Bisphenol A diglycidyl ether (BADGE) is a PPARγ agonist in an ECV304 cell line

被引:61
作者
Bishop-Bailey, D
Hla, T
Warner, TD
机构
[1] St Bartholomews & Royal London Sch Med & Dent, William Harvey Res Inst, Dept Cardiac Vasc & Inflammat Res, London EC1M 6BQ, England
[2] Univ Connecticut, Ctr Hlth, Ctr Vasc Biol, Farmington, CT 06030 USA
关键词
PPAR gamma; reporter gene; bisphenol A diglycidyl ether;
D O I
10.1038/sj.bjp.0703628
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Peroxisome proliferator activated receptors (PPAR)s are nuclear transcription factors of the steroid receptor super-family. One member, PPAR gamma, a critical transcription factor in adipogenesis, is expressed in ECV304 cells, and when activated participates in the induction of cell death by apoptosis. Here we describe a clone of ECV304 cells, ECV-ACO.Luc, which stably expresses a reporter gene for PPAR activation. ECV-ACO.Luc respond to the PPAR gamma agonists, 15-deoxy-Delta (12,14) PGJ(2), and ciglitizone, by inducing luciferase expression. Furthermore, using ECV-ACO.Luc, we demonstrate that a newly described PPAR gamma antagonist, bisphenol A diglycidyl ether (BADGE) has agonist activities. Similar to 15-deoxy-Delta (12,14) PGJ(2), BADGE induces PPAR gamma activation, nuclear localization of the receptor, and induces cell death.
引用
收藏
页码:651 / 654
页数:4
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