Bisphenol A induces apoptosis and G2-to-M arrest of ovarian granulosa cells

被引:142
|
作者
Xu, JP
Osuga, Y
Yano, T
Morita, Y
Tang, XH
Fujiwara, T
Takai, Y
Matsumi, H
Koga, K
Taketani, Y
Tsutsumi, O
机构
[1] Univ Tokyo, Fac Med, Dept Obstet & Gynecol, Bunkyo Ku, Tokyo 1138655, Japan
[2] Japan Sci & Technol, CREST, Kawaguchi, Saitama 3320012, Japan
基金
日本学术振兴会;
关键词
bisphenol A; granulosa cell; apoptosis; G2-to-M arrest; Bax; Bcl2;
D O I
10.1006/bbrc.2002.6644
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
We investigated the impact of bisphenol A (BPA) on murine ovarian granulosa cells. Ovarian granulosa cells were cultured with 100 fM to 100 muM BPA for 24 h to 72 h. BPA decreased granulosa cell viability in a dose- and time-dependent manner. The lowest concentration that induced a significant decrease was 100 pM (89.2 +/- 4.0% of the control). TUNEL analysis demonstrated that treatment with BPA increased apoptosis of granulosa cells in a dose- and time-dependent manner. In addition, flow cytometry analyses revealed that treatment with BPA resulted in G2-to-M arrest, which was most prominent at 48 h. BPA increased the expression of Bax and concomitantly decreased the expression of Bc12 at both protein and mRNA levels of granulosa cells. These findings suggest that low, presumably environmentally relevant doses of BPA, decrease the viability of granulosa cells by inducing apoptosis and G2-to-M arrest. Up-regulation of Bax and down-regulation of 1362 were suggested to be involved in this apoptotie effect. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:456 / 462
页数:7
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