Rosenzweig Shira, Carmichael S Thomas
Department of Neurology, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
Brain Res. 2015 Oct 14;1623:123-34. doi: 10.1016/j.brainres.2015.02.019. Epub 2015 Feb 20.
Approximately one quarter of all strokes in humans occur in white matter, and the progressive nature of white matter lesions often results in severe physical and mental disability. Unlike cortical grey matter stroke, the pathology of white matter stroke revolves around disrupted connectivity and injured axons and glial cells, rather than neuronal cell bodies. Consequently, the mechanisms behind ischemic damage to white matter elements, the regenerative responses of glial cells and their signaling pathways, all differ significantly from those in grey matter. Development of effective therapies for white matter stroke would require an enhanced understanding of the complex cellular and molecular interactions within the white matter, leading to the identification of new therapeutic targets. This review will address the unique properties of the axon-glia unit during white matter stroke, describe the challenging process of promoting effective white matter repair, and discuss recently-identified signaling pathways which may hold potential targets for repair in this disease. This article is part of a Special Issue entitled SI: Cell Interactions In Stroke.
人类所有中风病例中约有四分之一发生在白质,白质病变的渐进性往往会导致严重的身心残疾。与皮质灰质中风不同,白质中风的病理围绕着连接中断以及轴突和神经胶质细胞受损,而非神经元细胞体。因此,白质成分缺血性损伤背后的机制、神经胶质细胞的再生反应及其信号通路,均与灰质中的显著不同。开发针对白质中风的有效疗法需要增强对白质内复杂细胞和分子相互作用的理解,从而确定新的治疗靶点。本综述将阐述白质中风期间轴突-神经胶质单元的独特特性,描述促进有效白质修复的具有挑战性的过程,并讨论最近发现的可能为此病提供修复潜在靶点的信号通路。本文是名为“中风中的细胞相互作用”特刊的一部分。