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首页> 外文期刊>International Journal for Parasitology >Tetraspanin-2 localisation in high pressure frozen and freeze-substituted Schistosoma mansoni adult males reveals its distribution in membranes of tegumentary vesicles
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Tetraspanin-2 localisation in high pressure frozen and freeze-substituted Schistosoma mansoni adult males reveals its distribution in membranes of tegumentary vesicles

机译:Tespansin-2在高压冷冻和冷冻取代的曼氏血吸虫成年雄性中的定位显示其在外皮囊泡膜中的分布

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摘要

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.
机译:血吸虫的外皮或体壁是宿主相互作用和定点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,仍未表征。领先的候选疫苗曼氏血吸虫四跨膜蛋白2在实验模型中已证明有效,但其功能,在被膜中的精确亚细胞定位以及在被膜生物学中的作用尚不十分清楚。一个主要的问题是该分子是否为真正的表面分子,即它是否出现在外皮的顶膜内。迄今为止,由于醛敏感性,用于抗体定位研究的靶序列尚未用于高级亚细胞定位研究,例如免疫电子显微镜。为了解决这个问题,我们采用了乙酸铀酰进行高压冷冻和冷冻替代的方法,用于免疫电子显微镜检查。使用电子断层扫描技术解析了被膜的三维结构。曼氏血吸虫四跨膜蛋白2的免疫定位表明该分子定位在被膜隔间,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未发现任何标记。讨论了这种本地化模式的重要性。

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