DeFelipe J, Hendry S H, Hashikawa T, Molinari M, Jones E G
Department of Anatomy and Neurobiology, University of California, Irvine 92717.
Neuroscience. 1990;37(3):655-73. doi: 10.1016/0306-4522(90)90097-n.
Immunocytochemical methods were used to study 28,000 mol. wt calbindin and tachykinin immunoreactivity in the monkey cerebral cortex. Calbindin and tachykinin immunoreactivity give rise to a generally different pattern of staining of cell bodies and terminal-like puncta. However, the staining of long, vertically-oriented bundles of processes--identical to classical double bouquet cell axonal arborizations--is the most prominent feature of the pattern of both calbindin- and tachykinin-immunoreactive staining. These bundles form a widespread and regular columnar system descending from layer II to layers III-V. The bundles are most evident in layer III where, in tangential sections, they have a density of 7-15 bundles/10,000 microns 2 with a center-to-center spacing of 15-30 microns. The distribution of immunoreactive bundles through the cortex is not homogeneous; somatic sensory, auditory, and visual areas display a large number of calbindin-immunoreactive bundles while tachykinin-immunoreactive bundles are only numerous in the auditory areas and in area 18 of the visual cortex. In the motor cortex (area 4) few or no immunoreactive bundles are visualized with either antibody. Correlative light and electron microscope analysis of tachykinin immunoreactive bundles in the primary auditory cortex shows that the tachykinin-positive axons of the bundles form symmetrical synaptic contacts with dendritic shafts (57%) and spines (43%). Frequently, several immunoreactive boutons that arise from the same fiber are seen climbing along the surfaces of vertically-oriented, non-immunoreactive processes which include myelinated and unmyelinated axons and probably glial processes. The same ultrastructural features and a similar synaptic distribution were found in a previous study [DeFelipe et al. (1989) Brain Res. 503, 49-54] of calbindin-positive bundles in the somatic sensory cortex (areas 3a and 1). Despite the virtually identical morphological features of tachykinin- and calbindin-immunoreactive bundles, colocalization studies demonstrate little coexistence of the two antigens in somata and none in the axonal bundles of double bouquet cells. These data suggest that the double bouquet cell is a chemically heterogeneous, but ubiquitous morphological type of cortical interneuron, whose uniquely bundled axonal system, which is probably GABAergic, imposes a fundamental microcolumnar organization upon the cerebral cortex.
采用免疫细胞化学方法研究了猴大脑皮质中分子量为28,000的钙结合蛋白和速激肽免疫反应性。钙结合蛋白和速激肽免疫反应性在细胞体和终末样小点的染色模式上通常有所不同。然而,长的、垂直排列的突起束(与经典的双花束状细胞轴突分支相同)的染色是钙结合蛋白和速激肽免疫反应性染色模式中最突出的特征。这些束形成一个广泛且规则的柱状系统,从II层向下延伸至III - V层。这些束在III层最为明显,在该层的水平切片中,其密度为7 - 15束/10,000平方微米,中心间距为15 - 30微米。免疫反应性束在整个皮质中的分布并不均匀;躯体感觉、听觉和视觉区域显示出大量的钙结合蛋白免疫反应性束,而速激肽免疫反应性束仅在听觉区域和视觉皮质的18区较多。在运动皮质(4区),用任何一种抗体都很少或看不到免疫反应性束。对初级听觉皮质中速激肽免疫反应性束进行的相关光镜和电镜分析表明,束中的速激肽阳性轴突与树突干(57%)和树突棘(43%)形成对称突触联系。经常可以看到,同一纤维发出的几个免疫反应性终扣沿着垂直排列的非免疫反应性突起表面攀爬,这些突起包括有髓和无髓轴突,可能还有神经胶质突起。在先前一项关于躯体感觉皮质(3a区和1区)中钙结合蛋白阳性束的研究[DeFelipe等人(1989年),《脑研究》503,49 - 54]中发现了相同的超微结构特征和类似的突触分布。尽管速激肽和钙结合蛋白免疫反应性束的形态特征几乎相同,但共定位研究表明,这两种抗原在细胞体中很少共存,在双花束状细胞的轴突束中则不存在共存。这些数据表明,双花束状细胞是一种化学性质异质但普遍存在的皮质中间神经元形态类型,其独特的成束轴突系统可能是γ-氨基丁酸能的,在大脑皮质中形成了基本的微柱状组织。