Gundersen Georg Andreas, Vindedal Gry Fluge, Skare Oivind, Nagelhus Erlend A
Centre for Molecular Medicine Norway, Nordic EMBL Partnership, University of Oslo, P.O. Box 1137, Blindern, 0318, Oslo, Norway.
Brain Struct Funct. 2014 Nov;219(6):2181-6. doi: 10.1007/s00429-013-0629-0. Epub 2013 Aug 28.
Aquaporin-4 (AQP4) water channels are concentrated in astrocytic endfoot membranes at the brain-blood and brain-cerebrospinal fluid interfaces. The mechanisms underpinning the polarized distribution of AQP4 are poorly understood. Here we tested the hypothesis that pericytes regulate AQP4 anchoring to perivascular astrocytic endfoot membranes. AQP4 immunofluorescence of brain sections obtained from novel transgenic double reporter mice expressing enhanced green fluorescent protein (eGFP) in astrocytes and Discoma Red (DsRed) in pericytes revealed strong AQP4 signal in astrocytic processes adjacent to pericytes. Quantitative immunogold analysis of C57BL/6 mice showed that the AQP4 expression was higher in endfoot membranes abutting pericytes than in those facing endothelial cells. Similar findings were made for α-syntrophin, a member of the dystrophin-associated protein complex (DAPC). The enrichment of α-syntrophin in membranes ensheathing pericytes persisted after Aqp4 gene deletion. Our data support the concept that pericytes regulate AQP4 polarization.
水通道蛋白4(AQP4)水通道集中在脑血和脑脑脊液界面的星形胶质细胞终足膜中。支撑AQP4极化分布的机制尚不清楚。在这里,我们测试了一个假设,即周细胞调节AQP4锚定到血管周围星形胶质细胞终足膜上。从在星形胶质细胞中表达增强型绿色荧光蛋白(eGFP)和在周细胞中表达盘基网柄菌红色荧光蛋白(DsRed)的新型转基因双报告小鼠获得的脑切片的AQP4免疫荧光显示,在与周细胞相邻的星形胶质细胞突起中有强烈的AQP4信号。对C57BL/6小鼠的定量免疫金分析表明,与周细胞相邻的终足膜中AQP4的表达高于与内皮细胞相邻的终足膜。对于肌营养不良蛋白相关蛋白复合体(DAPC)的成员α-肌营养不良蛋白聚糖也有类似的发现。在Aqp4基因缺失后,包绕周细胞的膜中α-肌营养不良蛋白聚糖的富集仍然存在。我们的数据支持周细胞调节AQP4极化的概念。