Ricci M, Breed W G
Department of Anatomical Sciences, The University of Adelaide, South Australia, 5005, Australia.
Reproduction. 2001 Mar;121(3):373-88. doi: 10.1530/rep.0.1210373.
The flagellum of a mammalian spermatozoon consists of a central axoneme surrounded by two cytoskeletal structures, the outer dense fibres and the fibrous sheath, which may aid in sperm motility or stability. In this study the outer dense fibres and fibrous sheath were isolated and partially characterized in a marsupial species, the brushtail possum (Trichosurus vulpecula). Spermatozoa from the cauda epididymidis were decapitated by sonication, and the head and tail fractions were separated by centrifugation over a 20, 40 and 60% (w/v) sucrose density gradient. After confirming sperm tail purity by Nomarski microscopy, the tails were incubated in either SDS-dithiothreitol to isolate the outer dense fibres or urea-dithiothreitol to isolate the fibrous sheaths. Purified outer dense fibres and fibrous sheaths were solubilized in SDS and beta-mercaptoethanol and proteins were separated by one-dimensional PAGE. Coomassie blue staining showed that the outer dense fibres were composed of seven major proteins (molecular masses: 73, 58, 55, 54, 52, 41 and 16 kDa), and the fibrous sheath was composed of 12 major proteins (molecular masses: 106, 76, 66, 62, 55, 53, 52, 46, 40, 30, 28 and 16 kDa). A polyclonal antibody to the fibrous sheath proteins showed strong crossreactivity with those of fibrous sheath from spermatozoa of several other marsupial species, as well as those from laboratory rats. Subsequent western blotting identified the immunoreactive 76 and 62 kDa proteins from all species, thus indicating their high conservation between species. No crossreactivity of the fibrous sheath antibody to any other cytoskeletal structures, including the outer dense fibres, mid-piece fibre network or connecting laminae, or to the acrosome or underlying subacrosomal material, was evident, indicating that the fibrous sheath proteins are localized to this structure alone. Further work is in progress to determine the extent of homology of these proteins to those in eutherian mammals.
哺乳动物精子的鞭毛由中央轴丝以及围绕其的两种细胞骨架结构组成,即外致密纤维和纤维鞘,它们可能有助于精子的运动或稳定性。在本研究中,对有袋类动物帚尾袋貂(Trichosurus vulpecula)的外致密纤维和纤维鞘进行了分离并部分表征。附睾尾部的精子通过超声处理断头,然后通过在20%、40%和60%(w/v)蔗糖密度梯度上离心,将头部和尾部组分分离。通过Nomarski显微镜确认精子尾部纯度后,将尾部在SDS-二硫苏糖醇中孵育以分离外致密纤维,或在尿素-二硫苏糖醇中孵育以分离纤维鞘。纯化的外致密纤维和纤维鞘在SDS和β-巯基乙醇中溶解,蛋白质通过一维PAGE分离。考马斯亮蓝染色显示,外致密纤维由七种主要蛋白质组成(分子量分别为:73、58、55、54、52、41和16 kDa),纤维鞘由12种主要蛋白质组成(分子量分别为:106、76、66、62、55、53、52、46、40、30、28和16 kDa)。一种针对纤维鞘蛋白的多克隆抗体与其他几种有袋类动物精子以及实验室大鼠精子的纤维鞘蛋白表现出强烈的交叉反应性。随后的蛋白质印迹法鉴定出所有物种中具有免疫反应性的76 kDa和62 kDa蛋白质,这表明它们在物种间具有高度保守性。纤维鞘抗体与任何其他细胞骨架结构,包括外致密纤维、中段纤维网络或连接片层,或与顶体或其下方的顶体下物质均无明显交叉反应,这表明纤维鞘蛋白仅定位于该结构。进一步的工作正在进行中,以确定这些蛋白质与真兽类哺乳动物中蛋白质的同源程度。