Costa Carme, Tortosa Raül, Rodríguez Agustín, Ferrer Isidre, Torres Juan Maria, Bassols Anna, Pumarola Martí
Departament de Medicina i Cirurgia Animals, Universitat Autònoma de Barcelona, 08193 Bellaterra (Cerdanyola del Vallès), Barcelona, Spain.
Brain Res. 2007 Oct 17;1175:96-106. doi: 10.1016/j.brainres.2007.06.088. Epub 2007 Jul 27.
Aquaporins (AQP) are a family of transmembrane proteins that act as water selective channels. AQP1 and AQP4 are widely expressed in the central nervous system where they play several roles. Overexpression of AQP has been reported in some human and animal transmissible spongiform encephalopathies, but information is scanty about their distribution in the central nervous system in bovine spongiform encephalopathy (BSE). Double immunohistochemistry for AQP1, AQP4 and GFAP was developed in a transgenic mouse line overexpressing the bovine cellular prion protein (BoTg110), intracerebrally infected with cattle BSE. Western blot for AQP1 and AQP4, and immunohistochemistry for both AQP and GFAP were carried out in cases of BSE-diagnosed cattle as part of surveillance plan in Catalonia (Spain). A marked increase in AQP1 and AQP4 was observed in mice at the terminal stage of the disease, when they had a wide range of clinical signs, whereas no increase could be observed in the early stage before the onset of the clinical signs. In cattle which did not show evidence of clinical signs, both AQP already showed a great increase. The AQP overexpression correlated with GFAP-immunoreactive astrocytes and PrPres deposition in both cases. The results of this study suggest that AQP overexpression in glial cells could lead to an imbalance in water and ion homeostasis which could contribute to triggering the typical histopathological changes of BSE.
水通道蛋白(AQP)是一类跨膜蛋白家族,作为水选择性通道发挥作用。AQP1和AQP4在中枢神经系统中广泛表达,在其中发挥多种作用。在一些人类和动物的传染性海绵状脑病中已报道了AQP的过表达,但关于它们在牛海绵状脑病(BSE)中枢神经系统中的分布信息却很少。在一种过表达牛细胞朊蛋白(BoTg110)并经脑内接种牛BSE感染的转基因小鼠品系中,开展了AQP1、AQP4和胶质纤维酸性蛋白(GFAP)的双重免疫组织化学研究。作为西班牙加泰罗尼亚监测计划的一部分,对经BSE诊断的牛进行了AQP1和AQP4的蛋白质印迹分析以及AQP和GFAP的免疫组织化学分析。在疾病终末期出现广泛临床症状的小鼠中观察到AQP1和AQP4显著增加,而在临床症状出现前的早期阶段未观察到增加。在未表现出临床症状迹象的牛中,两种AQP已经显示出大幅增加。在这两种情况下,AQP的过表达均与GFAP免疫反应性星形胶质细胞和蛋白酶抗性朊蛋白(PrPres)沉积相关。本研究结果表明,胶质细胞中AQP的过表达可能导致水和离子稳态失衡,这可能有助于引发BSE典型的组织病理学变化。