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通过电子显微镜放射自显影术确定再生神经元轴浆运输过程中亮氨酸-³H的分布。

Distribution of leucine- 3 H during axoplasmic transport within regenerating neurons as determined by electron-microscope radioautography.

作者信息

Lentz T L

出版信息

J Cell Biol. 1972 Mar;52(3):719-32. doi: 10.1083/jcb.52.3.719.

Abstract

The distribution of leucine-(3)H in neurons was determined by electron-microscope radioautography after infusion of label into the spinal cord or sensory ganglia of regenerating newts. In the nerve cell bodies 3 days after infusion, the highest concentration of label per unit area occurred over the rough-surfaced endoplasmic reticulum. In the large brachial nerves, the silver grains were not distributed uniformly in the axoplasm, indicating that the labeled materials are restricted in their movement to certain regions of the axon. Almost all of the radioautographic grains observed in myelinated nerves could be accounted for by the presence of a uniformly labeled band occupying the area 1500-9000 A inside the axolemma. This region of the axon was rich in microtubules and organelles while the unlabeled central core of the axon contained mainly neurofilaments. This observation supports the hypothesis that microtubules are related to axonal transport. In small, vesicle-filled nerve terminals in the blastema, labeled material was restricted to a thin zone a short distance beneath the plasma membrane while the central region of the terminal was largely unlabeled. The peripheral pattern of labeling in the nerve endings is consistent with successive addition of newly synthesized proteins at the periphery of the growth cone and release of substances such as trophic factors at the nerve terminal.

摘要

将亮氨酸 -(3)H注入再生蝾螈的脊髓或感觉神经节后,通过电子显微镜放射自显影术确定其在神经元中的分布。注入后3天,在神经细胞体中,单位面积内标记物的最高浓度出现在糙面内质网上。在粗大的臂神经中,银颗粒在轴浆中分布不均匀,这表明标记物质在轴突内的移动受到限制,只能到达轴突的某些区域。在有髓神经中观察到的几乎所有放射自显影颗粒,都可归因于轴膜内1500 - 9000埃区域存在一条均匀标记的带。轴突的这个区域富含微管和细胞器,而轴突未标记的中央核心主要含有神经丝。这一观察结果支持了微管与轴突运输相关的假说。在胚基中充满小泡的小神经末梢内,标记物质被限制在质膜下方短距离处的一个薄区域内,而末梢的中央区域基本未被标记。神经末梢中标记的外周模式与生长锥外周新合成蛋白质的连续添加以及神经末梢处营养因子等物质的释放相一致。

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