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首页> 外文期刊>Archives of Andrology: An International Journal >Expression of bcl-2 and bax in rhesus monkey testis during germ cell apoptosis induced by testosterone undecanoate.
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Expression of bcl-2 and bax in rhesus monkey testis during germ cell apoptosis induced by testosterone undecanoate.

机译:十一酸睾丸酮诱导生殖细胞凋亡期间恒河猴睾丸bcl-2和bax的表达。

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摘要

Apoptosis occurs spontaneously during spermatogenesis and can be induced by androgen withdrawal. However, the molecular events governing apoptosis have not been characterized. To study the molecular mechanism of apoptosis induced by a high dose of testosterone undecanoate (TU), the authors examined the temporal changes in proapoptotic Bax and antiapoptotic Bcl-2 in TU-treated monkey testes. Apoptotic cells were identified in tissue sections by in situ end labeling of fragmented DNA. The results showed that a great deal of the apoptotic cells occurred in the testes on day 30 after TU injection and that the dominant apoptotic germ cells are spermatocytes and spermatids. The expression of Bcl-2 and Bax was assessed by immunohistochemical method and Western blot. As compared with that of normal testes, the levels of Bcl-2 protein increased significantly from 7 to day 14 while that of Bax protein was almost unchanged in the testes from day 7 up to day 60 after TU treatment. Bcl-2 was localized to the spermatids in the normal testes and temporarily distributed in both the cytoplasm and nucleus of those cell types susceptible to TU-induced apoptosis on day 14 after TU injection. Therefore, it is suggested that Bax may not play a role in initiating germ cell apoptosis induced by TU injection and that the evaluation in Bcl-2 expression may represent a survival mechanism for the remaining germ cell.
机译:细胞凋亡在精子发生过程中自发发生,可以由雄激素戒断引起。但是,尚无控制凋亡的分子事件。为了研究高剂量十一酸睾丸激素(TU)诱导的细胞凋亡的分子机制,作者研究了TU处理的猴睾丸中促凋亡Bax和抗凋亡Bcl-2的时间变化。通过片段化DNA的原位末端标记在组织切片中鉴定出凋亡细胞。结果表明,TU注射后第30天,睾丸中出现大量凋亡细胞,主要的凋亡生殖细胞是精细胞和精细胞。通过免疫组织化学和Western blot检测Bcl-2和Bax的表达。与正常睾丸相比,TU处理后从第7天到第60天,Bcl-2蛋白的水平从第7天到第14天显着增加,而Bax蛋白的水平几乎没有变化。 Bcl-2定位于正常睾丸中的精子,并在TU注射后第14天暂时分布在那些易受TU诱导的细胞凋亡的细胞类型的细胞质和细胞核中。因此,提示Bax可能在由TU注射诱导的生殖细胞凋亡的启动中不起作用,并且对Bcl-2表达的评估可能代表了剩余生殖细胞的存活机制。

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