Castellani-Ceresa L, Brivio M F, Radaelli G
Department of Biology, University of Milan, Italy.
Mol Reprod Dev. 1992 Sep;33(1):99-107. doi: 10.1002/mrd.1080330114.
Biochemical and immunoelectron microscopic methods have been used to analyze the distribution of actin in boar spermatozoa and its state of aggregation before and after acrosome reaction. F-actin was detected on sperm head and tail by electron microscopy using an improved phalloidin probe: incubation with a fluorescein-phalloidin complex and an anti-fluorescein antibody, followed by labeling with protein A-gold complex. Gold particles, indicating the presence of F-actin, were localized on the sperm surface of the acrosome-reacted spermatozoa. Specific labeling was localized (1) between the outer acrosomal membrane and the plasma membrane in the equatorial region, (2) between the outer surface of the fibrous sheath and the plasma membrane in the postacrosomal region, (3) around the connecting piece and the neck region, and (4) on the external surface of the fibrous sheath in the principal piece of the tail. Furthermore, after NP-40 extraction, the SDS-PAGE revealed a difference in solubility between reacted and unreacted boar spermatozoa, reflecting actin polymerization. We conclude that most actin in the acrosome reacted boar spermatozoa is polymeric.
已采用生化和免疫电子显微镜方法分析了公猪精子中肌动蛋白的分布及其在顶体反应前后的聚集状态。使用改进的鬼笔环肽探针通过电子显微镜在精子头部和尾部检测到F-肌动蛋白:与荧光素-鬼笔环肽复合物和抗荧光素抗体孵育,然后用蛋白A-金复合物标记。表明存在F-肌动蛋白的金颗粒定位于顶体反应精子的精子表面。特异性标记定位于:(1)赤道区顶体外膜与质膜之间;(2)顶体后区纤维鞘外表面与质膜之间;(3)连接段和颈部区域周围;(4)尾部主段纤维鞘外表面。此外,NP-40提取后,SDS-PAGE显示反应和未反应的公猪精子在溶解度上存在差异,反映了肌动蛋白的聚合作用。我们得出结论,顶体反应的公猪精子中大多数肌动蛋白是聚合的。