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雄性生殖细胞中雄激素依赖的细胞凋亡是通过原癌蛋白Cbl来调节的。

Androgen-dependent apoptosis in male germ cells is regulated through the proto-oncoprotein Cbl.

作者信息

El Chami Nisrine, Ikhlef Fouziha, Kaszas Krisztian, Yakoub Sadok, Tabone Eric, Siddeek Benazir, Cunha Stéphanie, Beaudoin Claude, Morel Laurent, Benahmed Mohamed, Régnier Daniel C

机构信息

Faculté de Médecine Lyon-Sud, Institut National de la Santé et la Recherche Médicale, F-69921 Oullins Cedex, France.

出版信息

J Cell Biol. 2005 Nov 21;171(4):651-61. doi: 10.1083/jcb.200507076.

Abstract

The proto-oncoprotein Cbl is known to control several signaling processes. It is highly expressed in the testis, and because spermatogenesis is androgen dependent, we investigated the androgen dependency expression of Cbl through its testicular sub-localization and its expression levels in rats that were exposed to the antiandrogen flutamide or were hypophysectomized. We report the androgen dependency of Cbl as it localizes in pachytene spermatocytes during androgen-dependent stages, is down-regulated upon flutamide exposure, and is up-regulated with testosterone in hypophysectomized rats. Coculture experiments showed the key control exerted by the Sertoli cell on Cbl activity. As flutamide induces germ cell apoptosis, we investigate members of the Bcl-2 family upon flutamide exposure. We show that the proapoptotic Bcl-2 family member Bim mirrored Cbl expression through a posttranscriptional process. We also show that in Cbl knockout mouse testes, the imbalance between the high expression of Bim and Smac/Diablo and anti-apoptotic factors such as cellular inhibitor of apoptosis 2 favors a survival process, which makes these mice unresponsive to androgen withdrawal and could explain their hypofertility.

摘要

原癌蛋白Cbl已知可控制多种信号传导过程。它在睾丸中高度表达,由于精子发生依赖雄激素,我们通过其在睾丸中的亚定位及其在暴露于抗雄激素氟他胺或垂体切除的大鼠中的表达水平,研究了Cbl的雄激素依赖性表达。我们报告了Cbl的雄激素依赖性,因为它在雄激素依赖阶段定位于粗线期精母细胞,在氟他胺暴露后下调,在垂体切除的大鼠中随睾酮上调。共培养实验显示了支持细胞对Cbl活性的关键控制作用。由于氟他胺诱导生殖细胞凋亡,我们研究了氟他胺暴露后Bcl-2家族成员的情况。我们发现促凋亡的Bcl-2家族成员Bim通过转录后过程反映了Cbl的表达。我们还表明,在Cbl基因敲除小鼠的睾丸中,Bim和Smac/Diablo的高表达与抗凋亡因子如细胞凋亡抑制因子2之间的失衡有利于生存过程,这使得这些小鼠对雄激素撤退无反应,并可以解释它们的生育力低下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f5a/2171555/e457aa0a9120/200507076f1.jpg

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