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哺乳动物受精:精子蛋白56的奇特案例。

Mammalian fertilization: the strange case of sperm protein 56.

作者信息

Wassarman Paul M

机构信息

Department of Developmental and Regenerative Biology, Mount Sinai School of Medicine, One Gustave L Levy Place, New York, NY 10029-6574, USA.

出版信息

Bioessays. 2009 Feb;31(2):153-8. doi: 10.1002/bies.200800152.

Abstract

During mammalian fertilization sperm bind to the egg's zona pellucida (ZP) after undergoing capacitation. Capacitated mouse sperm bind to mZP3 (one of three ZP glycoproteins), undergo the acrosome reaction, penetrate the ZP, and fuse with egg plasma membrane. Sperm protein 56 (sp56), a member of the C3/C4 superfamily of binding proteins, was identified nearly 20 years ago as a binding partner for mZP3 by photoaffinity cross-linking of acrosome-intact sperm. However, subsequent research revealed that sp56 is a component of the sperm's acrosomal matrix and, for sperm with an intact acrosome, should be unavailable for binding to mZP3. Recently, this dilemma was resolved when it was recognized that some acrosomal matrix (AM) proteins, including sp56, are released to the sperm surface during capacitation. This may explain why uncapacitated mammalian sperm are unable to bind to the unfertilized egg ZP.

摘要

在哺乳动物受精过程中,精子在获能后会与卵子的透明带(ZP)结合。获能的小鼠精子与mZP3(三种ZP糖蛋白之一)结合,发生顶体反应,穿透透明带,并与卵质膜融合。精子蛋白56(sp56)是结合蛋白C3/C4超家族的成员,近20年前通过对顶体完整的精子进行光亲和交联,被鉴定为mZP3的结合伴侣。然而,随后的研究表明,sp56是精子顶体基质的一个组成部分,对于顶体完整的精子来说,应该无法与mZP3结合。最近,当人们认识到一些顶体基质(AM)蛋白,包括sp56,在获能过程中会释放到精子表面时,这个难题得到了解决。这或许可以解释为什么未获能的哺乳动物精子无法与未受精的卵子透明带结合。

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