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少突胶质细胞中细胞骨架的组织及功能作用

Organization and functional roles of the cytoskeleton in oligodendrocytes.

作者信息

Richter-Landsberg C

机构信息

Department of Biology, Molecular Neurobiology, University of Oldenburg, POB 2503, D-26111 Oldenburg, Germany.

出版信息

Microsc Res Tech. 2001 Mar 15;52(6):628-36. doi: 10.1002/jemt.1047.

DOI:10.1002/jemt.1047
PMID:11276115
Abstract

Mature oligodendrocytes are characterized by their numerous cytoplasmic extensions and flat membranous sheets. These sheets contain an extensive cytoskeletal network of microtubules (MTs) that maintain the cellular morphology, are specifically important for cellular sorting, and provide the rails for organelle trafficking. Mitochondria are localized in the primary and secondary processes and follow the tracks of the MTs in the cytoplasmic extensions. Oligodendrocytes express microtubule associated proteins (MAPs), specifically MAP2 and tau, which might be involved in the regulation and stabilization of the dynamic MT network in the myelin-containing cellular processes. Tau and MAP2 heterogeneity increases during oligodendroglia maturation, and in mature oligodendrocytes tau mRNA with four MT binding domains are more prominent than in progenitor cells. Filamentous cell inclusions are a unifying mechanism underlying a variety of late-onset neurodegenerative disorders and have mainly been viewed as neuron-specific. Recent evidence indicated that glial changes occur in CNS degenerative diseases and seem to be a more common feature than previously thought. Glial fibrillary tangles (GFTs) in oligodendrocytes were observed in familial multiple system tauopathy, and glial cytoplasmic inclusions (GCIs) and oligodendroglia degeneration are the histological hallmark of multiple system atrophy (MSA). GCIs are associated with MTs and contain stress proteins and MAPs. Thus, neurons and glial cells share common cytoskeletal pathologies. During health and disease, MAPs might be important regulators of the structural stability and plasticity of the oligodendroglia cytoskeleton.

摘要

成熟少突胶质细胞的特征是具有众多的细胞质延伸和扁平的膜状薄片。这些薄片包含广泛的微管(MTs)细胞骨架网络,该网络维持细胞形态,对细胞分选尤为重要,并为细胞器运输提供轨道。线粒体定位于初级和次级突起中,并沿着细胞质延伸中的微管轨迹移动。少突胶质细胞表达微管相关蛋白(MAPs),特别是MAP2和tau,它们可能参与含髓鞘细胞突起中动态微管网络的调节和稳定。在少突胶质细胞成熟过程中,tau和MAP2的异质性增加,并且在成熟少突胶质细胞中,具有四个微管结合结构域的tau mRNA比祖细胞中更突出。丝状细胞内含物是多种迟发性神经退行性疾病的统一机制,主要被视为神经元特异性的。最近的证据表明,中枢神经系统退行性疾病中会发生胶质细胞变化,而且这似乎是比以前认为的更常见的特征。在家族性多系统tau病中观察到少突胶质细胞中的胶质原纤维缠结(GFTs),而胶质细胞质内含物(GCIs)和少突胶质细胞变性是多系统萎缩(MSA)的组织学标志。GCIs与微管相关,包含应激蛋白和MAPs。因此,神经元和胶质细胞共享共同的细胞骨架病理学。在健康和疾病状态下,MAPs可能是少突胶质细胞骨架结构稳定性和可塑性的重要调节因子。

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