Kimmel C B, Sessions S K, Kimmel R J
J Comp Neurol. 1981 May 1;198(1):101-20. doi: 10.1002/cne.901980110.
The shape of the Mauthner neuron (M-neuron) and the distribution of its afferent synapses were studied between days 2 and 6 after fertilization in the zebrafish Brachydanio rerio. This interval is just after the outgrowth of M-dendrites begins, and during this time the M-cell acquires its definitive shape. The M-cell has two large invariant dendrites: The lateral dendrite terminates in the sensory neuropil of the acoustico-lateral area, and th ventral dendrite terminates in the neuropil of the motor tegmentum. Fine dendrites are present, and mostly arise from three regions; from the terminus of each major dendrite and from the ventral surface of the perikaryon. The number and position of fine dendrites within each of these sets is variable, even among animals from a single isogenic clone. M-cells with improper numbers or positions of large dendrites were never encountered, even early in development. This suggests that their outgrowth is a highly directed process. Large numbers of afferent synapses are formed on the M-cell during the time of dendrite outgrowth. By day 6 there is a mosaic pattern of morphologically distinctive terminals that is similar to the pattern of the adult goldfish M-cell. Identified categories of terminals include (1) myelinated club endings, on the distal part of the lateral dendrite, (2) boutons, on the dendrites and perikaryon, (3) unmyelinated club endings, on the dorsomedial portion of the perikaryon adjacent to the axon cap, and (4) spiral fiber terminals within the axon cap. The nonrandom nature of the input may be ascertained by observing the distribution of electrotonic or gap junctions on the cell surface. These are frequently encountered on the initial segment of the axon (spiral fiber terminals), ventral dendrite and ventral perikaryon (boutons), and distal lateral dendrite (myelinated club endings). Gap junctions are only rarely observed on the dorsal surface of the cell, although this region, like others of the cell, receives large numbers of chemical synaptic contacts. This pattern is similar at all stages studied, which suggests that no large rearrangements in synaptic contacts occur during this developmental period. We discuss these observations in relation to the hypothesis that patterned dendritic growth of the M-cell is directed by synaptic interactions with the afferents.
在斑马鱼短盖巨脂鲤受精后的第2天至第6天,研究了莫特纳尔神经元(M神经元)的形态及其传入突触的分布。这个时间段刚好是M树突开始生长之后,在此期间M细胞获得其最终形态。M细胞有两个大的不变树突:外侧树突终止于听侧区的感觉神经毡,腹侧树突终止于运动被盖的神经毡。存在细树突,且大多起源于三个区域:每个主要树突的末端以及胞体的腹面。即使在来自单个同基因克隆的动物中,这些组中每组细树突的数量和位置也是可变的。从未遇到过大树突数量或位置不当的M细胞,即使在发育早期也是如此。这表明它们的生长是一个高度定向的过程。在树突生长期间,M细胞上形成了大量传入突触。到第6天,出现了形态上独特的终末的镶嵌模式,这与成年金鱼M细胞的模式相似。已确定的终末类别包括:(1)有髓棒状终末,位于外侧树突的远端部分;(2)钮扣状小体,位于树突和胞体上;(3)无髓棒状终末,位于靠近轴突帽的胞体背内侧部分;(4)轴突帽内的螺旋纤维终末。输入的非随机性质可以通过观察细胞表面电紧张连接或缝隙连接的分布来确定。这些连接在轴突的起始段(螺旋纤维终末)、腹侧树突和腹侧胞体(钮扣状小体)以及外侧树突远端(有髓棒状终末)经常遇到。在细胞的背表面很少观察到缝隙连接,尽管该区域与细胞的其他区域一样接受大量化学突触接触。在所有研究阶段这种模式都是相似的,这表明在这个发育时期突触接触没有发生大的重新排列。我们结合M细胞的模式化树突生长由与传入神经元的突触相互作用所指导这一假设来讨论这些观察结果。