首页> 外文期刊>The anatomical record: advances in integrative anatomy and evolutionary biology >The relationship between aquaporin-4 expression and blood-brain and spinal cord barrier permeability following experimental autoimmune encephalomyelitis in the rat.
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The relationship between aquaporin-4 expression and blood-brain and spinal cord barrier permeability following experimental autoimmune encephalomyelitis in the rat.

机译:实验性自身免疫性脑脊髓炎后水通道蛋白4表达与血脑和脊髓屏障通透性的关系。

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摘要

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.
机译:水通道蛋白4(AQP4)是水通道蛋白,在微血管星形胶质细胞足突,胶质限脂和室管膜中枢神经系统中强烈表达。 AQP4的表达在血脑屏障和血脊髓屏障中最高,支持其在跨这些结构的物质运输中的关键功能。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的潜在作用。本研究的目的是检查实验性自身免疫性脑脊髓炎大鼠小脑和脊髓中AQP4蛋白的表达。通过蛋白质印迹分析,在实验性自身免疫性脑脊髓炎发展过程中,AQP4表达增加,并在实验性自身免疫性脑脊髓炎的神经系统症状发作(腰部增大)或高潮(小脑)达到高峰。小脑血脑屏障和腰椎扩张血脊髓屏障的渗透性也更快,更明显地增加,与AQP4表达一致,这通过增加伊文思蓝渗漏和减少紧密连接蛋白表达来体现。总之,水通道蛋白上调可能参与实验性自身免疫性脑脊髓炎的急性期炎症的发展,并且可能与中枢神经系统屏障功能的损害有关。

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