Hsu Ying, Tran Minh, Linninger Andreas A
Andreas Linninger, 851 S Morgan St., SEO 218, MC 063, Chicago, IL 60607, USA,
Croat Med J. 2015 Oct;56(5):401-21. doi: 10.3325/cmj.2015.56.401.
Aquaporin-4 water channels play a central role in brain water regulation in neurological disorders. Aquaporin-4 is abundantly expressed at the astroglial endfeet facing the cerebral vasculature and the pial membrane, and both its expression level and subcellular localization significantly influence brain water transport. However, measurements of aquaporin-4 levels in animal models of brain injury often report opposite trends of change at the injury core and the penumbra. Furthermore, aquaporin-4 channels play a beneficial role in brain water clearance in vasogenic edema, but a detrimental role in cytotoxic edema and exacerbate cell swelling. In light of current evidence, we still do not have a complete understanding of the role of aquaporin-4 in brain water transport. In this review, we propose that the regulatory mechanisms of aquaporin-4 at the transcriptional, translational, and post-translational levels jointly regulate water permeability in the short and long time scale after injury. Furthermore, in order to understand why aquaporin-4 channels play opposing roles in cytotoxic and vasogenic edema, we discuss experimental evidence on the dynamically changing osmotic gradients between blood, extracellular space, and the cytosol during the formation of cytotoxic and vasogenic edema. We conclude with an emerging picture of the distinct osmotic environments in cytotoxic and vasogenic edema, and propose that the directions of aquaporin-4-mediated water clearance in these two types of edema are distinct. The difference in water clearance pathways may provide an explanation for the conflicting observations of the roles of aquaporin-4 in edema resolution.
水通道蛋白4水通道在神经系统疾病的脑水调节中起核心作用。水通道蛋白4大量表达于面向脑血管和软脑膜的星形胶质细胞终足,其表达水平和亚细胞定位均显著影响脑水运输。然而,在脑损伤动物模型中测量水通道蛋白4水平时,常常报告损伤核心区和半暗带的变化趋势相反。此外,水通道蛋白4通道在血管源性水肿的脑水清除中起有益作用,但在细胞毒性水肿中起有害作用并加剧细胞肿胀。鉴于目前的证据,我们对水通道蛋白4在脑水运输中的作用仍未完全了解。在本综述中,我们提出水通道蛋白4在转录、翻译和翻译后水平的调节机制共同调节损伤后短期和长期的水通透性。此外,为了理解为什么水通道蛋白4通道在细胞毒性水肿和血管源性水肿中起相反作用,我们讨论了细胞毒性水肿和血管源性水肿形成过程中血液、细胞外间隙和细胞质之间动态变化的渗透梯度的实验证据。我们以细胞毒性水肿和血管源性水肿中不同渗透环境的新情况作为结论,并提出这两种类型水肿中由水通道蛋白4介导的水清除方向是不同的。水清除途径的差异可能为水通道蛋白4在水肿消退中作用的矛盾观察结果提供一种解释。