Sawaguchi A, Aoyama F, Ide S, Suganuma T
Department of Anatomy, Ultrastructural Cell Biology, Faculty of Medicine, University of Miyazaki, Kiyotake, Miyazaki, Japan.
J Microsc. 2009 May;234(2):113-7. doi: 10.1111/j.1365-2818.2009.03161.x.
The goal of specimen preparation for transmission electron microscopy is to obtain high-quality ultra-thin sections with which we can correlate cellular structure to physiological function. In this study, we newly developed a capsule-supporting ring that can be useful for resin embedding of glass-mounted specimens. The present device allowed us to re-embed a semi-thin section on a microscope slide into a resin block not only for efficient ultra-thin sectioning but also for a correlative light and electron microscopy. Similar to epoxy resins for morphological observations, semi-thin sections of low-viscosity hydrophilic resins, such as Lowicryl series, can be re-embedded into the resin, which can be useful for cytochemical gold labelling. A further application of the present device improved flat embedding of cultured cells on glass cover slips for electron microscopy, preserving in situ sub-cellular structures close to their native state. We practically describe the use of capsule-supporting ring and demonstrate representative micrographs as results.
透射电子显微镜标本制备的目标是获得高质量的超薄切片,通过这些切片我们可以将细胞结构与生理功能联系起来。在本研究中,我们新开发了一种胶囊支撑环,可用于玻璃载玻片标本的树脂包埋。该装置使我们能够将显微镜载玻片上的半薄切片重新包埋到树脂块中,不仅有利于高效制备超薄切片,还可用于相关的光镜和电镜观察。与用于形态学观察的环氧树脂类似,低粘度亲水性树脂(如Lowicryl系列)的半薄切片可以重新包埋到树脂中,这对于细胞化学金标记很有用。本装置的进一步应用改进了玻璃盖玻片上培养细胞的平整包埋,用于电子显微镜观察,保留了接近其天然状态的原位亚细胞结构。我们实际描述了胶囊支撑环的使用,并展示了代表性的显微照片作为结果。