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扫描显微镜的新进展及其在研究寄生原生动物中的应用。

New advances in scanning microscopy and its application to study parasitic protozoa.

作者信息

de Souza Wanderley, Attias Marcia

机构信息

Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Instituto Nacional de Ciência e Tecnologia em Biologia Estrutural e Bioimagens, Centro Nacional de Biologia Estrutural e Bioimagens-CENABIO, Universidade Federal do Rio de Janeiro, CCS-Bloco G, 21941-900 Rio de Janeiro, Brazil.

Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Instituto Nacional de Ciência e Tecnologia em Biologia Estrutural e Bioimagens, Centro Nacional de Biologia Estrutural e Bioimagens-CENABIO, Universidade Federal do Rio de Janeiro, CCS-Bloco G, 21941-900 Rio de Janeiro, Brazil.

出版信息

Exp Parasitol. 2018 Jul;190:10-33. doi: 10.1016/j.exppara.2018.04.018. Epub 2018 Apr 25.

DOI:10.1016/j.exppara.2018.04.018
PMID:29702111
Abstract

Scanning electron microscopy has been used to observe and study parasitic protozoa for at least 40 years. However, field emission electron sources, as well as improvements in lenses and detectors, brought the resolution power of scanning electron microscopes (SEM) to a new level. Parallel to the refinement of instruments, protocols for preservation of the ultrastructure, immunolabeling, exposure of cytoskeleton and inner structures of parasites and host cells were developed. This review is focused on protozoan parasites of medical and veterinary relevance, e.g., Toxoplasma gondii, Tritrichomonas foetus, Giardia intestinalis, and Trypanosoma cruzi, compilating the main achievements in describing the fine ultrastructure of their surface, cytoskeleton and interaction with host cells. Two new resources, namely, Helium Ion Microscopy (HIM) and Slice and View, using either Focused Ion Beam (FIB) abrasion or Microtome Serial Sectioning (MSS) within the microscope chamber, combined to backscattered electron imaging of fixed (chemically or by quick freezing followed by freeze substitution and resin embedded samples is bringing an exponential amount of valuable information. In HIM there is no need of conductive coating and the depth of field is much higher than in any field emission SEM. As for FIB- and MSS-SEM, high resolution 3-D models of areas and volumes larger than any other technique allows can be obtained. The main results achieved with all these technological tools and some protocols for sample preparation are included in this review. In addition, we included some results obtained with environmental/low vacuum scanning microscopy and cryo-scanning electron microscopy, both promising, but not yet largely employed SEM modalities.

摘要

扫描电子显微镜用于观察和研究寄生原生动物至少已有40年历史。然而,场发射电子源以及透镜和探测器的改进,将扫描电子显微镜(SEM)的分辨率提升到了一个新水平。在仪器不断完善的同时,还开发了用于保存超微结构、免疫标记、暴露寄生虫和宿主细胞的细胞骨架及内部结构的方案。本综述聚焦于具有医学和兽医学意义的原生动物寄生虫,如刚地弓形虫、胎儿三毛滴虫、肠贾第虫和克氏锥虫,汇总了在描述其表面、细胞骨架的精细超微结构以及与宿主细胞相互作用方面的主要成果。两种新资源,即氦离子显微镜(HIM)和切片观察技术,通过在显微镜腔内使用聚焦离子束(FIB)研磨或切片机连续切片(MSS),并结合固定样本(化学固定或快速冷冻后进行冷冻置换和树脂包埋)的背散射电子成像,带来了大量有价值的信息。在HIM中无需进行导电涂层处理,且景深比任何场发射SEM都要高得多。至于FIB-SEM和MSS-SEM,可以获得比其他任何技术所能实现的更大区域和体积的高分辨率三维模型。本综述涵盖了所有这些技术工具所取得的主要成果以及一些样本制备方案。此外,我们还纳入了通过环境/低真空扫描显微镜和低温扫描电子显微镜获得的一些结果,这两种技术都很有前景,但尚未得到广泛应用。

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