转录因子
脂蛋白
作者
Makoto Makishima,Arthur Y. Okamoto,Joyce J. Repa,Hua Tu,R. Marc Learned,Alvin Luk,Mitchell Hull,Kevin D. Lustig,David J. Mangelsdorf,Bei Shan
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1999-05-21
卷期号:284 (5418): 1362-1365
被引量:2566
标识
DOI:10.1126/science.284.5418.1362
摘要
Bile acids are essential for the solubilization and transport of dietary lipids and are the major products of cholesterol catabolism. Results presented here show that bile acids are physiological ligands for the farnesoid X receptor (FXR), an orphan nuclear receptor. When bound to bile acids, FXR repressed transcription of the gene encoding cholesterol 7α-hydroxylase, which is the rate-limiting enzyme in bile acid synthesis, and activated the gene encoding intestinal bile acid–binding protein, which is a candidate bile acid transporter. These results demonstrate a mechanism by which bile acids transcriptionally regulate their biosynthesis and enterohepatic transport.
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