Bile acids: Natural ligands for an orphan nuclear receptor

被引:1906
作者
Parks, DJ
Blanchard, SG
Bledsoe, RK
Chandra, G
Consler, TG
Kliewer, SA
Stimmel, JB
Willson, TM [1 ]
Zavacki, AM
Moore, DD
Lehmann, JM
机构
[1] Glaxo Wellcome Inc, Res & Dev, Dept Med Chem, Res Triangle Pk, NC 27709 USA
[2] Glaxo Wellcome Inc, Res & Dev, Dept Mol Sci, Res Triangle Pk, NC 27709 USA
[3] Glaxo Wellcome Inc, Res & Dev, Dept Mol Biochem, Res Triangle Pk, NC 27709 USA
[4] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
关键词
D O I
10.1126/science.284.5418.1365
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
收藏
页码:1365 / 1368
页数:4
相关论文
共 31 条
[1]   Expression and transport properties of the human ileal and renal sodium-dependent bile acid transporter [J].
Craddock, AL ;
Love, MW ;
Daniel, RW ;
Kirby, LC ;
Walters, HC ;
Wong, MH ;
Dawson, PA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (01) :G157-G169
[2]   EFFECTS OF BILE-ACIDS AND STEROID/THYROID HORMONES ON THE EXPRESSION OF CHOLESTEROL 7-ALPHA-HYDROXYLASE MESSENGER-RNA AND THE CYP7 GENE IN HEPG2 CELLS [J].
CRESTANI, M ;
KARAM, WG ;
CHIANG, JYL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 198 (02) :546-553
[3]  
DICKSON EFG, 1995, J PHOTOCH PHOTOBIO B, V27, P3
[4]   IDENTIFICATION OF A NUCLEAR RECEPTOR THAT IS ACTIVATED BY FARNESOL METABOLITES [J].
FORMAN, BM ;
GOODE, E ;
CHEN, J ;
ORO, AE ;
BRADLEY, DJ ;
PERLMANN, T ;
NOONAN, DJ ;
BURKA, LT ;
MCMORRIS, T ;
LAMPH, WW ;
EVANS, RM ;
WEINBERGER, C .
CELL, 1995, 81 (05) :687-693
[5]   MOLECULAR-CLONING, EXPRESSION, AND CHARACTERIZATION OF A HUMAN INTESTINAL 15-KDA PROTEIN [J].
FUJITA, M ;
FUJII, H ;
KANDA, T ;
SATO, E ;
HATAKEYAMA, K ;
ONO, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 233 (02) :406-413
[6]   Nuclear receptor coactivators [J].
Glass, CK ;
Rose, DW ;
Rosenfeld, MG .
CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (02) :222-232
[7]   MOLECULAR-CLONING, TISSUE DISTRIBUTION, AND EXPRESSION OF A 14-KDA BILE ACID-BINDING PROTEIN FROM RAT ILEAL CYTOSOL [J].
GONG, YZ ;
EVERETT, ET ;
SCHWARTZ, DA ;
NORRIS, JS ;
WILSON, FA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (11) :4741-4745
[8]   A signature motif in transcriptional co-activators mediates binding to nuclear receptor [J].
Heery, DM ;
Kalkhoven, E ;
Hoare, S ;
Parker, MG .
NATURE, 1997, 387 (6634) :733-736
[9]   Effect of bile on the intestinal bile-acid binding protein (I-BABP) expression. In vitro and in vivo studies [J].
Kanda, T ;
Niot, I ;
Foucaud, L ;
Fujii, H ;
Bernard, A ;
Ono, T ;
Besnard, P .
FEBS LETTERS, 1996, 384 (02) :131-134
[10]   Regulation of expression of human intestinal bile acid-binding protein in Caco-2 cells [J].
Kanda, T ;
Foucand, L ;
Nakamura, Y ;
Niot, I ;
Besnard, P ;
Fujita, M ;
Sakai, Y ;
Hatakeyama, K ;
Ono, T ;
Fujii, H .
BIOCHEMICAL JOURNAL, 1998, 330 :261-265