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Rapid changes in the distribution of GAP-43 correlate with the expression of neuronal polarity during normal development and under experimental conditions

机译:在正常发育和实验条件下GAP-43分布的快速变化与神经元极性的表达相关

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摘要

Hippocampal neurons growing in culture initially extend several, short minor processes that have the potential to become either axons or dendrites. The first expression of polarity occurs when one of these minor processes begins to elongate rapidly, becoming the axon. Before axonal outgrowth, the growth-associated protein GAP-43 is distributed equally among the growth cones of the minor processes; it is preferentially concentrated in the axonal growth cone once polarity has been established (Goslin, K., D. Schreyer, J. Skene, and G. Banker. 1990. J. Neurosci. 10:588-602). To determine when the selective segregation of GAP-43 begins, we followed individual cells by video microscopy, fixed them as soon as the axon could be distinguished, and localized GAP-43 by immunofluorescence microscopy. Individual minor processes acquired axonal growth characteristics within a period of 30- 60 min, and GAP-43 became selectively concentrated to the growth cones of these processes with an equally rapid time course. We also examined changes in the distribution of GAP-43 after transection of the axon. After an axonal transection that is distant from the soma, neuronal polarity is maintained, and the original axon begins to regrow almost immediately. In such cases, GAP-43 became selectively concentrated in the new axonal growth cone within 12-30 min. In contrast, when the axon is transected close to the soma, polarity is lost; the original axon rarely regrows, and there is a significant delay before a new axon emerges. Under these circumstances, GAP-43 accumulated in the new growth cone much more slowly, suggesting that its ongoing selective routing to the axon had been disrupted by the transection. These results demonstrate that the selective segregation of GAP-43 to the growth cone of a single process is closely correlated with the acquisition of axonal growth characteristics and, hence, with the expression of polarity.
机译:在培养物中生长的海马神经元最初会延伸几个短的微小过程,这些过程可能会变成轴突或树突。当这些次要过程中的一个开始迅速伸长并变成轴突时,就会出现极性的第一个表达。在轴突生长之前,与生长相关的蛋白质GAP-43在各个小突起的生长锥之间平均分布。一旦建立了极性,它优先集中在轴突生长锥中(Goslin,K.,D.Schreyer,J.Skene,和G.Banker.1990.J.Neurosci.10:588-602)。为了确定GAP-43的选择性分离何时开始,我们通过视频显微镜观察了单个细胞,一旦轴突得以区分就将其固定,并通过免疫荧光显微镜术定位了GAP-43。单个较小的过程在30-60分钟内获得了轴突的生长特征,并且GAP-43在同样快速的过程中选择性地集中于这些过程的生长锥。我们还检查了轴突横断后GAP-43的分布变化。在远离躯干的轴突横切后,神经元的极性得以维持,原始的轴突几乎立即开始再生长。在这种情况下,GAP-43在12-30分钟内选择性地集中在新的轴突生长锥中。相反,当轴突靠近躯干横切时,极性丧失;最初的轴突很少再生,并且在出现新轴突之前存在明显的延迟。在这种情况下,GAP-43在新生长锥中的积聚速度要慢得多,这表明其正在进行的选择性到达轴突的路径已被横断所破坏。这些结果表明,GAP-43选择性分离到单个过程的生长锥与轴突生长特征的获得并因此与极性的表达密切相关。

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