Sertoli cell junctional proteins as early targets for different classes of reproductive toxicants

被引:185
作者
Fiorini, C
Tilloy-Ellul, A
Chevalier, S
Charuel, C
Pointis, G
机构
[1] Fac Med, INSERM EMI 00 09, IFR 50, F-06107 Nice 02, France
[2] Pfizer, Mol & Cellular Toxicol Lab, F-37401 Amboise, France
关键词
Sertoli cell toxicants; occludin; ZO-1; N-cadherin; Cx43; in vitro model system;
D O I
10.1016/j.reprotox.2004.01.002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the testis, Sertoli cells establish intercellular junctions that are essential for spermatogenesis. The SerW3 Sertoli cell line displays some features of native Sertoli cells. Western blot and immunotluorescence analyses showed that SerW3 Sertoli cells expressed typical components of tight (occludin and zonula occludens-1), anchoring (N-cadherin) and gap (connexin 43) junctions. Testicular toxicants (DDT, pentachlorophenol, dieldrin, dinitrobenzene, cadmium chloride, cisplatin, gossypol, bisphenol A and tert-octylphenol) affected intercellular junctions by either reducing the amount or inducing aberrant intracellular localization of these membranous proteins. Phosphodiesterase inhibitors (isobutyl methylxantine, rolipram, zaprinast, zardaverine) did not alter junctional-complex component levels but caused a rapid and reversible redistribution of these proteins to the cytoplasmic compartment. The present study showed that occludin, ZO-1, N-cadherin and specifically Cx43 could be early targets for testicular toxicants. The SerW3 cell line therefore appears as a useful in vitro model to evaluate molecules with potential anti-reproductive effects. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:413 / 421
页数:9
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