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在经冷冻置换、用Lowicryl K11M包埋的大鼠嗅觉受体细胞中,用蛋白G-金对嗅觉标记蛋白进行电子显微镜显示。

Electron-microscopic demonstration of olfactory-marker protein with protein G-gold in freeze-substituted, Lowicryl K11M-embedded rat olfactory-receptor cells.

作者信息

Menco B P

机构信息

Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois.

出版信息

Cell Tissue Res. 1989;256(2):275-81. doi: 10.1007/BF00218884.

Abstract

In this study electron-microscopic immunocytochemistry was used to localize olfactory marker protein in olfactory epithelia. Rat olfactory-epithelial samples were rapidly frozen, freeze-substituted with acetone, embedded at low temperatures with Lowicryl K11M and labelled on the sections with polyclonal antibodies raised against olfactory marker protein and with protein G conjugated to colloidal gold. Apart from the aforementioned use of acetone, substitution was carried out in the complete absence of chemical fixation, i.e., neither aldehydes nor OsO4 were used. This procedure resulted in localization concurrent with a good ultrastructural preservation. Olfactory-marker protein was present throughout the cytoplasmic compartments of dendrites and dendritic endings of olfactory-receptor cells, but it was not found in organelles such as mitochondria. Olfactory-marker protein was found only in dendritic endings of olfactory-receptor cells mature enough to have given rise to cilia, but these cilia displayed less labelling than dendrites and dendritic endings. Olfactory-marker protein was not found in apices and microvilli of neighboring olfactory-supporting cells.

摘要

在本研究中,采用电子显微镜免疫细胞化学方法对嗅觉上皮中的嗅觉标记蛋白进行定位。将大鼠嗅觉上皮样本快速冷冻,用丙酮进行冷冻置换,在低温下用Lowicryl K11M包埋,并在切片上用针对嗅觉标记蛋白的多克隆抗体以及与胶体金偶联的蛋白G进行标记。除上述丙酮的使用外,置换过程完全没有进行化学固定,即既未使用醛类也未使用四氧化锇。该方法在良好的超微结构保存的同时实现了定位。嗅觉标记蛋白存在于嗅觉受体细胞树突和树突末梢的整个细胞质区域,但在诸如线粒体等细胞器中未发现。仅在成熟到足以产生纤毛的嗅觉受体细胞的树突末梢中发现了嗅觉标记蛋白,但这些纤毛的标记比树突和树突末梢少。在相邻嗅觉支持细胞的顶端和微绒毛中未发现嗅觉标记蛋白。

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