Fujiwara T, Shimizu D, Kon K, Isshiki N, Tsunokuni H, Aoyagi S
Laboratory Animal Center, Ehime University School of Medicine, Shigenobu, Japan.
J Electron Microsc (Tokyo). 2000;49(4):551-8. doi: 10.1093/oxfordjournals.jmicro.a023843.
Cell marking is widely used to examine cell development and differentiation in developmental biology. We developed a new method for localizing cell markers in a semi-thin epoxy section with scanning electron microscopy. Cultured fibroblasts ingesting carbon particles were autologously transplanted into a rabbit transparent ear chamber, 6 mm in diameter and 100 microm in depth. Eight days after the transplantation, tissues in the chamber were fixed and embedded in epoxy resin. Semi-thin sections were cut and stained with toluidine blue. Fibroblasts in connective tissues which contained black spots were observed with a light microscope. These sections were subsequently ion-etched with an ion-coater and coated with platinum. The same fibroblasts were then visualized by secondary electron imaging using a scanning electron microscope. A nucleus with nuclear envelope, nuclear pores, a nucleolus and heterochromatin, mitochondria with cristae and rough endoplasmic reticulum were observed in the fibroblasts. The black spots in the fibroblasts were identified as bright bodies with the scanning electron microscope. The bright bodies were found to be a lump of tiny particles less than 100 nm in diameter. In order to analyse such particles with energy dispersive X-ray microanalysis, ion-etched sections were coated with carbon. X-ray energy spectrometry clearly demonstrated that these were carbon particles, which had been endocytosed by the fibroblast. This suggests that scanning electron microscopy combined with energy dispersive X-ray microanalysis is useful for detecting carbon particles in the cytoplasm at an ultrastructural level in semi-thin epoxy sections subsequent to ion etching and that this method may be applicable to other cell markers, such as gold particles to track cells in the field of cell development and cell differentiation.
细胞标记在发育生物学中被广泛用于研究细胞的发育和分化。我们开发了一种利用扫描电子显微镜在半薄环氧树脂切片中定位细胞标记物的新方法。将摄取碳颗粒的培养成纤维细胞自体移植到直径6毫米、深度100微米的兔透明耳室中。移植8天后,将耳室内的组织固定并包埋在环氧树脂中。切取半薄切片并用甲苯胺蓝染色。用光学显微镜观察结缔组织中含有黑点的成纤维细胞。随后,这些切片用离子镀膜机进行离子蚀刻并镀上铂。然后使用扫描电子显微镜通过二次电子成像观察相同的成纤维细胞。在成纤维细胞中观察到了带有核膜、核孔、核仁以及异染色质的细胞核,带有嵴的线粒体和粗面内质网。用扫描电子显微镜观察发现,成纤维细胞中的黑点为明亮体。这些明亮体被发现是直径小于100纳米的微小颗粒团块。为了用能量色散X射线微分析来分析这些颗粒,离子蚀刻后的切片镀上了碳。X射线能谱分析清楚地表明这些是被成纤维细胞内吞的碳颗粒。这表明,扫描电子显微镜结合能量色散X射线微分析可用于在离子蚀刻后的半薄环氧树脂切片的超微结构水平上检测细胞质中的碳颗粒,并且这种方法可能适用于其他细胞标记物,如用于细胞发育和细胞分化领域追踪细胞的金颗粒。