A PROSTAGLANDIN J(2) METABOLITE BINDS PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA AND PROMOTES ADIPOCYTE DIFFERENTIATION

被引:1825
作者
KLIEWER, SA
LENHARD, JM
WILLSON, TM
PATEL, I
MORRIS, DC
LEHMANN, JM
机构
[1] GLAXO INC,RES INST,DEPT MED CHEM,RES TRIANGLE PK,NC 27709
[2] GLAXO INC,RES INST,DEPT BIOL MOLEC,RES TRIANGLE PK,NC 27709
[3] GLAXO INC,RES INST,DEPT MOLEC PHARMACOL,RES TRIANGLE PK,NC 27709
关键词
D O I
10.1016/0092-8674(95)90194-9
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
Prostaglandins (PGs) of the J(2) series form in vivo and exert effects on a variety of biological processes. While most PGs mediate their effects through G protein-coupled receptors, the mechanism of action for the J(2) series of PGs remains unclear. Here, we report that PGJ(2) and its derivatives are efficacious activators of peroxisome proliferator-activated receptors alpha and gamma (PPAR alpha and PPAR gamma, respectively), orphan nuclear receptors implicated in lipid homeostasis and adipocyte differentiation. The PGJ(2) metabolite 15-deoxy-Delta(12,14)-PGJ(2) binds directly to PPAR gamma and promotes efficient differentiation of C3H10T1/2 fibroblasts to adipocytes. These data provide strong evidence that a fatty acid metabolite can function as an adipogenic agent through direct interactions with PPAR gamma and, furthermore, suggest a novel mechanism of action for PGs of the J(2) series.
引用
收藏
页码:813 / 819
页数:7
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