Department of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.
Anat Rec (Hoboken). 2011 Jan;294(1):46-54. doi: 10.1002/ar.21286. Epub 2010 Nov 12.
Aquaporin 4(AQP4) is a water channel protein strongly expressed in the central nervous system in perimicrovessel astrocyte foot processes, the glia limitans, and ependyma. Expression of AQP4 is highest at the blood-brain barrier and blood-spinal cord barrier, supporting its critical function in material transport across these structures. Recently, presence of the anti-aquaporin-4 antibody in sera has been used as an important diagnostic tool for neuromyelitis optica, suggesting a potential role in central nervous system inflammation. The aim of the present study was to examine AQP4 protein expression in the cerebellum and spinal cord from rats with experimental autoimmune encephalomyelitis. By western blot analysis, AQP4 expression increased during experimental autoimmune encephalomyelitis development, and peaked at onset (lumbar enlargement) or climax (cerebellum) of neurological signs of experimental autoimmune encephalomyelitis. There was also a faster and more pronounced increase in permeability in the cerebellar blood-brain barrier and the lumbar enlargement blood-spinal cord barrier consistent with AQP4 expression, which was manifested by increased Evans Blue leakage and reduced tight junction protein expression. In conclusion, aquaporin upregulation may be involved in the development of inflammation in the acute phase of experimental autoimmune encephalomyelitis, and may correlate with damage to central nervous system barrier function.
水通道蛋白 4(AQP4)是一种在中枢神经系统中小血管周围星形胶质细胞足突、胶质界膜和室管膜强烈表达的水通道蛋白。AQP4 在血脑屏障和血脊髓屏障中的表达最高,支持其在这些结构中物质转运的关键功能。最近,血清中抗水通道蛋白 4 抗体的存在已被用作视神经脊髓炎的重要诊断工具,提示其在中枢神经系统炎症中可能发挥作用。本研究旨在研究实验性自身免疫性脑脊髓炎大鼠小脑和脊髓中的 AQP4 蛋白表达。通过 Western blot 分析,AQP4 表达在实验性自身免疫性脑脊髓炎发展过程中增加,并在实验性自身免疫性脑脊髓炎神经症状的发病(腰椎增大)或高峰(小脑)时达到峰值。小脑血脑屏障和腰椎增大血脊髓屏障的通透性也有更快和更明显的增加,与 AQP4 表达一致,这表现为 Evans Blue 渗漏增加和紧密连接蛋白表达减少。总之,水通道蛋白的上调可能参与了实验性自身免疫性脑脊髓炎急性期炎症的发展,并可能与中枢神经系统屏障功能的损伤相关。