首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >Immunodetection of aromatase in mice with a partial deletion in the long arm of the Y chromosome.
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Immunodetection of aromatase in mice with a partial deletion in the long arm of the Y chromosome.

机译:免疫检测小鼠Y染色体长臂部分缺失的芳香酶。

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摘要

Aromatization of androgens into estrogens is catalyzed by a microsomal enzyme, P450 aromatase. Males of the mouse strain B10.BR and its congenic mutant strain B10.BR-Ydel (with a partial deletion in the long arm of the Y chromosome) were used to identify the cellular source of estrogens within the testis. Immunocytochemistry was applied to localize aromatase in cultured Leydig cells, cytoplasmic droplets attached to flagella of spermatozoa, and sections of testes. The presence of aromatase in testes was checked by means of Western-blot analysis. Steroid hormones secreted by Leydig cells in vitro were measured in homogenates of testes using radioimmunological methods. Additionally, a Southern analysis was performed using the Y353/B probe to check the length of the deletion in the Y chromosome. In sections of testis of B10.BR mice, weak to moderate immunohistochemical staining of aromatase was found in Leydig cells, Sertoli cells, and germ cells. In testicular cells of B10.BR-Ydel mice, stronger immunostaining of aromatase was observed, especially in germ cells and Leydig cells. Positivity for aromatase was also found in the cytoplasm of cultured Leydig cells from both strains, but it was higher in cells derived from mutant males. Western-blot analysis revealed one major band of approx. 55kDa of aromatase in testes from both strains. Lower testosterone levels were found in mutant males in supernatants of culture media and homogenates of testes in comparison with control males. In contrast, estradiol levels were always higher in mutants. Therefore, it seems likely that the increased expression of aromatase and, as a consequence, the higher levels of endogenous estrogens enhance the morphological alterations in testis and affect spermatogenesis in mutant males.
机译:微粒体酶P450芳香化酶将雄激素芳香化为雌激素。小鼠品系B10.BR及其同系突变体品系B10.BR-Ydel(在Y染色体长臂上部分缺失)的雄性被用于鉴定睾丸内雌激素的细胞来源。免疫细胞化学法用于在培养的Leydig细胞,附着于精子鞭毛的细胞质液滴和睾丸切片中定位芳香化酶。通过蛋白质印迹分析检查睾丸中芳香化酶的存在。使用放射免疫方法在睾丸匀浆中测量Leydig细胞体外分泌的类固醇激素。另外,使用Y353 / B探针进行Southern分析以检查Y染色体中缺失的长度。在B10.BR小鼠的睾丸切片中,在Leydig细胞,Sertoli细胞和生殖细胞中发现了芳香酶的弱至中度免疫组化染色。在B10.BR-Ydel小鼠的睾丸细胞中,观察到更强的芳香化酶免疫染色,特别是在生殖细胞和Leydig细胞中。在两种菌株培养的Leydig细胞的细胞质中也发现了对芳香化酶的正性,但是在源自突变雄性的细胞中,芳香化酶的正性更高。 Western-blot分析显示大约有一个主要谱带。两种菌株的睾丸中的芳香化酶均为55kDa。与对照男性相比,在培养基和睾丸匀浆的上清液中突变男性中睾丸激素水平较低。相反,突变体中的雌二醇水平始终较高。因此,增加的芳香化酶表达以及较高水平的内源性雌激素似乎增强了睾丸的形态变化并影响了突变男性的精子发生。

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