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神经突起始中的肌动蛋白和微管:微管相关蛋白是缺失的环节吗?

Actin and microtubules in neurite initiation: are MAPs the missing link?

作者信息

Dehmelt Leif, Halpain Shelley

机构信息

Department of Cell Biology and Institute for Childhood and Neglected Diseases, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.

出版信息

J Neurobiol. 2004 Jan;58(1):18-33. doi: 10.1002/neu.10284.

DOI:10.1002/neu.10284
PMID:14598367
Abstract

During neurite initiation microtubules align to form a tight bundle and actin filaments reorganize to produce a growth cone. The mechanisms that underlie these highly coordinated cytoskeletal rearrangements are not yet fully understood. Recently, various levels of coordination between the actin- and microtubule-based cytoskeletons have been observed during cellular migration and morphogenesis, processes that share some similarities to neurite initiation. Direct, physical association between both cytoskeletons has been suggested, because microtubules often preferentially grow along actin bundles and transiently target actin-rich adhesion complexes. We propose that such physical association might be involved in force-based interactions and spatial organization of the two networks during neurite initiation as well. In addition, many signaling cascades that affect actin filaments are also involved in the regulation of microtubule dynamics, and vice versa. Although several candidates for mediating these effects have been identified in non-neuronal cells, the general mechanism is still poorly understood. In neurons certain plakins and neuron-specific microtubule associated proteins (MAPs), like MAP1B and MAP2, which can bind to both microtubules and F-actin, are promising candidates to play key roles in the specific cytoskeletal rearrangements controlling the transition from an undifferentiated state to neurite-bearing morphology. Here we review the effects of MAPs on microtubules and actin, as well as the coordination of both cytoskeletons during neurite initiation.

摘要

在神经突起始过程中,微管排列形成紧密束状,肌动蛋白丝重新组织以产生生长锥。这些高度协调的细胞骨架重排背后的机制尚未完全了解。最近,在细胞迁移和形态发生过程中观察到基于肌动蛋白和微管的细胞骨架之间存在不同程度的协调,这些过程与神经突起始有一些相似之处。有人提出两种细胞骨架之间存在直接的物理关联,因为微管通常优先沿着肌动蛋白束生长,并短暂靶向富含肌动蛋白的粘附复合物。我们认为这种物理关联也可能参与神经突起始过程中两个网络基于力的相互作用和空间组织。此外,许多影响肌动蛋白丝的信号级联反应也参与微管动力学的调节,反之亦然。虽然在非神经元细胞中已鉴定出几种介导这些效应的候选物,但总体机制仍知之甚少。在神经元中,某些盘状蛋白和神经元特异性微管相关蛋白(MAPs),如MAP1B和MAP2,它们既能结合微管又能结合F-肌动蛋白,有望在控制从未分化状态到具有神经突形态的转变的特定细胞骨架重排中发挥关键作用。在这里,我们综述了MAPs对微管和肌动蛋白的影响,以及神经突起始过程中两种细胞骨架的协调。

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