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高分辨率电子显微镜观察研究内阿米巴属包囊壁

High-resolution electron microscopical study of cyst walls of Entamoeba spp.

机构信息

Department of Infectomics and Molecular Pathogenesis, Centro de Investigación y de EstudiosAvanzados, Avenue IPN 2508, Zacatenco 07360, Mexico City, Mexico.

出版信息

J Eukaryot Microbiol. 2011 Nov-Dec;58(6):480-6. doi: 10.1111/j.1550-7408.2011.00576.x. Epub 2011 Aug 25.

Abstract

Knowledge of the fine structural organization, molecular composition and permeability properties of the cell surface of intestinal protozoan cysts is important to understand the biologic basis of their resistance. Recent studies on the biology of the cyst walls of Entamoeba histolytica and Entamoeba invadens have considerably advanced knowledge on the cellular processes involved in the transport and surface deposition of the main cyst wall components. Using transmission electron microscopy, cytochemistry, scanning electron microscopy and freeze-fracture techniques, we have obtained new information. In mature cysts the permeability of Entamoeba cysts is limited to small molecules not by the cyst wall, but by the plasma membrane, as demonstrated with the use of ruthenium red as an electron-dense tracer. Cell walls of E. histolytica cysts are made up of five to seven layers of unordered fibrils 7-8 nm thick. Alcian blue stains a regular mesh of fibrils approximately 4 nm thick, running perpendicularly to the cyst wall. In addition, abundant ionogenic groups are seen in cyst walls treated with cationized ferritin. In the mature cysts of E. histolytica and E. invadens small cytoplasmic vesicles with granular material were in close contact with the plasma membrane, suggesting a process of fusion and deposition of granular material to the cell wall. The plasma membrane of mature cysts is devoid of intramembrane particles when analyzed with the freeze-fracture technique. When viewed with scanning electron microscopy the surface of E. histolytica cysts clearly differs from that of Entamoeba coli and E. invadens.

摘要

了解肠道原虫包囊细胞表面的精细结构组织、分子组成和通透性特性对于理解其抗性的生物学基础非常重要。最近对溶组织内阿米巴和侵袭性内阿米巴包囊壁生物学的研究极大地提高了我们对参与主要包囊壁成分运输和表面沉积的细胞过程的认识。通过透射电子显微镜、细胞化学、扫描电子显微镜和冷冻断裂技术,我们获得了新的信息。在成熟的包囊中,电子致密示踪剂钌红的使用表明,内阿米巴包囊的通透性受到限制的不是包囊壁,而是质膜,小分子不能通过。溶组织内阿米巴包囊壁由 5 到 7 层厚约 7-8nm 的无序原纤维组成。阿辛蓝染色显示,与包囊壁垂直的厚约 4nm 的规则原纤维网格。此外,用阳离子化铁蛋白处理的包囊壁中可见大量的离子基团。在成熟的溶组织内阿米巴和侵袭性内阿米巴包囊中,与质膜紧密接触的小细胞质小泡中含有颗粒物质,提示存在颗粒物质融合并沉积到细胞壁的过程。用冷冻断裂技术分析时,成熟包囊的质膜没有内膜颗粒。扫描电子显微镜观察发现,溶组织内阿米巴包囊的表面与大肠杆菌和侵袭性内阿米巴明显不同。

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