首页> 美国卫生研究院文献>Journal of Anatomy and Physiology >Three-dimensional reconstruction of the Meissner corpuscle of man after silver impregnation and immunofluorescence with PGP 9.5 antibodies using confocal scanning laser microscopy.
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Three-dimensional reconstruction of the Meissner corpuscle of man after silver impregnation and immunofluorescence with PGP 9.5 antibodies using confocal scanning laser microscopy.

机译:在银浸渍和PGP 9.5抗体免疫荧光后使用共聚焦扫描激光显微镜对人的迈斯纳小球进行三维重建。

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摘要

The 3-dimensional organisation of the neural component of the human Meissner corpuscle was studied after silver impregnation and following immunofluorescence for protein gene product 9.5 (PGP 9.5) by confocal scanning laser microscopy. The morphology of the Meissner corpuscle was found to show consistent differences depending on the labelling method used. After silver impregnation by the Winkelmann technique the branches of the afferent nerve fibres of the corpuscle showed both thin regions and varicose elements, the latter probably corresponding to the portions rich in mitochondria observed by transmission electron microscopy. The bulkier elements were never more than 5-6 microns in diameter. After immunolabelling for PGP 9.5 the nerve fibre branches in the corpuscle always presented flattened and discoidal expansions with a diameter of up to 30 microns. On the basis of what is known as to the mechanism of action of silver impregnations it is considered that the black precipitate preferentially labels the parts of neurons that are rich in neurofilaments. In any case the precipitate is deposited throughout the neuronal cytoplasm except in the mitochondria and the nucleus. Accordingly, in the varicosities of the Meissner corpuscles that are rich in mitochondria, there is little space for the formation of the precipitate. The use of antiserum against PGP 9.5, which labels the larger proteinaceous component of the axoplasm, demonstrates the complete architecture of the neural component of the Meissner corpuscle, and visualises the discoidal and flattened expansions which are absent in the impregnated corpuscles. It is concluded that immunostaining provides images of the corpuscles, and of peripheral neural structures that are in general closer to reality.
机译:通过共聚焦扫描激光显微镜研究了银浸渍后和蛋白质基因产物9.5(PGP 9.5)的免疫荧光后,研究了人类Meissner小球神经元的3维组织。根据所使用的标记方法,发现迈斯纳小球的形态显示出一致的差异。用Winkelmann技术浸渍银后,小球的传入神经纤维分支均显示出较薄的区域和静脉曲张元素,后者可能对应于通过透射电子显微镜观察到的线粒体丰富的部分。体积较大的元件的直径从未超过5-6微米。在对PGP 9.5进行免疫标记后,小球中的神经纤维分支始终呈扁平状和盘状扩张,直径最大为30微米。基于已知的银浸渍作用机理,认为黑色沉淀物优先标记富含神经丝的神经元部分。在任何情况下,沉淀物都沉积在整个神经元细胞质中,除了线粒体和细胞核。因此,在富含线粒体的迈斯纳小球的静脉曲张中,几乎没有形成沉淀的空间。抗PGP 9.5的抗血清的使用,它标记了轴突的较大蛋白质成分,证明了迈斯纳小体神经成分的完整结构,并可视化了浸渍小体中不存在的盘状和扁平状扩展。结论是,免疫染色提供了小体以及通常更接近于现实的周围神经结构的图像。

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