Saadoun S, Tait M J, Reza A, Davies D Ceri, Bell B A, Verkman A S, Papadopoulos M C
Academic Neurosurgery Unit, St. George's, University of London, London, UK.
Neuroscience. 2009 Jul 7;161(3):764-72. doi: 10.1016/j.neuroscience.2009.03.069. Epub 2009 Apr 5.
The glial cell water channel aquaporin-4 (AQP4) plays an important role in brain edema, astrocyte migration, and neuronal excitability. Zhou et al. [Zhou J, Kong H, Hua X, Xiao M, Ding J, Hu G (2008) Altered blood-brain barrier integrity in adult aquaporin-4 knockout mice. Neuroreport 19:1-5] recently reported that AQP4 deletion significantly altered blood-brain barrier integrity and glial fibrillary acidic protein (GFAP) immunoreactivity in their AQP4 null mice. Here we describe a detailed characterization of baseline brain properties in our AQP4 null mice, including gross appearance, neuronal, astrocyte and oligodendrocyte characteristics, and blood-brain barrier integrity. Gross anatomical measurements included estimates of brain and ventricle size. Neurons, astrocytes and oligodendrocytes were assessed using the neuronal nuclear marker NeuN, the astrocyte marker GFAP, and the myelin stain Luxol Fast Blue. The blood-brain barrier was studied by electron microscopy and the horseradish peroxidase extravasation technique. There were no differences in brain and ventricle sizes between wild type and AQP4 null mice, nor were there differences in the cerebral cortical density of NeuN positive nuclei, perimicrovessel and glia limitans GFAP immunoreactivity, or the thickness and myelination of the corpus callosum. The ultrastructure of microvessels in the frontal cortex and caudate nucleus of wild type vs. AQP4 null mice was indistinguishable, with features including intact endothelial tight junctions, absence of perimicrovessel astrocyte foot process edema, and absence of horseradish peroxidase extravasation. In contrast to the report by Zhou et al. (2008), our data show that AQP4 deletion in mice does not produce major structural abnormalities in the brain.
胶质细胞水通道水通道蛋白4(AQP4)在脑水肿、星形胶质细胞迁移和神经元兴奋性中起重要作用。周等人[周J,孔H,华X,肖M,丁J,胡G(2008年)成年水通道蛋白4基因敲除小鼠血脑屏障完整性的改变。神经报告19:1 - 5]最近报道,在他们的AQP4基因敲除小鼠中,AQP4缺失显著改变了血脑屏障完整性和胶质纤维酸性蛋白(GFAP)免疫反应性。在此,我们描述了我们的AQP4基因敲除小鼠基线脑特性的详细特征,包括大体外观、神经元、星形胶质细胞和少突胶质细胞特征以及血脑屏障完整性。大体解剖测量包括脑和脑室大小的估计。使用神经元核标记物NeuN、星形胶质细胞标记物GFAP和髓磷脂染色剂Luxol Fast Blue对神经元、星形胶质细胞和少突胶质细胞进行评估。通过电子显微镜和辣根过氧化物酶外渗技术研究血脑屏障。野生型和AQP4基因敲除小鼠之间的脑和脑室大小没有差异,NeuN阳性核的大脑皮质密度、微血管周围和胶质界膜GFAP免疫反应性或胼胝体的厚度和髓鞘形成也没有差异。野生型与AQP4基因敲除小鼠额叶皮质和尾状核微血管的超微结构没有区别,其特征包括完整的内皮紧密连接、微血管周围星形胶质细胞足突水肿的缺失以及辣根过氧化物酶外渗的缺失。与周等人(2008年)的报告相反,我们的数据表明,小鼠中的AQP4缺失不会在脑中产生主要的结构异常。