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PMID: 12690094 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Liver X receptor signaling pathways in cardiovascular disease.

Molecular endocrinology (Baltimore, Md.) ·Vol. 17 ·No. 6 ·2003-06-00 ·Pages 985-93

Tontonoz P, Mangelsdorf DJ

Abstract

The liver X receptors alpha and beta (LXRalpha and LXRbeta) are members of the nuclear receptor family of proteins that are critical for the control of lipid homeostasis in vertebrates. The endogenous activators of these receptors are oxysterols and intermediates in the cholesterol biosynthetic pathway. LXRs serve as cholesterol sensors that regulate the expression of multiple genes involved in the efflux, transport, and excretion of cholesterol. Recent studies have outlined the importance of LXR signaling pathways in the development of metabolic disorders such as hyperlipidemia and atherosclerosis. Synthetic LXR agonists inhibit the development of atherosclerosis in murine models, an effect that is likely to result from the modulation of both metabolic and inflammatory gene expression. These observations identify the LXR pathway as a potential target for therapeutic intervention in human cardiovascular disease.

MeSH Terms
ATP-Binding Cassette Transporters/metabolism Animals Apolipoproteins/metabolism Cardiovascular Diseases/physiopathology,prevention & control Cholesterol/metabolism DNA-Binding Proteins Humans Liver X Receptors Mice Orphan Nuclear Receptors Receptors, Cytoplasmic and Nuclear/metabolism Signal Transduction/physiology
Chemicals
ATP-Binding Cassette Transporters Apolipoproteins DNA-Binding Proteins Liver X Receptors NR1H3 protein, human Nr1h3 protein, mouse Orphan Nuclear Receptors Receptors, Cytoplasmic and Nuclear Cholesterol
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tontonoz Peter
Howard Hughes Medical Institute, University of California, Los Angeles School of Medicine, Box 951662, Los Angeles, California 90095-1662, USA. ptontonoz@mednet.ucla.edu
Mangelsdorf David J
Article Info
Journal
Molecular endocrinology (Baltimore, Md.)
Abbr.
Mol Endocrinol
ISSN
0888-8809
Published
2003-06-00
Epub
2003-00-10
Pages
985-93
Language
English
Region
United States
NLM ID
8801431
Subset
IM
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