Kincaid A E, Zheng T, Wilson C J
Department of Anatomy and Neurobiology, University of Tennessee College of Medicine, Memphis, Tennessee 38163, USA.
J Neurosci. 1998 Jun 15;18(12):4722-31. doi: 10.1523/JNEUROSCI.18-12-04722.1998.
The distribution of synapses formed by corticostriatal neurons was measured to determine the average connectivity and degree of convergence of these neurons and to search for spatial inhomogeneities. Two kinds of axonal fields, focal and extended, and two striatal tissue compartments, the patch (striosome) and matrix, were analyzed separately. Electron microscopic examination revealed that both kinds of corticostriatal axons made synapses at varicosities that could be identified in the light microscope, and each varicosity made a single synapse. Thus, the distribution of varicosities was a good estimate of the spatial distribution of synapses. The distance between axonal varicosities was measured to determine the density of synaptic connections formed by one axon within the volume occupied by a striatal neuron. Intersynaptic distances were distributed exponentially, except that synapses were rarely located <4 microm apart. The mean distance between synapses was approximately 10 microm, so axons made a maximum of 40 synapses within the dendritic volume of a spiny neuron. There are approximately 2840 spiny neurons located within the volume of the dendrites of one spiny cell (Oorschot, 1996), so each axon must contact </=1.4% of all cells in its axonal arborization. Within the same volume there are approximately 30.5 million asymmetric synapses (Ingham et al., 1996), approximately half of which are cortical in origin. Thus, approximately 380,000 cortical axons innervate the volume of the dendritic tree of one spiny cell. Striatal neurons with totally overlapping dendritic volumes have few presynaptic cortical axons in common, and cortical cells with overlapping axons have few striatal target neurons in common. These results explain the absence of redundancy in the responses of neurons located near each other in the striatum.
测量皮质纹状体神经元形成的突触分布,以确定这些神经元的平均连接性和汇聚程度,并寻找空间不均匀性。分别分析了两种轴突场,即局灶性和扩展性轴突场,以及两个纹状体组织区室,即斑块(纹状体小体)和基质。电子显微镜检查显示,两种皮质纹状体轴突都在光镜下可识别的膨体处形成突触,且每个膨体形成一个单一突触。因此,膨体的分布很好地估计了突触的空间分布。测量轴突膨体之间的距离,以确定一条轴突在纹状体神经元所占体积内形成的突触连接密度。突触间距离呈指数分布,只是突触很少位于相距小于4微米的位置。突触间的平均距离约为10微米,因此轴突在一个棘状神经元的树突体积内最多形成40个突触。在一个棘状细胞的树突体积内大约有2840个棘状神经元(奥肖特,1996年),所以每条轴突在其轴突分支中必须接触到所有细胞的≤1.4%。在相同体积内大约有3050万个不对称突触(英厄姆等人,1996年),其中大约一半起源于皮质。因此,大约380000条皮质轴突支配一个棘状细胞的树突树体积。树突体积完全重叠的纹状体神经元很少有共同的突触前皮质轴突,而轴突重叠的皮质细胞很少有共同的纹状体靶神经元。这些结果解释了纹状体中彼此相邻的神经元反应中不存在冗余的现象。