Jhaveri S, Morest D K
Neuroscience. 1982 Apr;7(4):855-70. doi: 10.1016/0306-4522(82)90047-1.
The development of the auditory nerve endings and their target cells in nucleus magnocellularis was studied by electron microscopy of perfusion-fixed brains from embryonic day 12 to hatching. Embryonic days 12-13: somatic processes extend from the perikaryon. The cytoplasm of the soma and processes contains free ribosomes, mitochondria, lysosomes, rough endoplasmic reticulum, Golgi apparatus and an eccentric, heterochromatic nucleus. Small profiles of auditory nerve fibers containing round, clear vesicles make specialized contacts, including some synapses, on distal somatic processes but rarely on proximal somatic processes or on the soma. The postsynaptic zones contain a flocculent matrix. Days 15-17: somatic processes disappear and occasional attachment plaques are seen between cell bodies. The nucleus appears euchromatic. Cytoplasmic organelles form a dense matrix indicative of intense metabolic activity. Somatic spines are evident. The afferent axons form large, vesiculated profiles located, increasingly, on the cell body and somatic spines, with many points of synaptic contact. Opposite each ending a band of amorphous, flocculent material fills the postsynaptic cytoplasm. Embryonic day 18-hatching: the somatic cytoplasm becomes less dense; stacks of rough endoplasmic reticulum start to condense. Afferent axon terminals mature, especially the synaptic membrane complex and associated densities. The postsynaptic flocculent material diminishes in extent until it is found associated only with somatic spines. The ultrastructural observations on the maturation of nucleus magnocellularis closely corroborate and extend previous results with the Golgi methods. Developing auditory nerve fibers initially synapse on the distal parts of the somatic processes of the immature cells. As the somatic processes disappear or retract, axonal endings move to the soma and develop into large axosomatic end-bulbs. Possibly, the somatic processes as they retract drag the auditory nerve endings to the cell body. The findings also suggest a role of the transiently appearing, flocculent material of the postsynaptic regions in the formation of synapses.
通过对胚胎第12天至孵化期灌注固定脑的电子显微镜观察,研究了大细胞神经核中听神经末梢及其靶细胞的发育情况。胚胎第12 - 13天:体细胞突起从胞体伸出。胞体和突起的细胞质含有游离核糖体、线粒体、溶酶体、粗面内质网、高尔基体和一个偏心的、异染色质的细胞核。含有圆形清亮小泡的听神经纤维小轮廓在体细胞突起远端形成特殊接触,包括一些突触,但很少在近端体细胞突起或胞体上形成接触。突触后区含有絮状基质。第15 - 17天:体细胞突起消失,细胞体之间可见偶尔的附着斑。细胞核呈常染色质。细胞质细胞器形成致密基质,表明代谢活动旺盛。体细胞棘明显。传入轴突形成大的、有小泡的轮廓,越来越多地位于细胞体和体细胞棘上,有许多突触接触点。在每个末梢相对处,一条无定形、絮状物质带充满突触后细胞质。胚胎第18天至孵化期:体细胞细胞质密度降低;粗面内质网堆叠开始浓缩。传入轴突终末成熟,尤其是突触膜复合体和相关的致密物。突触后絮状物质范围缩小,直至仅在体细胞棘处发现。对大细胞神经核成熟的超微结构观察密切证实并扩展了先前用高尔基方法得到的结果。发育中的听神经纤维最初在未成熟细胞体细胞突起的远端形成突触。随着体细胞突起消失或缩回,轴突末梢移向胞体并发育成大的轴体终球。可能是体细胞突起缩回时将听神经末梢拖向细胞体。这些发现还表明突触后区域短暂出现的絮状物质在突触形成中起作用。