Regulatory network of lipid-sensing nuclear receptors: roles for CAR, PXR, LXR, and FXR

被引:135
作者
Handschin, C
Meyer, UA
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Cell Biol, Boston, MA 02115 USA
[2] Univ Basel, Biozentrum, Div Pharmacol Neurobiol, CH-4056 Basel, Switzerland
关键词
nuclear receptors; drug-induction; lipids; bile acids; cholesterol; CAR; PXR; LXR; FXR; cytochrome P450;
D O I
10.1016/j.abb.2004.08.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cloning and characterization of the orphan nuclear receptors Constitutive androstane receptor (CAR, NR1I3) and pregnane X receptor (PXR, NR1I2) led to major breakthroughs in Studying drug-mediated transcriptional induction of drug-metabolizing cytochromes P450 (CYPs). More recently, additional roles for CAR and PXR have been discovered. As examples, these xenosensors are involved in the homeostasis of cholesterol, bile acids, bilirubin, and other endogenous hydrophobic molecules in the liver: CAR and PXR thus form an intricate regulatory network with other members of the nuclear receptor superfamily, foremost the cholesterol-sensing liver X receptor (LXR, NR1H2/3) and the bile-acid-activated farnesoid X receptor (FXR, NR1H4). In this review, functional interactions between these nuclear receptors as well as the consequences on physiology and pathophysiology of the liver are discussed. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:387 / 396
页数:10
相关论文
共 157 条
[1]   Dietary cholesterol fails to stimulate the human cholesterol 7α-hydroxylase gene (CYP7A1) in transgenic mice. [J].
Agellon, LB ;
Drover, VAB ;
Cheema, SK ;
Gbaguidi, GF ;
Walsh, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20131-20134
[2]   MODULATIONS IN HEPATIC BRANCH-POINT ENZYMES INVOLVED IN ISOPRENOID BIOSYNTHESIS UPON DIETARY AND DRUG TREATMENTS OF RATS [J].
ANDERSSON, M ;
ERICSSON, J ;
APPELKVIST, EL ;
SCHEDIN, S ;
CHOJNACKI, T ;
DALLNER, G .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1994, 1214 (01) :79-87
[3]   6α-hydroxylation of taurochenodeoxycholic acid and lithocholic acid by CYP3A4 in human liver microsomes [J].
Araya, Z ;
Wikvall, K .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 1999, 1438 (01) :47-54
[4]   Interactions between hepatic Mrp4 and Sult2a as revealed by the constitutive androstane receptor and Mrp4 knockout mice [J].
Assem, M ;
Schuetz, EG ;
Leggas, M ;
Sun, DX ;
Yasuda, K ;
Reid, G ;
Zelcer, N ;
Adachi, M ;
Strom, S ;
Evans, RM ;
Moore, DD ;
Borst, P ;
Schuetz, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (21) :22250-22257
[5]  
Auwerx J, 1999, CELL, V97, P161
[6]  
Aynaci FM, 2001, J CHILD NEUROL, V16, P367
[7]   PXR and the regulation of apoA1 and HDL-cholesterol in rodents [J].
Bachmann, K ;
Patel, H ;
Batayneh, Z ;
Slama, J ;
White, D ;
Posey, J ;
Ekins, S ;
Gold, D ;
Sambucetti, L .
PHARMACOLOGICAL RESEARCH, 2004, 50 (03) :237-246
[9]   Identification of a human nuclear receptor defines a new signaling pathway for CYP3A induction [J].
Bertilsson, G ;
Heidrich, J ;
Svensson, K ;
Åsman, M ;
Jendeberg, L ;
Sydow-Bäckman, M ;
Ohlsson, R ;
Postlind, H ;
Blomquist, P ;
Berkenstam, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (21) :12208-12213
[10]   CYTOCHROME-P450-2B ENZYME (CYP2B) INDUCTION DEFECT FOLLOWING PHENOBARBITAL TREATMENT IN THE FA/FA ZUCKER RAT - MOLECULAR CHARACTERIZATION [J].
BLOUIN, RA ;
BANDYOPADHYAY, AM ;
CHAUDHARY, I ;
ROBERTSON, LW ;
GEMZIK, B ;
PARKINSON, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 303 (02) :313-320