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轴突侧支分支的细胞骨架和信号机制。

The cytoskeletal and signaling mechanisms of axon collateral branching.

机构信息

Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, Pennsylvania 19129, USA.

出版信息

Dev Neurobiol. 2011 Mar;71(3):201-20. doi: 10.1002/dneu.20852.

Abstract

During development, axons are guided to their appropriate targets by a variety of guidance factors. On arriving at their synaptic targets, or while en route, axons form branches. Branches generated de novo from the main axon are termed collateral branches. The generation of axon collateral branches allows individual neurons to make contacts with multiple neurons within a target and with multiple targets. In the adult nervous system, the formation of axon collateral branches is associated with injury and disease states and may contribute to normally occurring plasticity. Collateral branches are initiated by actin filament– based axonal protrusions that subsequently become invaded by microtubules, thereby allowing the branch to mature and continue extending. This article reviews the current knowledge of the cellular mechanisms of the formation of axon collateral branches. The major conclusions of this review are (1) the mechanisms of axon extension and branching are not identical; (2) active suppression of protrusive activity along the axon negatively regulates branching; (3) the earliest steps in the formation of axon branches involve focal activation of signaling pathways within axons, which in turn drive the formation of actin-based protrusions; and (4) regulation of the microtubule array by microtubule-associated and severing proteins underlies the development of branches. Linking the activation of signaling pathways to specific proteins that directly regulate the axonal cytoskeleton underlying the formation of collateral branches remains a frontier in the field.

摘要

在发育过程中,轴突通过多种导向因子被导向其适当的靶标。到达突触靶标或在途中,轴突形成分支。从主轴突新生成的分支称为侧支分支。轴突侧支分支的产生允许单个神经元与靶标内的多个神经元以及多个靶标建立联系。在成年神经系统中,轴突侧支分支的形成与损伤和疾病状态有关,可能有助于正常发生的可塑性。侧支分支由肌动蛋白丝为基础的轴突突起引发,随后微管侵入其中,从而允许分支成熟并继续延伸。本文综述了轴突侧支分支形成的细胞机制的现有知识。这篇综述的主要结论是:(1) 轴突延伸和分支的机制并不相同;(2) 主动抑制轴突上的突起活动会负向调节分支;(3) 轴突分支形成的早期步骤涉及轴突内信号通路的焦点激活,进而驱动肌动蛋白突起的形成;(4) 微管相关蛋白和切断蛋白对微管阵列的调节是分支发育的基础。将信号通路的激活与直接调节侧支分支形成的轴突细胞骨架的特定蛋白联系起来仍然是该领域的一个前沿。

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