Liver X Receptor Signaling Pathways and Atherosclerosis

被引:267
作者
Calkin, Anna C.
Tontonoz, Peter [1 ]
机构
[1] Univ Calif Los Angeles, Howard Hughes Med Inst, Sch Med, Los Angeles, CA 90095 USA
关键词
ATP-binding cassette transporter; atherosclerosis; lipoproteins; macrophages; BINDING CASSETTE TRANSPORTER-1; LXR-ALPHA; CHOLESTEROL EFFLUX; ENDOTHELIAL-CELLS; LIPID-METABOLISM; UP-REGULATION; AGONIST; EXPRESSION; T0901317; STRESS;
D O I
10.1161/ATVBAHA.109.191197
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
First discovered as orphan receptors, liver X receptors (LXRs) were subsequently identified as the nuclear receptor target of the cholesterol metabolites, oxysterols. There are 2 LXR receptors encoded by distinct genes: LXR alpha is most highly expressed in the liver, adipose, kidney, adrenal tissues, and macrophages and LXR alpha is ubiquitously expressed. Despite differential tissue distribution, these isoforms have 78% homology in their ligand-binding domain and appear to respond to the same endogenous ligands. Work over the past 10 years has shown that the LXR pathway regulates lipid metabolism and inflammation via both the induction and repression of target genes. Given the importance of cholesterol regulation and inflammation in the development of cardiovascular disease, it is not surprising that activation of the LXR pathway attenuates various mechanisms underlying atherosclerotic plaque development. In this brief review, we will discuss the impact of the LXR pathway on both cholesterol metabolism and atherosclerosis. (Arterioscler Thromb Vasc Biol. 2010;30:1513-1518.)
引用
收藏
页码:1513 / 1518
页数:6
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