Makishima M, Okamoto A Y, Repa J J, Tu H, Learned R M, Luk A, Hull M V, Lustig K D, Mangelsdorf D J, Shan B
Howard Hughes Medical Institute and Department of Pharmacology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75235-9050, USA.
Science. 1999 May 21;284(5418):1362-5. doi: 10.1126/science.284.5418.1362.
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 7alpha-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.
胆汁酸对于膳食脂质的溶解和运输至关重要,并且是胆固醇分解代谢的主要产物。此处呈现的结果表明,胆汁酸是法尼醇X受体(FXR,一种孤儿核受体)的生理性配体。当与胆汁酸结合时,FXR抑制编码胆固醇7α-羟化酶(胆汁酸合成中的限速酶)的基因的转录,并激活编码肠胆汁酸结合蛋白(一种候选胆汁酸转运蛋白)的基因。这些结果证明了一种胆汁酸对其生物合成和肠肝循环运输进行转录调控的机制。