Institute of Biomedicine of Seville (IBiS), Virgen del Rocío University Hospital, (HUVR)/Spanish National Research Council (CSIC)/University of Seville, 41013 Seville, Spain.
Department of Physiology and Biophysics, University of Seville, 41009 Seville, Spain.
Biomolecules. 2022 Mar 31;12(4):530. doi: 10.3390/biom12040530.
Brain aquaporins facilitate the movement of water between the four water compartments: blood, cerebrospinal fluid, interstitial fluid, and intracellular fluid. This work analyzes the expression of the four most abundant aquaporins (AQPs) (AQP1, AQP4, AQP9, and AQP11) in the brains of mice and discuss their contribution to hydrocephalus. We analyzed available data from single-cell RNA sequencing of the central nervous system of mice to describe the expression of aquaporins and compare their distribution with that based on qPCR, western blot, and immunohistochemistry assays. Expression of AQP1 in the apical cell membrane of choroid plexus epithelial cells and of AQP4 in ependymal cells, glia limitans, and astrocyte processes in the pericapillary end foot is consistent with the involvement of both proteins in cerebrospinal fluid homeostasis. The expression of both aquaporins compensates for experimentally induced hydrocephalus in the animals. Recent data demonstrate that hypoxia in aged animals alters AQP4 expression in the choroidal plexus and cortex, increasing the ventricle size and intraventricular pressure. Cerebral distensibility is reduced in parallel with a reduction in cerebrospinal fluid drainage and cognitive deterioration. We propose that aged mice chronically exposed to hypoxia represent an excellent experimental model for studying the pathophysiological characteristics of idiopathic normal pressure hydrocephalus and roles for AQPs in such disease.
脑水通道蛋白促进四个水隔室(血液、脑脊液、细胞间质液和细胞内液)之间的水移动。这项工作分析了在小鼠脑中最丰富的四种水通道蛋白(AQP1、AQP4、AQP9 和 AQP11)的表达,并讨论了它们对脑积水的贡献。我们分析了来自小鼠中枢神经系统单细胞 RNA 测序的可用数据,以描述水通道蛋白的表达,并将其分布与基于 qPCR、western blot 和免疫组织化学检测的分布进行比较。脉络丛上皮细胞顶膜上的 AQP1 和室管膜细胞、胶质界膜和血管周足星形胶质细胞突起中的 AQP4 的表达与这两种蛋白参与脑脊液稳态一致。这两种水通道蛋白的表达都能补偿动物实验性诱导的脑积水。最近的数据表明,老年动物中的缺氧会改变脉络丛和皮质中的 AQP4 表达,增加脑室大小和颅内压。脑顺应性与脑脊液引流减少和认知恶化平行降低。我们提出,长期暴露于缺氧的老年小鼠代表了研究特发性正常压力脑积水的病理生理特征以及 AQP 在这种疾病中的作用的理想实验模型。