Peters A, Sethares C
Department of Anatomy and Neurobiology, Boston University School of Medicine, Massachusetts 02118.
J Comp Neurol. 1991 Apr 1;306(1):1-23. doi: 10.1002/cne.903060102.
In sections of area 17 of monkey visual cortex treated with an antibody to MAP2 the disposition of the cell bodies and dendrites of the neurons is readily visible. In such preparations it is evident that the apical dendrites of the pyramidal cells of layer VI form fascicles that pass into layer IV, where most of them gradually taper and form their terminal tufts. In contrast, the apical dendrites of the smaller layer V pyramidal cells come together in a more regular fashion. They form clusters that pass through layer IV and into layer II/III where the apical dendrites of many of the pyramidal cells in that layer add to the clusters. In horizontal sections taken through the middle of layer IV, these clusters of apical dendrites are found to have an average center-to-center spacing of about 30 microns, and it is proposed that each cluster of apical dendrites represents the axis of a module of pyramidal cells that has a diameter of about 30 microns and contains about 142 neurons. The MAP2 antibody reaction also reveals that some pyramidal cells in layers IVA and IVB have their cell bodies arranged into cones. There are about 118 such cones beneath 1 mm2 of cortical surface and the apical dendrites of the pyramidal cells within them bundle together at the apex of each cone to pass into layer III. Surrounding the cones of neurons there are horizontally aligned, thin dendrites. The location of these dendrites coincides with the dark walls of the honeycomb pattern seen in layer IVA after cytochrome oxidase reactions, or after the parvocellular input from the lateral geniculate nucleus has been labeled. Thus the cones of pyramidal cells within upper layer IV fit into the pockets of the honeycomb pattern. Below the cones of pyramidal cells are the outer Meynert cells within layer IVB, and the cell bodies of these large neurons are disposed so that they preferentially lie beneath the neuropil between the cones of pyramids. It is suggested that pyramidal cell modules are a basic feature of the cerebral cortex, and that these are combined together by afferent inputs to the cortex to generate the systems of functional columns.
在用针对微管相关蛋白2(MAP2)的抗体处理的猴视觉皮层17区切片中,神经元的细胞体和树突的分布清晰可见。在这样的标本中,很明显,VI层锥体细胞的顶端树突形成束状,进入IV层,其中大多数逐渐变细并形成终末簇。相比之下,较小的V层锥体细胞的顶端树突以更规则的方式聚集在一起。它们形成簇,穿过IV层进入II/III层,该层中许多锥体细胞的顶端树突加入这些簇中。在通过IV层中部的水平切片中,发现这些顶端树突簇的中心到中心的平均间距约为30微米,并且有人提出,每个顶端树突簇代表一个直径约为30微米、包含约142个神经元的锥体细胞模块的轴。MAP2抗体反应还显示,IVA层和IVB层中的一些锥体细胞的细胞体排列成锥体。在1平方毫米的皮质表面下方约有118个这样的锥体,其中锥体细胞的顶端树突在每个锥体的顶端聚集在一起,进入III层。在神经元锥体周围有水平排列的细树突。这些树突的位置与细胞色素氧化酶反应后或外侧膝状体核的小细胞输入被标记后在IVA层中看到的蜂窝状图案的暗壁重合。因此,上层IV内的锥体细胞锥体与蜂窝状图案的凹陷相契合。在锥体细胞锥体下方是IVB层内的外迈内特细胞,这些大神经元的细胞体排列方式使得它们优先位于锥体之间的神经毡下方。有人提出,锥体细胞模块是大脑皮层的一个基本特征,并且这些模块通过传入到皮层的输入组合在一起,以产生功能柱系统。