Deeg Cornelia A, Amann Barbara, Lutz Konstantin, Hirmer Sieglinde, Lutterberg Karina, Kremmer Elisabeth, Hauck Stefanie M
Experimental Ophthalmology, Philipps University of Marburg, Baldingerstrasse, 35033, Marburg, Germany.
Department of Veterinary Sciences, Institute of Animal Physiology, Ludwig-Maximilians University, Veterinärstr. 13, 80539, München, Germany.
J Neuroinflammation. 2016 Apr 23;13(1):89. doi: 10.1186/s12974-016-0554-2.
Müller glial cells are important regulators of physiological function of retina. In a model disease of retinal inflammation and spontaneous recurrent uveitis in horses (ERU), we could show that retinal Müller glial cells significantly change potassium and water channel protein expression during autoimmune pathogenesis. The most significantly changed channel protein in neuroinflammatory ERU was aquaporin 11 (AQP11). Aquaporins (AQP, 13 members) are important regulators of water and small solute transport through membranes. AQP11 is an unorthodox member of this family and was assigned to a third group of AQPs because of its difference in amino acid sequence (conserved sequence is only 11 %) and especially its largely unknown function.
In order to gain insight into the distribution, localization, and function of AQP11 in the retina, we first developed a novel monoclonal antibody for AQP11 enabling quantification, localization, and functional studies.
In the horse retina, AQP11 was exclusively expressed at Müller glial cell membranes. In uveitic condition, AQP11 disappeared from gliotic Müller cells concomitant with glutamine synthase. Since function of AQP11 is still under debate, we assessed the impact of AQP11 channel on cell volume regulation of primary Müller glial cells under different osmotic conditions. We conclude a concomitant role for AQP11 with AQP4 in water efflux from these glial cells, which is disturbed in ERU. This could probably contribute to swelling and subsequent severe complication of retinal edema through impaired intracellular fluid regulation.
Therefore, AQP11 is important for physiological Müller glia function and the expression pattern and function of this water channel seems to have distinct functions in central nervous system. The significant reduction in neuroinflammation points to a crucial role in pathogenesis of autoimmune uveitis.
缪勒神经胶质细胞是视网膜生理功能的重要调节因子。在马的视网膜炎症和自发性复发性葡萄膜炎(ERU)这一模型疾病中,我们发现视网膜缪勒神经胶质细胞在自身免疫发病机制中会显著改变钾离子和水通道蛋白的表达。在神经炎性ERU中变化最显著的通道蛋白是水通道蛋白11(AQP11)。水通道蛋白(AQP,共13个成员)是水和小分子溶质跨膜运输的重要调节因子。AQP11是该家族的一个非传统成员,因其氨基酸序列差异(保守序列仅11%),尤其是其功能 largely未知,而被归为第三组水通道蛋白。
为深入了解AQP11在视网膜中的分布、定位和功能,我们首先开发了一种针对AQP11的新型单克隆抗体,用于定量、定位和功能研究。
在马视网膜中,AQP11仅在缪勒神经胶质细胞膜上表达。在葡萄膜炎状态下,AQP11与谷氨酰胺合成酶一起从胶质化的缪勒细胞中消失。由于AQP11的功能仍存在争议,我们评估了AQP11通道在不同渗透条件下对原代缪勒神经胶质细胞体积调节的影响。我们得出结论,AQP11与AQP4在这些神经胶质细胞的水流出过程中具有协同作用,而这一过程在ERU中受到干扰。这可能通过细胞内液调节受损导致视网膜水肿肿胀及随后的严重并发症。
因此,AQP11对缪勒神经胶质细胞的生理功能很重要,这种水通道的表达模式和功能在中枢神经系统似乎具有独特作用。神经炎症中其显著减少表明它在自身免疫性葡萄膜炎发病机制中起关键作用。