Center of Excellence for Aging & Brain Repair, University of South Florida, Morsani College of Medicine, Tampa, Florida, USA.
Int Rev Neurobiol. 2012;102:91-106. doi: 10.1016/B978-0-12-386986-9.00004-1.
Amyotrophic lateral sclerosis (ALS) is a severe neurodegenerative disease with a complicated and poorly understood pathogenesis. Strong evidence indicates impairment of all neurovascular unit components including the blood-brain and blood-spinal cord barriers (BBB/BSCB) in both patients and animal models. The present review provides an updated analysis of the microvascular pathology and impaired BBB/BSCB in ALS. Based on experimental and clinical ALS studies, the roles of cellular components, cell interactions, tight junctions, transport systems, cytokines, matrix metalloproteinases, and free radicals in the BBB/BSCB disruption are discussed. The impact of BBB/BSCB damage in ALS pathogenesis is a novel research topic, and this review will reveal some aspects of microvascular pathology involved in the disease and hopefully engender new therapeutic approaches.
肌萎缩侧索硬化症(ALS)是一种严重的神经退行性疾病,其发病机制复杂且尚未完全阐明。大量证据表明,患者和动物模型的所有神经血管单元成分(包括血脑和血脊髓屏障(BBB/BSCB))都受到损害。本综述提供了对 ALS 中小血管病理学和受损 BBB/BSCB 的最新分析。基于实验和临床 ALS 研究,讨论了细胞成分、细胞相互作用、紧密连接、转运系统、细胞因子、基质金属蛋白酶和自由基在 BBB/BSCB 破坏中的作用。BBB/BSCB 损伤在 ALS 发病机制中的作用是一个新的研究课题,本综述将揭示疾病中涉及的微血管病理学的一些方面,并有望产生新的治疗方法。