法尼甾体X受体
G蛋白偶联胆汁酸受体
生物
肝X受体
氧甾醇
胆汁酸
交易激励
核受体
胆固醇7α羟化酶
鹅去氧胆酸
调节器
内生
生物化学
胆固醇
CYP8B1
孕烷X受体
辅活化剂
小异二聚体伴侣
细胞生物学
转录因子
基因
作者
Haibo Wang,Jasmine Chen,Kevin Hollister,Lawrence C. Sowers,Barry M. Forman
出处
期刊:Molecular Cell
[Elsevier]
日期:1999-05-01
卷期号:3 (5): 543-553
被引量:1403
标识
DOI:10.1016/s1097-2765(00)80348-2
摘要
The major metabolic pathway for elimination of cholesterol is via conversion to bile acids. In addition to this metabolic function, bile acids also act as signaling molecules that negatively regulate their own biosynthesis. However, the precise nature of this signaling pathway has been elusive. We have isolated an endogenous biliary component (chenodeoxycholic acid) that selectively activates the orphan nuclear receptor, FXR. Structure–activity analysis defined a subset of related bile acid ligands that activate FXR and promote coactivator recruitment. Finally, we show that ligand-occupied FXR inhibits transactivation from the oxysterol receptor LXRα, a positive regulator of cholesterol degradation. We suggest that FXR (BAR) is the endogenous bile acid sensor and thus an important regulator of cholesterol homeostasis.
科研通智能强力驱动
Strongly Powered by AbleSci AI