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用于分析中风中少突胶质细胞病理生理学的实验模型。

Experimental models for analysis of oligodendrocyte pathophysiology in stroke.

作者信息

Arai Ken, Lo Eng H

机构信息

Neuroprotection Research Laboratory, Massachusetts General Hospital, Harvard Medical School, Charlestown, USA.

出版信息

Exp Transl Stroke Med. 2009 Oct 24;1:6. doi: 10.1186/2040-7378-1-6.

Abstract

White matter damage is a clinically important part of stroke. However, compared to the mechanisms of neuronal injury in gray matter, white matter pathophysiology remains relatively understudied and poorly understood. This mini-review aims at summarizing current knowledge on experimental systems for analyzing the role of white matter injury relevant to stroke. In vitro platforms comprise primary cultures of both mature oligodendrocytes (OLGs) as well as oligodendrocyte precursor cells (OPCs). Tissue platforms involve preparations of optic nerve systems. Whole-animal platforms comprise in vivo models of cerebral ischemia that attempt to target white matter brain areas. While there is no single perfect model system, the collection of these experimental approaches have recently allowed a better understanding of the molecular and cellular pathways underlying OLG/OPC damage and demyelination. A systematic utilization of these cell, tissue and whole-animal platforms may eventually lead us to discover new targets for treating white matter injury in stroke and other CNS disorders.

摘要

白质损伤是中风临床上的重要组成部分。然而,与灰质中神经元损伤的机制相比,白质病理生理学的研究相对较少,了解也不够深入。本综述旨在总结当前关于分析与中风相关的白质损伤作用的实验系统的知识。体外平台包括成熟少突胶质细胞(OLGs)和少突胶质前体细胞(OPCs)的原代培养。组织平台涉及视神经系统的制备。全动物平台包括试图靶向脑白质区域的脑缺血体内模型。虽然没有单一的完美模型系统,但最近这些实验方法的集合使我们能够更好地理解OLG/OPC损伤和脱髓鞘的分子和细胞途径。系统地利用这些细胞、组织和全动物平台最终可能会引导我们发现治疗中风和其他中枢神经系统疾病中白质损伤的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25a8/2820444/035da7a6cb39/2040-7378-1-6-1.jpg

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