Baibakov Boris, Gauthier Lyn, Talbot Prue, Rankin Tracy L, Dean Jurrien
Laboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD 20892, USA.
Development. 2007 Mar;134(5):933-43. doi: 10.1242/dev.02752.
At fertilization, spermatozoa bind to the zona pellucida (ZP1, ZP2, ZP3) surrounding ovulated mouse eggs, undergo acrosome exocytosis and penetrate the zona matrix before gamete fusion. Following fertilization, ZP2 is proteolytically cleaved and sperm no longer bind to embryos. We assessed Acr3-EGFP sperm binding to wild-type and huZP2 rescue eggs in which human ZP2 replaces mouse ZP2 but remains uncleaved after fertilization. The observed de novo binding of Acr3-EGFP sperm to embryos derived from huZP2 rescue mice supports a ;zona scaffold' model of sperm-egg recognition in which intact ZP2 dictates a three-dimensional structure supportive of sperm binding, independent of fertilization and cortical granule exocytosis. Surprisingly, the acrosomes of the bound sperm remain intact for at least 24 hours in the presence of uncleaved human ZP2 regardless of whether sperm are added before or after fertilization. The persistence of intact acrosomes indicates that sperm binding to the zona pellucida is not sufficient to induce acrosome exocytosis. A filter penetration assay suggests an alternative mechanism in which penetration into the zona matrix initiates a mechanosensory signal transduction necessary to trigger the acrosome reaction.
在受精过程中,精子与排卵后小鼠卵子周围的透明带(ZP1、ZP2、ZP3)结合,发生顶体胞吐作用,并在配子融合前穿透透明带基质。受精后,ZP2被蛋白水解切割,精子不再与胚胎结合。我们评估了Acr3-EGFP精子与野生型和huZP2拯救卵的结合情况,在huZP2拯救卵中,人类ZP2取代了小鼠ZP2,但受精后仍未被切割。观察到Acr3-EGFP精子与huZP2拯救小鼠来源的胚胎发生新生结合,这支持了一种精子-卵子识别的“透明带支架”模型,即完整的ZP2决定了支持精子结合的三维结构,与受精和皮质颗粒胞吐作用无关。令人惊讶的是,在存在未切割的人类ZP2的情况下,无论精子是在受精前还是受精后添加,结合精子的顶体至少24小时保持完整。完整顶体的持续存在表明精子与透明带的结合不足以诱导顶体胞吐作用。一种滤膜穿透试验提示了一种替代机制,即穿透进入透明带基质会启动触发顶体反应所需的机械感觉信号转导。