生长锥引导和轴突分支的共同机制。

Journal of neurobiology Pub Date : 2000-08-01
K Kalil, G Szebenyi, E W Dent
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引用次数: 0

摘要

在发育过程中,生长锥将生长轴突导向合适的目标。然而,在一些皮层通路中,目标神经支配通过侧枝的发育发生,侧枝从轴突轴向间质延伸。这些分支是如何形成的?活体脑皮层切片的直接观察表明,胼胝体轴突的生长锥在其皮层目标下暂停数小时,然后才发育成间质分支。对游离的活皮层神经元进行长时间的高分辨率成像显示,生长锥通过长时间的暂停行为和生长锥的扩大来划定未来轴突分支的位置。在新的生长锥形成并继续向前推进后,大生长锥的丝状和板状残余物被留在轴突轴上,间隙分支随后由此产生。为了研究细胞骨架是如何在轴突分支点重组的,我们荧光标记了活皮层神经元中的微管,并对微管在轴突轴和生长锥新生长过程中的行为进行了成像。在这两个区域,微管通过散开和分裂重组成更具可塑性的形式。这些较短的微管然后以顺行和逆行的运动侵入新发育的分支。尽管游离皮质神经元的轴突分支发生在没有靶标的情况下,靶标衍生生长因子FGF-2的应用大大增强了分支。综上所述,这些结果表明生长锥暂停与轴突分支密切相关,并表明从末端生长锥和轴突轴向轴突生长的共同机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Common mechanisms underlying growth cone guidance and axon branching.

During development, growth cones direct growing axons into appropriate targets. However, in some cortical pathways target innervation occurs through the development of collateral branches that extend interstitially from the axon shaft. How do such branches form? Direct observations of living cortical brain slices revealed that growth cones of callosal axons pause for many hours beneath their cortical targets prior to the development of interstitial branches. High resolution imaging of dissociated living cortical neurons for many hours revealed that the growth cone demarcates sites of future axon branching by lengthy pausing behaviors and enlargement of the growth cone. After a new growth cone forms and resumes forward advance, filopodial and lamellipodial remnants of the large paused growth cone are left behind on the axon shaft from which interstitial branches later emerge. To investigate how the cytoskeleton reorganizes at axon branch points, we fluorescently labeled microtubules in living cortical neurons and imaged the behaviors of microtubules during new growth from the axon shaft and the growth cone. In both regions microtubules reorganize into a more plastic form by splaying apart and fragmenting. These shorter microtubules then invade newly developing branches with anterograde and retrograde movements. Although axon branching of dissociated cortical neurons occurs in the absence of targets, application of a target-derived growth factor, FGF-2, greatly enhances branching. Taken together, these results demonstrate that growth cone pausing is closely related to axon branching and suggest that common mechanisms underlie directed axon growth from the terminal growth cone and the axon shaft.

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