发育和再生过程中神经元形状的控制。

M J Cohen, G F Hall
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引用次数: 8

摘要

我们研究了海七鳃鳗幼体中枢神经系统中穆勒网状脊髓神经元在轴突和树突损伤后发芽的能力。如果轴突切除发生在脊髓中远离体细胞的部位,则轴突残端会产生再生芽。然而,在靠近胞体的后脑部位进行轴切开术会导致大量的神经鞘从树突中萌发。这些“树突”芽的大体形态和轨迹类似于再生的轴突。切除穆勒细胞树突(树突切开术)而不进行轴突切开术,不会导致轴突或树突的神经鞘萌发,这表明萌发的发生特别需要轴突切开术。然而,树突切开术能够通过在树突切开术病变部位诱导发芽来改变先前被切开的穆勒细胞的发芽分布。树突状和轴突起源的芽都倾向于沿着或靠近后脑腹面沿线性、向东方向生长。一些芽在边缘表面形成非常大的棕榈状生长球果,这反过来又产生了许多分支,这些分支沿着大脑表面继续生长。我们讨论了在穆勒神经元的轴突切断后,树突和轴突的萌芽都是胚胎发生过程中轴突初始发育的再现,它们的轨迹是由持续存在于后脑腹侧的发育引导信号决定的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Control of neuron shape during development and regeneration.

We have examined the ability of Mueller reticulospinal neurons in the CNS of the larval sea lamprey to sprout following axonal and dendritic injury. Axotomy induces regenerative sprouting exclusively from the axon stump if it occurs at a site distant from the soma in the spinal cord. However, axotomy within the hindbrain at a site close to the soma results in profuse neuritic sprouting from the dendrites. The gross morphology and trajectories of these "dendritic" sprouts resemble those of regenerating axons. Amputation of Mueller cell dendrites (dendrotomy) without axotomy does not result in neuritic sprouting from either the axon or dendrites, indicating that axotomy is specifically required for sprouting to occur. However, dendrotomy is capable of altering the distribution of sprouting in a previously axotomized Mueller cell by inducing sprouting at the site of the dendrotomy lesion. Sprouts of both dendritic and axonal origin tend to follow linear, rostrocaudally oriented paths along or near the ventral surface of the hindbrain. Some sprouts form very large, palmate growth cones on the marginal surface, which in turn give rise to many branches that continue to grow either rostrally or caudally along the surface of the brain. We discuss the possibility that both dendritic and axonal sprouts evoked by axotomy of Mueller neurons are recapitulating initial axonal development during embryogenesis, and that their trajectories are determined by developmental guidance cues persisting in the ventral hindbrain.

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