Gibbins I L, Rodgers H F, Matthew S E, Murphy S M
Department of Anatomy and Histology and Centre for Neuroscience, Flinders University of South Australia, Adelaide, Australia.
J Comp Neurol. 1998 Dec 21;402(3):285-302.
The authors serially sectioned seven dye-filled neuronal somata and more than 1.6 mm of their dendrites from the lumbar sympathetic ganglia of guinea pigs and examined them ultrastructurally to determine the distribution of preganglionic synaptic inputs to their dendrites and cell bodies. Most of the surface of the neurons was covered with Schwann cells. Apposing boutons were rare, with an average density of one axosomatic bouton per 125 microm2 of somatic membrane and one axodendritic bouton per 25 microm of dendrite. Many dendritic segments that were more than 50 microm long completely lacked any apposing boutons. Although the average density of apposing boutons was low, local densities could be high, so that clusters of up to four adjacent boutons occurred on cell bodies and dendrites alike. The spatial arrangement of the apposing boutons for each of the cells examined here was not significantly different from a random distribution. Consequently, the number of apposing boutons observed for any neuron was simply proportional to the amount of neuronal surface sampled in the serial section run. About 50% of boutons directly apposing the neurons lacked any detectable presynaptic specialisations. When they were present, the presynaptic densities had a mean length of about 220 nm, with no difference between boutons that made axosomatic or axodendritic appositions. By applying these data to complete reconstructions of the dendritic trees of dye-filled sympathetic neurons at the light microscopic level, the authors estimated that few neurons in the lumbar sympathetic chain of guinea pigs would receive more than 200 synapses or apposing boutons and that many of them would receive less than 100 synapses. Up to 50% of these boutons would be predicted to make axosomatic contacts. These new observations provide a strong morphological framework for a better understanding of how sympathetic final motor neurons process their preganglionic synaptic inputs.
作者对豚鼠腰交感神经节中7个充满染料的神经元胞体及其超过1.6毫米的树突进行了连续切片,并对其进行超微结构检查,以确定节前突触输入在其树突和胞体上的分布。神经元的大部分表面都被施万细胞覆盖。相邻的终扣很少见,平均密度为每125平方微米的胞体膜有一个轴体终扣,每25微米的树突有一个轴树终扣。许多长度超过50微米的树突节段完全没有相邻的终扣。虽然相邻终扣的平均密度较低,但局部密度可能较高,以至于在胞体和树突上都出现了多达四个相邻终扣的簇。此处检查的每个细胞的相邻终扣的空间排列与随机分布没有显著差异。因此,在连续切片中观察到的任何神经元的相邻终扣数量仅与采样的神经元表面面积成正比。直接与神经元相邻的终扣中约50%没有任何可检测到的突触前特化结构。当存在突触前特化结构时,突触前致密区的平均长度约为220纳米,轴体或轴树突触的终扣之间没有差异。通过将这些数据应用于在光学显微镜水平上对充满染料的交感神经元树突树的完整重建,作者估计豚鼠腰交感神经链中很少有神经元会接受超过200个突触或相邻终扣,而且其中许多神经元接受的突触少于100个。预计这些终扣中多达50%会形成轴体接触。这些新观察结果为更好地理解交感运动终末神经元如何处理节前突触输入提供了一个强大的形态学框架。