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负鼠的面神经运动核:细胞学与轴体突触

The facial motor nucleus of the opossum: cytology and axosomatic synapses.

作者信息

Falls W M, King J S

出版信息

J Comp Neurol. 1976 May 15;167(2):177-204. doi: 10.1002/cne.901670205.

DOI:10.1002/cne.901670205
PMID:932239
Abstract

The normal cytology and synaptic organization of the opossum facial motor nucleus was determined by use of Nissl preparations, Golgi impregnations, one-micron plastic sections and electron microscopy. Neurons from all regions of the nucleus can be classified into three categories based on the size and shape of their perikarya, the distribution of Nissl substance and extent of their dendritic arbors. Large neurons (30--50 mu) exhibit numerous Nissl granules and their dendrites often span more than one-half the width of the nucleus in the transverse plane. Their proximal dendrites measure 4--7 mu in diameter, taper to 0.5--2 mu and display few spines. Medium neurons (20--30 mu) can be distinguished from the large nerve cells by their size and their less extensive dendritic arbor. Proximal dendrites measure 4--7 mu in diameter, tapes to 0.5--2 mu and are relativel aspinous. Small neurons (10--20 mu) display a thin rim of cytoplasm which is either uniformly basophilic or achromatic. The dendrites of these neurons are relatively unbranched and taper from 4--5 mu proximally to 0.5--2 mu distally. Their axons give off one or two collaterals within the nuclear borders. More than one-half the perikaryal membrane of large and medium neurons is covered by presynaptic profiles which were grouped into three primary categories based upon differences in their vesicle shape (spherical, pleomorphic, or ellipsoidal). Only a few axosomatic contacts are present on small neurons. Further differentiation of axosomatic synaptic endings is suggested by differences in vesicle size, in pre- and postsynaptic membrane densities and in the size of the synaptic terminals. Vesicle size was determined by a cybergraphic tablet and a PDP-12 computer system and is expressed as a mean area in nm2.

摘要

通过使用尼氏染色制剂、高尔基浸染法、1微米塑料切片和电子显微镜,确定了负鼠面神经运动核的正常细胞学和突触组织。根据核周体的大小和形状、尼氏体物质的分布以及树突分支的范围,可将来自该核所有区域的神经元分为三类。大型神经元(30 - 50微米)有大量尼氏颗粒,其树突在横切面上通常跨越核宽度的一半以上。它们的近端树突直径为4 - 7微米,逐渐变细至0.5 - 2微米,且很少有棘。中型神经元(20 - 30微米)可通过其大小和较不广泛的树突分支与大型神经细胞区分开来。近端树突直径为4 - 7微米,逐渐变细至0.5 - 2微米,相对无棘。小型神经元(10 - 20微米)有一层薄的细胞质边缘,要么均匀嗜碱性,要么无色。这些神经元的树突分支相对较少,从近端的4 - 5微米逐渐变细至远端的0.5 - 2微米。它们的轴突在核边界内发出一两个侧支。大型和中型神经元的核周体膜有一半以上被突触前成分覆盖,根据其囊泡形状(球形、多形性或椭圆形)的差异,这些突触前成分可分为三大类。小型神经元上只有少数轴体接触。囊泡大小、突触前和突触后膜密度以及突触终末大小的差异表明轴体突触末梢存在进一步分化。囊泡大小通过数字绘图板和PDP - 12计算机系统测定,并以平方纳米的平均面积表示。

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