An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway

被引:1344
作者
Kliewer, SA [1 ]
Moore, JT
Wade, L
Staudinger, JL
Watson, MA
Jones, SA
McKee, DD
Oliver, BB
Willson, TM
Zetterström, RH
Perlmann, T
Lehmann, JM
机构
[1] Glaxo Wellcome Res & Dev Ltd, Dept Mol Endocrinol, Res Triangle Pk, NC 27709 USA
[2] Glaxo Wellcome Res & Dev Ltd, Dept Mol Sci, Res Triangle Pk, NC 27709 USA
[3] Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA
[4] Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden
[5] Ludwig Inst Canc Res, Stockholm Branch, S-17177 Stockholm, Sweden
关键词
D O I
10.1016/S0092-8674(00)80900-9
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
Steroid hormones exert profound effects on differentiation, development, and homeostasis in higher eukaryotes through interactions with nuclear receptors. We describe a novel orphan nuclear receptor, termed the pregnane X receptor (PXR), that is activated by naturally occurring steroids such as pregnenolone and progesterone, and synthetic glucocorticoids and antiglucocorticoids. PXR exists as two isoforms, PXR.1 and PXR.2, that are differentially activated by steroids. Notably, PXR.1 is efficaciously activated by pregnenolone 16 alpha-carbonitrile, a glucocorticoid receptor antagonist that induces the expression of the CYP3A family of steroid hydroxylases and modulates sterol and bile acid biosynthesis in vivo. Our results provide evidence for the existence of a novel steroid hormone signaling pathway with potential implications in the regulation of steroid hormone and sterol homeostasis.
引用
收藏
页码:73 / 82
页数:10
相关论文
共 57 条
[1]   CLONING AND EXPRESSION OF FULL-LENGTH CDNA-ENCODING HUMAN VITAMIN-D RECEPTOR [J].
BAKER, AR ;
MCDONNELL, DP ;
HUGHES, M ;
CRISP, TM ;
MANGELSDORF, DJ ;
HAUSSLER, MR ;
PIKE, JW ;
SHINE, J ;
OMALLEY, BW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (10) :3294-3298
[2]   STEROID-HORMONE RECEPTORS - MANY ACTORS IN SEARCH OF A PLOT [J].
BEATO, M ;
HERRLICH, P ;
SCHUTZ, G .
CELL, 1995, 83 (06) :851-857
[3]  
Cadepond F, 1997, ANNU REV MED, V48, P129
[4]   MOLECULAR-CLONING OF HUMAN AND RAT COMPLEMENTARY-DNA ENCODING ANDROGEN RECEPTORS [J].
CHANG, CS ;
KOKONTIS, J ;
LIAO, SS .
SCIENCE, 1988, 240 (4850) :324-326
[5]   SENSITIVE MESSENGER-RNA DETECTION USING UNFIXED TISSUE - COMBINED RADIOACTIVE AND NONRADIOACTIVE INSITU HYBRIDIZATION HISTOCHEMISTRY [J].
DAGERLIND, A ;
FRIBERG, K ;
BEAN, AJ ;
HOKFELT, T .
HISTOCHEMISTRY, 1992, 98 (01) :39-49
[6]   Distribution and induction of CYP3A1 and CYP3A2 in rat liver and extrahepatic tissues [J].
Debri, K ;
Boobis, AR ;
Edwards, RJ .
BIOCHEMICAL PHARMACOLOGY, 1995, 50 (12) :2047-2056
[7]  
ELSHOURBAGY NA, 1980, J BIOL CHEM, V255, P1279
[8]   Orphan nuclear receptors - The first eight years [J].
Enmark, E ;
Gustafsson, JA .
MOLECULAR ENDOCRINOLOGY, 1996, 10 (11) :1293-1307
[9]   THE STEROID AND THYROID-HORMONE RECEPTOR SUPERFAMILY [J].
EVANS, RM .
SCIENCE, 1988, 240 (4854) :889-895
[10]   Hypolipidemic drugs, polyunsaturated fatty acids, and eicosanoids are ligands for peroxisome proliferator-activated receptors alpha and delta [J].
Forman, BM ;
Chen, J ;
Evans, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4312-4317