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Arch Biochem Biophys. 2005 Jan 15;433(2):387-96.

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

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  • 1Department of Cell Biology, Dana-Farber Cancer Institute, Harvard Medical School, One Jimmy Fund Way, Boston, MA 02115, USA. christoph_handschin@dfci.harvard.edu <christoph_handschin@dfci.harvard.edu>

Abstract

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.

PMID:
15581595
[PubMed - indexed for MEDLINE]
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