Boerke A, Tsai P S, Garcia-Gil N, Brewis I A, Gadella B M
Department of Biochemistr, Utrecht University, Yalelaan 2, 3584 CM Utrecht, The Netherlands.
Theriogenology. 2008 Nov;70(8):1188-96. doi: 10.1016/j.theriogenology.2008.06.021. Epub 2008 Jul 21.
For sperm to successfully fertilize an oocyte, it needs to pass through certain steps prior to, during and after initial recognition of the zona pellucida (ZP). During capacitation, the surface of the sperm head becomes remodelled, priming it to bind to the ZP and subsequently to undergo the ZP-induced acrosome reaction. During capacitation, sperm ZP-binding proteins are ordered in functional protein complexes that only emerge at the apical tip of the sperm head plasma membrane; this is also functionally the exclusive sperm surface area involved in primary ZP binding. After primary ZP binding, the same area is probably involved in the induction of the acrosome reaction. A combination of biochemical and proteomic membrane protein techniques have enabled us to dissect and highly purify the apical sperm plasma membrane area from control and capacitated sperm cells. The actual ZP-binding proteins identified predominantly belonged to the sperm membrane-associated family members of spermadhesins (AQN-3) and were present in the aggregating lipid ordered membrane microdomains (lipid rafts) that emerged during in vitro capacitation in the apical ridge area of the sperm head plasma membrane. This clustering of these rafts was dependent on the presence of bicarbonate (involved in protein kinase A activation) and on the presence of albumin (involved in cholesterol removal). Remarkably, cholesterol removal was restricted to the non-raft membrane fraction of the sperm plasma membrane, but did not cause any depletion of cholesterol in the raft membrane fraction. Interestingly, sperm SNARE proteins (both VAMP from the outer acrosomal membrane, as well syntaxin from the apical sperm head plasma membrane) shared lateral redistribution properties, along with the ZP-binding protein complex and raft marker proteins. All of these were recovered after capacitation in detergent-resistant membrane preparations from sperm thought to represent membrane lipid rafts. We inferred that the capacitation-dependent formation of an aggregated lipid ordered apical ridge surface area in the sperm head plasma membrane was not only relevant for ZP-binding, but also for the ZP-induced acrosome reaction.
精子要成功使卵母细胞受精,在最初识别透明带(ZP)之前、期间和之后需要经历某些步骤。在获能过程中,精子头部表面会发生重塑,使其能够与ZP结合,并随后引发ZP诱导的顶体反应。在获能过程中,精子ZP结合蛋白会有序排列成功能性蛋白复合物,这些复合物仅出现在精子头部质膜的顶端;这在功能上也是精子表面唯一参与初级ZP结合的区域。初级ZP结合后,同一区域可能参与顶体反应的诱导。生物化学和蛋白质组学膜蛋白技术的结合使我们能够从对照和获能的精子细胞中分离并高度纯化精子头部顶端质膜区域。鉴定出的实际ZP结合蛋白主要属于精子黏附素(AQN-3)的精子膜相关家族成员,并存在于精子头部质膜顶端嵴区域体外获能过程中出现的聚集性脂质有序膜微区(脂筏)中。这些脂筏的聚集依赖于碳酸氢盐(参与蛋白激酶A激活)的存在和白蛋白(参与胆固醇清除)的存在。值得注意的是,胆固醇的清除仅限于精子质膜的非脂筏膜部分,但并未导致脂筏膜部分的胆固醇有任何消耗。有趣的是,精子SNARE蛋白(来自顶体外膜的VAMP以及来自精子头部顶端质膜的 syntaxin)与ZP结合蛋白复合物和脂筏标记蛋白具有相同的侧向重新分布特性。在认为代表膜脂筏的精子去污剂抗性膜制剂中获能后,所有这些都被回收。我们推断,精子头部质膜中依赖获能形成的聚集性脂质有序顶端嵴表面积不仅与ZP结合有关,而且与ZP诱导的顶体反应有关。