Castano P, Rumio C, Morini M, Miani A, Castano S M
Institute of Human Anatomy, University of Milan, Italy.
J Anat. 1995 Apr;186 ( Pt 2)(Pt 2):261-70.
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.
通过共聚焦扫描激光显微镜,在银浸染及对蛋白质基因产物9.5(PGP 9.5)进行免疫荧光标记后,对人迈斯纳小体神经成分的三维结构进行了研究。发现迈斯纳小体的形态根据所使用的标记方法呈现出一致的差异。采用温克尔曼技术进行银浸染后,小体传入神经纤维的分支显示出细的区域和曲张元件,后者可能对应于透射电子显微镜下观察到的富含线粒体的部分。较粗大的元件直径从不超过5 - 6微米。对PGP 9.5进行免疫标记后,小体内的神经纤维分支总是呈现出扁平的盘状膨大,直径可达30微米。基于已知的银浸染作用机制,认为黑色沉淀物优先标记富含神经丝的神经元部分。无论如何,沉淀物沉积在整个神经元细胞质中,线粒体和细胞核除外。因此,在富含线粒体的迈斯纳小体曲张部分,沉淀物形成的空间很小。使用针对PGP 9.5的抗血清,它标记轴浆中较大的蛋白质成分,展示了迈斯纳小体神经成分的完整结构,并使浸染小体中不存在的盘状和平坦膨大可视化。得出的结论是,免疫染色提供的小体及周围神经结构的图像总体上更接近实际情况。