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哺乳动物受精过程中精卵相互作用的早期步骤。

Early steps of sperm-egg interactions during mammalian fertilization.

作者信息

Barros C, Crosby J A, Moreno R D

机构信息

Faculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago.

出版信息

Cell Biol Int. 1996 Jan;20(1):33-9. doi: 10.1006/cbir.1996.0006.

Abstract

Mammalian eggs are surrounded by two egg coats: the cumulus oophorus and the zona pellucida, which is an extracellular matrix composed of sulfated glycoproteins. The first association of the spermatozoon with the zona pellucida occurs between the zona glycoprotein, ZP3 and sperm receptors, located at the sperm plasma membrane, such as the 95 kDa tyrosine kinase-protein. This association induces the acrosome reaction and exposes the proacrosin/acrosin system. Proacrosin transforms itself, by autoactivation, into the proteolytical active form: acrosin. This is a serine protease that has been shown to be involved in secondary binding of spermatozoa to the zona pellucida and in the penetration of mammalian spermatozoa through it. The zona pellucida is a specific and natural substrate for acrosin and its hydrolysis and fertilization can be inhibited by antiacrosin monoclonal antibodies. Moreover, in in vitro fertilization experiments, trypsin inhibitors significantly inhibits fertilization. The use of the silver-enhanced immunogold technique has allowed immunolocalization of the proacrosin/acrosin system in spermatozoa after the occurrence of the acrosome reaction. This system remains associated to the surface of the inner acrosomal membrane for several hours in human, rabbit and guinea-pig spermatozoa while in the hamster it is rapidly lost. In the hamster, the loss of acrosin parallels the capability of the sperm to cross the zona pellucida. Rabbit perivitelline spermatozoa can fertilize freshly ovulated rabbit eggs and retain acrosin in the equatorial and postacrosomal region. These spermatozoa also show digestion halos on gelatin plates that can be inhibited by trypsin inhibitors. This evidence strongly suggests the involvement of acrosin in sperm penetration through the mammalian zona. Recently it was shown, however, that acrosin would not be essential for fertilization. It is likely, then, that such an important phenomenon in the mammalian reproductive cycle would be ensured though several alternative mechanisms.

摘要

哺乳动物的卵子被两层卵膜所包围

卵丘和透明带,透明带是一种由硫酸化糖蛋白组成的细胞外基质。精子与透明带的首次结合发生在透明带糖蛋白ZP3和位于精子质膜上的精子受体之间,比如95 kDa酪氨酸激酶蛋白。这种结合诱导顶体反应并暴露出前顶体蛋白酶/顶体蛋白酶系统。前顶体蛋白酶通过自身激活转化为蛋白水解活性形式:顶体蛋白酶。这是一种丝氨酸蛋白酶,已被证明参与精子与透明带的二次结合以及哺乳动物精子穿透透明带的过程。透明带是顶体蛋白酶的特异性天然底物,其水解和受精过程可被抗顶体蛋白酶单克隆抗体抑制。此外,在体外受精实验中,胰蛋白酶抑制剂能显著抑制受精。银增强免疫金技术已可在顶体反应发生后对精子中的前顶体蛋白酶/顶体蛋白酶系统进行免疫定位。在人类、兔子和豚鼠的精子中,该系统在顶体内膜表面保持数小时,而在仓鼠精子中则迅速消失。在仓鼠中,顶体蛋白酶的消失与精子穿过透明带的能力平行。兔卵周精子可使刚排卵的兔卵受精,并在赤道区和顶体后区保留顶体蛋白酶。这些精子在明胶平板上也显示出消化晕,可被胰蛋白酶抑制剂抑制。这些证据有力地表明顶体蛋白酶参与了精子穿透哺乳动物透明带的过程。然而,最近研究表明,顶体蛋白酶对受精并非必不可少。那么,哺乳动物生殖周期中的这一重要现象很可能是通过几种替代机制来确保的。

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