Meskenaite V
Institut für Neuroinformatik University of Zürich/ETH, Switzerland.
J Comp Neurol. 1997 Mar 3;379(1):113-32.
The connections of local circuit neurons immunoreactive for calcium-binding protein calretinin (CR-ir) were studied in area 17 of the macaque monkey visual cortex. Most CR-ir neurons were located in layers 2 and 3A. They were polymorphic and included bitufted, multipolar, pyramid-shaped neurons with smooth dendrites and Cajal-Retzius cells. The majority of CR-ir neurons were gamma-aminobutyric acid (GABA)-immunopositive (approximately 90%), and compromised about 14% of the total GABAergic neuron population. The axons of CR-ir cells had local arbors within layers 1-3, but the major trunks descended to deep layers 5 and 6 where they formed dense terminal fields within narrow columns (100-150 microns). This specific innervation of layers 5 and 6 appeared as a distinct feature of area 17 as it was not seen in the adjacent area 18. CR-ir boutons (n = 168) were GABA-ir (95%) and formed symmetric synapses. In layers 1-3, the majority of postsynaptic targets (n = 64) were GABAergic local circuit neurons [postsynaptic target distribution: GABA-positive dendrites (67%) and somata (14%), and GABA-negative dendrites (13%) and spines (6%)]. In deep layers, the most synapses (80%; n = 187) were formed with pyramidal cells where they provided a basket-type innervation [postsynaptic target distribution: GABA-positive dendrites (19%) and somata (1%), and GABA-negative dendrites (50%), spines (20%) and somata (10%)]. Unlike other GABAergic neurons, which innervate mainly pyramidal neurons, the CR-ir subpopulation only has pyramids as a preferred target in the deep layers (layers 5 and 6); however, in the superficial layers of the area 17, selectively form synapses mainly with other GABAergic cells. Thus, the CR-ir neurons appear to have a dual function of disinhibiting superficial layer neurons and inhibiting pyramidal output neurons in the deep layers.
在猕猴视觉皮层17区研究了对钙结合蛋白钙视网膜蛋白(CR免疫反应阳性)的局部回路神经元的连接情况。大多数CR免疫反应阳性神经元位于第2层和第3A层。它们形态多样,包括双簇状、多极、具有光滑树突的金字塔形神经元以及Cajal-Retzius细胞。大多数CR免疫反应阳性神经元γ-氨基丁酸(GABA)免疫阳性(约90%),约占GABA能神经元总数的14%。CR免疫反应阳性细胞的轴突在第1 - 3层内有局部分支,但主要主干向下延伸至深层的第5层和第6层,在那里它们在狭窄柱体(100 - 150微米)内形成密集的终末场。第5层和第6层的这种特定神经支配是17区的一个明显特征,因为在相邻的18区未观察到。CR免疫反应阳性终扣(n = 168)为GABA免疫反应阳性(95%),并形成对称突触。在第1 - 3层,大多数突触后靶点(n = 64)是GABA能局部回路神经元[突触后靶点分布:GABA阳性树突(67%)和胞体(14%),以及GABA阴性树突(13%)和棘(6%)]。在深层,大多数突触(80%;n = 187)与锥体细胞形成,提供篮状神经支配[突触后靶点分布:GABA阳性树突(19%)和胞体(1%),以及GABA阴性树突(50%)、棘(20%)和胞体(10%)]。与主要支配锥体细胞的其他GABA能神经元不同,CR免疫反应阳性亚群在深层(第5层和第6层)仅将锥体神经元作为首选靶点;然而,在17区的浅层,主要选择性地与其他GABA能细胞形成突触。因此,CR免疫反应阳性神经元似乎具有双重功能,即解除浅层神经元的抑制并抑制深层的锥体输出神经元。