Storey B T
Department of Obstetrics and Gynecology, University of Pennsylvania Medical Center, Philadelphia 19104-6080, USA.
Reprod Fertil Dev. 1995;7(4):927-42. doi: 10.1071/rd9950927.
Sexual reproduction requires that the gamete carrying the male-derived haploid chromatin join with the gamete carrying the female-derived haploid chromatin during fertilization to produce the diploid zygote. To accomplish this feat, the sperm must not only meet the egg, it must recognize the egg and be recognized in turn by the egg, and in the end must enter and be engulfed by the egg. In this selective overview of gamete interactions that lead to fertilization, encounters of three kinds, followed by the finale of gamete fusion, are considered from the sperm's viewpoint, with particular emphasis on the mammalian species with the mouse as the principal model. The first encounter is with the zona pellucida of the egg, to whose surface the sperm must bind. Mouse sperm appear to have four binding sites for zona ligands. Three interact with sugar moieties of the oligosaccharide chains of the mouse zona glycoprotein ZP3; the fourth binds a peptide backbone arginine. Capacitation is not required for this encounter, but is obligate for the second encounter--induction of the acrosome reaction in the bound sperm. The acrosome reaction is an exocytotic process that makes available the enzymatic machinery needed for sperm penetration the zona which is the end point of a sequence of reactions directed by intracellular signalling systems. In mouse sperm, these systems are presumed to be activated by ligands on ZP3 binding to ligand-specific sperm receptors with consequent aggregation of receptors. No receptor has been identified with certainty, nor have candidates for putative ZP3 ligands been identified. Completion of the acrosome reaction allows the sperm to penetrate the zona and, bind to the egg plasma membrane, thereby completing the third encounter. In the mouse, a 94-kDa protein appears essential for this binding. In the guinea-pig, a sperm plasma membrane protein (formerly PH-30, now fertilin), is a strong candidate for the mediator of the fusion process by which the egg engulfs the sperm. Decondensation of the sperm chromatin reverses the remarkable packing of DNA organized by sperm protamines. Mitochondrial DNA is also engulfed by the egg; the question of whether this DNA makes a small finite, or null, contribution to cytosolic inheritance is still in debate. The puzzles attending these encounters are presented as reminders of the intricacy and fascination, as well as of the vital necessity, of gamete interaction.
有性生殖要求携带雄性来源单倍体染色质的配子在受精过程中与携带雌性来源单倍体染色质的配子结合,以产生二倍体受精卵。为了完成这一壮举,精子不仅要找到卵子,还必须识别卵子并反过来被卵子识别,最终必须进入卵子并被卵子吞噬。在这篇关于导致受精的配子相互作用的选择性综述中,从精子的角度考虑了三种相遇情况,随后是配子融合的终曲,特别强调以小鼠为主要模型的哺乳动物物种。第一次相遇是与卵子的透明带,精子必须结合到其表面。小鼠精子似乎有四个与透明带配体结合的位点。其中三个与小鼠透明带糖蛋白ZP3寡糖链的糖部分相互作用;第四个结合肽主链精氨酸。这次相遇不需要获能,但第二次相遇——诱导结合的精子发生顶体反应——则必须获能。顶体反应是一个胞吐过程,它使精子穿透透明带所需的酶机制得以发挥作用,透明带是由细胞内信号系统引导的一系列反应的终点。在小鼠精子中,这些系统被认为是由ZP3上的配体与配体特异性精子受体结合而激活的,从而导致受体聚集。尚未确定任何受体,也未确定假定的ZP3配体的候选物。顶体反应的完成使精子能够穿透透明带并与卵质膜结合,从而完成第三次相遇。在小鼠中,一种94 kDa的蛋白质似乎对这种结合至关重要。在豚鼠中,一种精子质膜蛋白(以前称为PH - 30,现在称为受精素)是卵子吞噬精子的融合过程的介导物的有力候选者。精子染色质的解聚逆转了由精子鱼精蛋白组织的DNA的显著包装。线粒体DNA也被卵子吞噬;这种DNA对胞质遗传的贡献是微小、有限还是为零,这个问题仍在争论中。这些相遇中存在的谜题提醒人们,配子相互作用既错综复杂又引人入胜,同时也是至关重要的。