PPARγ promotes monocyte/macrophage differentiation and uptake of oxidized LDL

被引:1616
作者
Tontonoz, P
Nagy, L
Alvarez, JGA
Thomazy, VA
Evans, RM [1 ]
机构
[1] Howard Hughes Med Inst, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, La Jolla, CA 92037 USA
[3] Univ Calif San Diego, Dept Pathol, La Jolla, CA 92093 USA
[4] Univ Texas, Sch Med, Dept Pathol, Houston, TX 77225 USA
[5] Univ Texas, Sch Med, Dept Integrat Biol, Houston, TX 77225 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(00)81575-5
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
The formation of foam cells from macrophages in the arterial wall is characterized by dramatic changes in lipid metabolism, including increased expression of scavenger receptors and the uptake of oxidized low-density lipoprotein (oxLDL). We demonstrate here that the nuclear receptor PPAR gamma is induced in human monocytes following exposure to oxLDL and is expressed at high levels in the foam cells of atherosclerotic lesions. Ligand activation of the PPBR gamma:RXR alpha heterodimer in myelomonocytic cell lines induces changes characteristic of monocytic differentiation and promotes uptake of oxLDL through transcriptional induction of the scavenger receptor CD36. These results reveal a novel signaling pathway controlling differentiation and lipid metabolism in monocytic cells, and suggest that endogenous PPAR gamma ligands may be important regulators of gene expression during atherogenesis.
引用
收藏
页码:241 / 252
页数:12
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