Queensland Institute of Medical Research, Herston, Queensland, Australia.
Int J Parasitol. 2013 Sep;43(10):785-93. doi: 10.1016/j.ijpara.2013.04.003. Epub 2013 May 20.
The tegument, or body wall, of schistosomes is the primary tissue for host interaction and site targeted schistosome vaccination. However, many aspects of the cell biology, particularly differentiation and maintenance, remain uncharacterised. A leading vaccine candidate, Schistosoma mansoni tetraspanin 2 has proven efficacy in experimental models, but its function, precise subcellular location in the tegument and role in tegument biology is not well understood. A primary question is whether this molecule is a true surface molecule, that is, whether it appears within the apical membrane of the tegument. Hitherto, the target sequence for antibody localisation studies had not been available for advanced subcellular localisation studies, such as immuno-electron microscopy, due to aldehyde sensitivity. To circumvent this problem, we adapted the methods of high pressure freezing and cryosubstitution with uranyl acetate for immuno-electron microscopy. The tri-dimensional structure of tegument membranes was resolved using electron tomography. Immunolocalisation of Schistosoma mansoni tetraspanin 2 demonstrates that the molecule is localised to tegument membrane compartments, but predominantly within internal structures associated with surface invaginations and internal vesicles. Surprisingly, no label was found at the virtual surface of the parasite. The significance of this localisation pattern is discussed.
血吸虫的表皮(或体壁)是宿主相互作用和靶向血吸虫疫苗接种的主要组织。然而,细胞生物学的许多方面,特别是分化和维持,仍然没有得到描述。一种领先的疫苗候选物曼氏血吸虫四跨膜蛋白 2 在实验模型中已被证明有效,但它的功能、在表皮中的精确亚细胞位置及其在表皮生物学中的作用尚不清楚。一个主要问题是,这种分子是否是真正的表面分子,也就是说,它是否出现在表皮的顶膜内。迄今为止,由于醛敏感性,用于抗体定位研究的靶序列尚不适用于免疫电子显微镜等先进的亚细胞定位研究。为了避免这个问题,我们采用了高压冷冻和用铀酰醋酸盐进行低温置换的方法进行免疫电子显微镜研究。使用电子断层摄影术解析了表皮膜的三维结构。曼氏血吸虫四跨膜蛋白 2 的免疫定位表明,该分子定位于表皮膜隔室,但主要位于与表面内陷和内部囊泡相关的内部结构内。令人惊讶的是,在寄生虫的虚拟表面上没有发现标记。讨论了这种定位模式的意义。