Tudge C C, Grellier P, Justine J L
Zoology Department, University of Queensland, Australia.
Mol Reprod Dev. 1994 Jun;38(2):178-86. doi: 10.1002/mrd.1080380209.
The cytoskeletal protein actin was identified in the mature spermatozoon of the European edible crab, Cancer pagurus Linnaeus, by indirect immunofluorescence with monoclonal and polyclonal anti-actin antibodies, fluorescent phalloidin, and DNAase I. The actin was localized in two distinct concentric rings within the acrosome vesicle of the spermatozoon and appeared to correlate with the internal zonation of the vesicle. Modifications of the fluorescent pattern for actin were observed in sperm cells which were undergoing changes associated with the acrosome reaction. In these cases, fluorescent staining was observed in the nucleocytoplasm immediately subjacent to the perforatorial column and sometimes in the perforatorial column within the acrosome vesicle. Equally intense fluorescence was observed in an apical perforatorial projection. SDS-PAGE of C. pagurus sperm confirmed the presence of actin in the cells. A single band of actin (approximately 43 kDa) comigrated with rabbit muscle actin when immunoblotted onto nitrocellulose with mouse monoclonal anti-actin. The actin-associated cytoskeletal proteins alpha-actinin, tropomyosin, and spectrin were also identified within the spermatozoon of C. pagurus using specific polyclonal antibodies, but their presence was not confirmed by SDS-PAGE and immunoblotting.
通过使用单克隆和多克隆抗肌动蛋白抗体、荧光鬼笔环肽和脱氧核糖核酸酶I进行间接免疫荧光法,在欧洲食用蟹(Cancer pagurus Linnaeus)的成熟精子中鉴定出细胞骨架蛋白肌动蛋白。肌动蛋白定位于精子顶体囊泡内两个不同的同心环中,并且似乎与囊泡的内部区域划分相关。在经历与顶体反应相关变化的精子细胞中观察到肌动蛋白荧光模式的改变。在这些情况下,在紧邻穿孔柱下方的核细胞质中观察到荧光染色,有时在顶体囊泡内的穿孔柱中也观察到。在顶端穿孔突出物中观察到同样强烈的荧光。对欧洲食用蟹精子进行十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)证实细胞中存在肌动蛋白。当用小鼠单克隆抗肌动蛋白抗体免疫印迹到硝酸纤维素膜上时,一条肌动蛋白条带(约43 kDa)与兔肌肉肌动蛋白迁移位置相同。还使用特异性多克隆抗体在欧洲食用蟹精子中鉴定出与肌动蛋白相关的细胞骨架蛋白α-辅肌动蛋白、原肌球蛋白和血影蛋白,但SDS-PAGE和免疫印迹未证实它们的存在。