Coulter H D
Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis 55455.
Proc Natl Acad Sci U S A. 1988 Sep;85(18):7028-32. doi: 10.1073/pnas.85.18.7028.
The distribution of enkephalin immunoreactivity in the neuropil of globus pallidus was analyzed with a quick-freezing, postembedment-staining technique for light and electron microscopic immunocytochemistry. Fluorescence images of ultrathin sections on glass slides, obtained with a silicon-intensified-tube (type) video camera, revealed staining in the form of scattered fluorescent dots, each 200-400 nm in diameter. Colloidal gold staining under the electron microscope was associated with 80- to 100-nm vesicles of average electron density, widely dispersed in the neuropil, with usually one and no more than four vesicles in individual sectioned neuronal processes. Analysis of fluorescence images in paired serial sections of thicknesses varying from 25 to 150 nm proved that the 200- to 400-nm dots of fluorescence came from smaller structures, presumably the 80- to 100-nm vesicles. Enkephalinergic vesicles in the globus pallidus were nearly always found in what appeared to be axons of passage and were only infrequently associated with synaptic profiles.
采用快速冷冻、包埋后染色技术进行光镜和电镜免疫细胞化学分析,研究脑啡肽免疫反应性在苍白球神经毡中的分布。用硅增强型管(型)摄像机获取载玻片上超薄切片的荧光图像,显示为散在的荧光点,每个直径为200 - 400nm。电镜下胶体金染色与平均电子密度的80 - 100nm囊泡相关,这些囊泡广泛分布于神经毡中,在单个切片的神经元突起中通常有一个且不超过四个囊泡。对厚度从25到150nm的配对连续切片的荧光图像分析表明,200 - 400nm的荧光点来自较小的结构,推测为80 - 100nm的囊泡。苍白球中的脑啡肽能囊泡几乎总是出现在看似过路轴突中,很少与突触结构相关。