Saxena D K, Tanii I, Yoshinaga K, Toshimori K
Department of Anatomy and Reproductive Cell Biology, Miyazaki Medical College, Japan.
J Reprod Fertil. 1999 Sep;117(1):17-25. doi: 10.1530/jrf.0.1170017.
In this study the role of two intra-acrosomal molecules, acrin 1 (MN7) and acrin 2 (MC41), during in vitro fertilization (IVF) was examined. The pertinent monoclonal antibodies mMN7 and mMC41 specifically recognize a 90 kDa protein (acrin 1) localized to the entire acrosome and a 200 kDa protein (acrin 2) localized to the cortex region of the anterior acrosome, respectively. Experiments were designed to assess the effects of mMN7 and mMC41 on fertilization in mice using TYH medium containing mMN7 or mMC41 at 0.0, 0.025, 0.05 and 0.1 mg ml-1. Under these conditions, capacitated spermatozoa inseminated the cumulus-invested oocytes. Acrosome-reacted spermatozoa inseminated the zona pellucida-free oocytes. The antibodies had no effect on sperm motility and primary binding to the zona pellucida, but significantly inhibited the rate of fertilization of zona pellucida-intact oocytes in a dose-dependent manner. A significantly small number of spermatozoa remained attached to the zona pellucida at 5 h after insemination in the presence of mMC41. mMC41 and mMN7 antibodies did not affect the fertilization rate of zona pellucida-free oocytes. Confocal laser scanning microscopy with indirect immunofluorescence traced the effect of the monoclonal antibodies on the zona pellucida-induced acrosome reaction, and revealed that mMN7 prevented completion of acrosomal matrix dispersal, whereas mMC41 did not affect the acrosome reaction. mMC41 appeared to inhibit secondary binding or some biochemical steps on the zona pellucida after the acrosome reaction but before penetration of the zona pellucida. Thus, the intra-acrosomal antigenic molecules acrin 1 and acrin 2 are essential for distinct events before sperm penetration of the zona pellucida in mice.
在本研究中,检测了顶体内的两种分子,即顶体素1(MN7)和顶体素2(MC41)在体外受精(IVF)过程中的作用。相关单克隆抗体mMN7和mMC41分别特异性识别定位于整个顶体的90 kDa蛋白(顶体素1)和定位于顶体前部皮质区域的200 kDa蛋白(顶体素2)。实验旨在评估mMN7和mMC41对小鼠受精的影响,使用含有浓度为0.0、0.025、0.05和0.1 mg/ml的mMN7或mMC41的TYH培养基。在这些条件下,获能精子使有卵丘包裹的卵母细胞受精。顶体反应后的精子使无透明带的卵母细胞受精。这些抗体对精子活力和与透明带的初始结合没有影响,但以剂量依赖的方式显著抑制了完整透明带卵母细胞的受精率。在存在mMC41的情况下,受精后5小时,附着在透明带上的精子数量显著减少。mMC41和mMN7抗体不影响无透明带卵母细胞的受精率。共聚焦激光扫描显微镜结合间接免疫荧光追踪了单克隆抗体对透明带诱导的顶体反应的影响,结果显示mMN7阻止了顶体基质的完全分散,而mMC41不影响顶体反应。mMC41似乎抑制了顶体反应后但在穿透透明带之前在透明带上的二次结合或一些生化步骤。因此,顶体内抗原分子顶体素1和顶体素2对于小鼠精子穿透透明带之前的不同事件至关重要。