Ensslin Michael A, Lyng Robert, Raymond Adam, Copland Susannah, Shur Barry D
Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Soc Reprod Fertil Suppl. 2007;63:367-83.
Mammalian fertilization is initiated by species-specific binding of the sperm to the zona pellucida, or egg coat. Previous studies suggested that sperm adhesion to the egg coat is facilitated, at least in part, through the binding of sperm surface beta1 ,4-galactosyltransferase I (GaIT) to glycoside chains on the egg coat glycoprotein, ZP3. Binding of multiple ZP3 oligosaccharides induces aggregation of GaIT within the sperm membrane, triggering, directly or indirectly, a pertussis toxin sensitive G-protein cascade leading to induction of the acrosome reaction. Consistent with this, spermatozoa bearing targeted deletions in GaIT are unable to bind ZP3 or undergo ZP3-dependent acrosomal exocytosis; however, unexpectedly, GaIT-null sperm are still able to bind to the egg coat. This indicates that sperm-egg binding requires at least two independent binding mechanisms; a GaIT-ZP3-independent event that mediates initial adhesion, followed by a GaIT-ZP3 interaction that facilitates acrosomal exocytosis. Our recent efforts have focused on the identification and characterization of these novel gamete receptors. One recently identified sperm protein that is required for sperm adhesion to the egg coat is SED1. SED1 is a bimotif protein composed of two Notch-like EGF repeats and two discoidin/complement F5/8 domains. SED1 is secreted by the epididymal epithelium and coats spermatozoa as they progress through the epididymis. Spermatozoa null for SED1 fail to bind the egg coat, illustrating its requirement for gamete adhesion. Interestingly, SED1 is also expressed by a variety of other epithelial tissues, where it appears to be required for epithelial morphogenesis and/or maintenance. A second novel gamete receptor has recently been identified on the coat of ovulated oocytes. This ZP3-independent, egg coat component is a high molecular weight, wheat germ agglutinin (WGA)-reactive glycoprotein that is derived from oviduct secretions and appears to participate in initial sperm adhesion. The amino acid sequence of this oviduct-derived ligand is currently being determined for the generation of peptide-specific antibodies and for the creation of knock out mice. The identification of novel gamete receptors that are required for sperm-egg binding opens up new avenues for the development of specific contraceptive strategies.
哺乳动物受精始于精子与透明带(即卵膜)的物种特异性结合。先前的研究表明,精子与卵膜的黏附至少部分是通过精子表面的β1,4 - 半乳糖基转移酶I(GaIT)与卵膜糖蛋白ZP3上的糖苷链结合来实现的。多个ZP3寡糖的结合会诱导GaIT在精子膜内聚集,直接或间接触发百日咳毒素敏感的G蛋白级联反应,从而引发顶体反应。与此一致的是,在GaIT中存在靶向缺失的精子无法结合ZP3或进行依赖于ZP3的顶体胞吐作用;然而,出乎意料的是,缺乏GaIT的精子仍然能够与卵膜结合。这表明精子与卵子的结合至少需要两种独立的结合机制:一种不依赖于GaIT - ZP3的事件介导初始黏附,随后是促进顶体胞吐作用的GaIT - ZP3相互作用。我们最近的工作重点是鉴定和表征这些新型配子受体。一种最近鉴定出的精子黏附于卵膜所需的蛋白质是SED1。SED1是一种双基序蛋白,由两个Notch样表皮生长因子重复序列和两个盘状结构域/补体F5/8结构域组成。SED1由附睾上皮分泌,并在精子通过附睾时覆盖精子。缺乏SED1的精子无法结合卵膜,说明了其对配子黏附的必要性。有趣的是,SED1也在多种其他上皮组织中表达,在这些组织中它似乎是上皮形态发生和/或维持所必需的。最近在排卵后的卵母细胞表面鉴定出了第二种新型配子受体。这种不依赖于ZP3的卵膜成分是一种高分子量、与麦胚凝集素(WGA)反应的糖蛋白,它来源于输卵管分泌物,似乎参与了精子的初始黏附。目前正在确定这种来源于输卵管的配体的氨基酸序列,以制备肽特异性抗体并创建基因敲除小鼠。鉴定出精子与卵子结合所需的新型配子受体为开发特定的避孕策略开辟了新途径。