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首页> 外文期刊>Molecular human reproduction. >Fas expression correlates with human germ cell degeneration in meiotic and post-meiotic arrest of spermatogenesis.
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Fas expression correlates with human germ cell degeneration in meiotic and post-meiotic arrest of spermatogenesis.

机译:Fas表达与精子发生减数分裂和减数分裂后停滞的人类生殖细胞变性有关。

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摘要

Degeneration of human male germ cells was analysed by means of light (LM) and transmission electron (TEM) microscopy. The frequency of degenerating cells was correlated with that of Fas-expressing germ cells in human testes with normal spermatogenesis (n = 10), complete early maturation arrest (EMA) (n = 10) or incomplete late maturation arrest (LMA; n = 10) of spermatogenesis. LM analysis of testis sections with normal spermatogenesis indicated that degenerating germ cells were localized in the adluminal compartment of the seminiferous epithelium. TEM showed that apoptotic cells were mostly primary spermatocytes and, to a lesser extent, round or early elongating spermatids. Apoptotic germ cells appeared to be eliminated either in the seminiferous lumen or by Sertoli cell phagocytosis. An increased number of degenerating cells was observed in testes with LMA as compared with normal testes and testes with EMA of spermatogenesis (P < 0.001, Wilcoxon's rank sum test). Comparison of these results with those obtained from immunohistochemistry experiments demonstrated a tight correlation between the number of apoptotic cells and the number of Fas-expressing germ cells (P = 0.001, Spearman's rank = 0.69). These findings suggest that altered meiotic and post-meiotic germ cell maturation might be associated with an up-regulation of Fas gene expression capable of triggering apoptotic elimination of defective germ cells.
机译:人类男性生殖细胞的变性通过光(LM)和透射电子(TEM)显微镜进行了分析。在具有正常精子形成(n = 10),完全早期成熟停止(EMA)(n = 10)或不完全晚期成熟停止(LMA; n = 10)的人睾丸中,退化细胞的频率与表达Fas的生殖细胞的频率相关。 )的精子发生。精子发生正常的睾丸切片的LM分析表明,退化的生殖细胞位于生精上皮的腔室中。 TEM显示,凋亡细胞主要是原代精子细胞,程度较小的是圆形或早期伸长的精子细胞。凋亡的生殖细胞似乎在生精管腔或通过支持细胞吞噬作用被消除。与正常睾丸和具有生精EMA的睾丸相比,在LMA睾丸中观察到的变性细胞数量增加(P <0.001,Wilcoxon秩和检验)。将这些结果与从免疫组织化学实验中获得的结果进行比较,结果表明凋亡细胞数量与表达Fas的生殖细胞数量之间存在紧密的相关性(P = 0.001,Spearman等级= 0.69)。这些发现表明减数分裂和减数分裂后生殖细胞成熟的改变可能与Fas基因表达的上调有关,该基因能够触发凋亡消除有缺陷的生殖细胞。

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