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有证据表明精子金属内蛋白酶活性在人类精子穿透去透明带仓鼠卵过程中发挥作用。

Evidence suggesting a role for sperm metalloendoprotease activity in penetration of zona-free hamster eggs by human sperm.

作者信息

Díaz-Pérez E, Thomas P, Meizel S

机构信息

Department of Human Anatomy, School of Medicine, University of California, Davis 95616.

出版信息

J Exp Zool. 1988 Nov;248(2):213-21. doi: 10.1002/jez.1402480213.

Abstract

It has been reported that metalloendoprotease (MEP) activity is involved in somatic cell membrane fusion events and in the sea urchin sperm acrosome reaction (AR). MEP activity also has been demonstrated in human and other mammalian sperm. The present study was concerned with investigating whether a human sperm MEP is important in membrane events necessary for sperm egg fusion. Ejaculated human sperm were washed, capacitated in vitro, and preincubated with the competitive MEP inhibitors phosphoramidon (50 microM) or CBZ-L-phenylalanine (1 mM), with 100 microM diethylenetriaminepentaacetic acid (DTPA), a heavy metal chelator, or as controls, with the appropriate solvents. The AR was initiated in vitro with preovulatory human follicular fluid and the sperm washed to dilute inhibitors and then coincubated with zona-free golden hamster eggs (zonae and cumuli removed with trypsin and hyaluronidase, respectively). Eggs were washed after 0.5 h, and the number of sperm remaining bound was counted. After 2.5 h further incubation, the eggs were stained with acetolacmoid or acetoorcein and penetration was assayed by counting the number of decondensed sperm heads per egg (penetration index) and the percent of penetrated eggs. The inhibitor treatments did not decrease the percentage of penetrated eggs (range 80-90%), but a significant reduction in the penetration index was observed. Phosphoramidon reduced the penetration index by 45%, CBZ-L-phenylalanine by 57%, and DTPA by 56%. None of the inhibitors decreased the penetration index or the percentage of penetrated eggs when added directly to suspensions of acrosome-reacted sperm and zona-free eggs at the diluted levels that would have been present after washing inhibitor-treated sperm.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

据报道,金属内蛋白酶(MEP)活性参与体细胞细胞膜融合事件以及海胆精子顶体反应(AR)。在人类和其他哺乳动物精子中也已证实存在MEP活性。本研究旨在调查人类精子MEP在精卵融合所需的膜事件中是否重要。采集射出的人类精子,进行洗涤、体外获能,然后分别与竞争性MEP抑制剂磷酰胺素(50微摩尔)或CBZ-L-苯丙氨酸(1毫摩尔)、重金属螯合剂100微摩尔二乙烯三胺五乙酸(DTPA)预孵育,或作为对照与相应溶剂预孵育。用排卵前的人类卵泡液在体外引发AR,然后洗涤精子以稀释抑制剂,再与去透明带金黄仓鼠卵(透明带和卵丘分别用胰蛋白酶和透明质酸酶去除)共同孵育。0.5小时后洗涤卵子,计算剩余结合的精子数量。进一步孵育2.5小时后,用醋酸洋红或醋酸地衣红对卵子进行染色,通过计算每个卵子中解聚的精子头部数量(穿透指数)和穿透卵子的百分比来测定穿透情况。抑制剂处理并未降低穿透卵子的百分比(范围为80 - 90%),但观察到穿透指数显著降低。磷酰胺素使穿透指数降低了45%,CBZ-L-苯丙氨酸降低了57%,DTPA降低了56%。当以洗涤抑制剂处理后的精子后应有的稀释水平直接添加到顶体反应精子和去透明带卵子的悬浮液中时,没有一种抑制剂会降低穿透指数或穿透卵子的百分比。(摘要截短于250字)

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