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缺乏丝氨酸蛋白酶抑制剂蛋白酶nexin-1的小鼠的雄性生育缺陷。

Male fertility defects in mice lacking the serine protease inhibitor protease nexin-1.

作者信息

Murer V, Spetz J F, Hengst U, Altrogge L M, de Agostini A, Monard D

机构信息

Friedrich Miescher Institute, Maulbeerstrasse 66, CH 4058 Basel, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3029-33. doi: 10.1073/pnas.051630698. Epub 2001 Feb 27.

Abstract

Understanding infertility and sterility requires knowledge of the molecular mechanisms underlying sexual reproduction. We have found that male mice deficient for the gene encoding the protease inhibitor protease nexin-1 (PN-1) show a marked impairment in fertility from the onset of sexual maturity. Absence of PN-1 results in altered semen protein composition, which leads to inadequate semen coagulation and deficient vaginal plug formation upon copulation. Progressive morphological changes of the seminal vesicles also are observed. Consistent with these findings, abnormal PN-1 expression was found in the semen of men displaying seminal dysfunction. The data demonstrate that the level of extracellular proteolytic activity is a critical element in controlling male fertility.

摘要

了解不育症和不孕需要掌握有性生殖背后的分子机制。我们发现,编码蛋白酶抑制剂蛋白酶nexin-1(PN-1)的基因缺失的雄性小鼠从性成熟开始就表现出明显的生育能力受损。PN-1的缺失导致精液蛋白质组成改变,从而导致精液凝固不足以及交配时阴道栓形成不足。还观察到精囊的渐进性形态变化。与这些发现一致,在显示精液功能障碍的男性精液中发现了异常的PN-1表达。数据表明,细胞外蛋白水解活性水平是控制男性生育能力的关键因素。

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