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少突胶质细胞中的整合素信号传导及其在中枢神经系统髓鞘形成中的重要性。

Integrin signaling in oligodendrocytes and its importance in CNS myelination.

作者信息

O'Meara Ryan W, Michalski John-Paul, Kothary Rashmi

机构信息

Regenerative Medicine Program, Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, ON, Canada K1H 8L6.

出版信息

J Signal Transduct. 2011;2011:354091. doi: 10.1155/2011/354091. Epub 2010 Dec 20.

Abstract

Multiple sclerosis is characterized by repeated demyelinating attacks of the central nervous system (CNS) white matter tracts. To tailor novel therapeutics to halt or reverse disease process, we require a better understanding of oligodendrocyte biology and of the molecular mechanisms that initiate myelination. Cell extrinsic mechanisms regulate CNS myelination through the interaction of extracellular matrix proteins and their transmembrane receptors. The engagement of one such receptor family, the integrins, initiates intracellular signaling cascades that lead to changes in cell phenotype. Oligodendrocytes express a diverse array of integrins, and the expression of these receptors is developmentally regulated. Integrin-mediated signaling is crucial to the proliferation, survival, and maturation of oligodendrocytes through the activation of downstream signaling pathways involved in cytoskeletal remodeling. Here, we review the current understanding of this important signaling axis and its role in oligodendrocyte biology and ultimately in the myelination of axons within the CNS.

摘要

多发性硬化症的特征是中枢神经系统(CNS)白质束反复发生脱髓鞘发作。为了定制新的疗法以阻止或逆转疾病进程,我们需要更好地了解少突胶质细胞生物学以及启动髓鞘形成的分子机制。细胞外机制通过细胞外基质蛋白与其跨膜受体的相互作用来调节中枢神经系统的髓鞘形成。其中一个受体家族——整合素的结合会启动细胞内信号级联反应,导致细胞表型发生变化。少突胶质细胞表达多种整合素,并且这些受体的表达受发育调控。整合素介导的信号传导通过激活参与细胞骨架重塑的下游信号通路,对少突胶质细胞的增殖、存活和成熟至关重要。在这里,我们综述了对这一重要信号轴的当前认识及其在少突胶质细胞生物学中的作用,并最终在中枢神经系统轴突的髓鞘形成中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acab/3101883/5e2b1b1ac196/JST2011-354091.001.jpg

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