Leyton L, Saling P
Department of Obstetrics and Gynecology, Duke University Medical Center, Durham, North Carolina 27710.
J Cell Biol. 1989 Jun;108(6):2163-8. doi: 10.1083/jcb.108.6.2163.
In the mouse, considerable evidence indicates that initial sperm binding to the zona pellucida (ZP) is mediated by ZP3. In addition, this same glycoprotein is also responsible for inducing the acrosome reaction (AR). Whereas the O-linked oligosaccharides of ZP3 appear to mediate sperm-ZP binding, the portion of ZP3 bearing AR activity has not been defined. To try to understand the bifunctional role of ZP3 (binding and AR inducing activities), we have examined the hypothesis that ZP3 aggregates sperm receptor molecules. By analogy with findings in a variety of other extracellular signal transducing systems, including receptors for growth factors and insulin, this aggregation event could initiate the cascade resulting in the AR. To test this hypothesis, we have generated monospecific polyclonal antibodies against ZP2 and against ZP3, and examined the effects of these probes on capacitated sperm incubated in the absence or presence of various ZP protein preparations. For some experiments, we have used proteolytic fragments of ZP3, a preparation known to retain specific binding, but not AR-inducing, activity. We show here that capacitated mouse sperm, incubated with ZP glycopeptides, displayed ARs when incubated subsequently with anti-ZP3 IgG; ARs did not occur when parallel sperm samples were incubated with anti-ZP2 IgG or with anti-ZP3 Fab fragments. When capacitated sperm were treated successively, with (a) ZP3 glycopeptides, (b) anti-ZP3 Fab fragments, and (c) goat anti-rabbit IgG, ARs occurred in the majority of sperm. An alternative approach to examine this hypothesis used ZP proteins obtained from tubal eggs treated previously with bioactive phorbol diester (12-O-tetradecanoyl phorbol-13-acetate [TPA]). This preparation arrests capacitated sperm in an intermediate state of the AR. We demonstrate here that these sperm can be induced to undergo a complete AR by subsequent treatment with anti-ZP3 IgG. Together, these findings are consistent with the hypothesis under examination, and suggest that the aggregation of sperm molecules recognized by ZP3 glycopeptides or by TPA-treated ZP is sufficient to trigger the events that occur during acrosomal exocytosis.
在小鼠中,大量证据表明精子最初与透明带(ZP)的结合是由ZP3介导的。此外,这种相同的糖蛋白还负责诱导顶体反应(AR)。虽然ZP3的O-连接寡糖似乎介导精子与ZP的结合,但具有AR活性的ZP3部分尚未明确。为了试图理解ZP3的双重功能(结合和诱导AR活性),我们检验了ZP3聚集精子受体分子的假说。与包括生长因子和胰岛素受体在内的多种其他细胞外信号转导系统中的发现类似,这种聚集事件可能启动导致AR的级联反应。为了验证这一假说,我们制备了针对ZP2和ZP3的单特异性多克隆抗体,并研究了这些探针在不存在或存在各种ZP蛋白制剂的情况下对获能精子的影响。在一些实验中,我们使用了ZP3的蛋白水解片段,该制剂已知保留特异性结合活性,但不具有诱导AR的活性。我们在此表明,与ZP糖肽一起孵育的获能小鼠精子,随后与抗ZP3 IgG一起孵育时会发生AR;当平行精子样本与抗ZP2 IgG或抗ZP3 Fab片段一起孵育时,不会发生AR。当获能精子依次用(a)ZP3糖肽、(b)抗ZP3 Fab片段和(c)山羊抗兔IgG处理时,大多数精子会发生AR。检验这一假说的另一种方法是使用从先前用生物活性佛波酯(12-O-十四酰佛波醇-13-乙酸酯[TPA])处理过的输卵管卵中获得的ZP蛋白。这种制剂使获能精子停滞在AR的中间状态。我们在此证明,这些精子随后用抗ZP3 IgG处理可被诱导经历完全的AR。总之,这些发现与所检验的假说一致,并表明被ZP3糖肽或经TPA处理的ZP识别的精子分子聚集足以触发顶体胞吐过程中发生的事件。