Department of Internal Medicine, Washington University in St. Louis, St. Louis, MO 63110.
Department of Physiology, University of Kiel, 24118 Kiel, Germany.
Proc Natl Acad Sci U S A. 2017 May 16;114(20):5271-5276. doi: 10.1073/pnas.1701006114. Epub 2017 May 1.
Whether the tight junction is permeable to water remains highly controversial. Here, we provide evidence that the tricellular tight junction is important for paracellular water permeation and that Ig-like domain containing receptor 1 (ILDR1) regulates its permeability. In the mouse kidney, ILDR1 is localized to tricellular tight junctions of the distal tubules. Genetic knockout of in the mouse kidney causes polyuria and polydipsia due to renal concentrating defects. Microperfusion of live renal distal tubules reveals that they are impermeable to water in normal animals but become highly permeable to water in knockout animals whereas paracellular ionic permeabilities in the knockout mouse renal tubules are not affected. Vasopressin cannot correct paracellular water loss in knockout animals despite normal effects on the transcellular aquaporin-2-dependent pathway. In cultured renal epithelial cells normally lacking the expression of , overexpression of significantly reduces the paracellular water permeability. Together, our study provides a mechanism of how cells transport water and shows how such a mechanism may be exploited as a therapeutic approach to maintain water homeostasis.
紧密连接是否允许水通过仍然存在很大争议。在这里,我们提供的证据表明,三细胞紧密连接对于细胞旁水渗透很重要,并且免疫球蛋白样结构域包含受体 1(ILDR1)调节其渗透性。在小鼠肾脏中,ILDR1 定位于远端肾小管的三细胞紧密连接。在小鼠肾脏中敲除 会导致多尿和多饮,这是由于肾脏浓缩功能缺陷所致。对活体肾远端小管的微灌注显示,在正常动物中它们对水不可渗透,但在 敲除动物中变得高度可渗透,而 敲除小鼠肾小管中的细胞旁离子渗透性不受影响。尽管血管加压素对细胞间水通道蛋白-2 依赖性途径有正常作用,但不能纠正 敲除动物的细胞旁水丢失。在正常情况下缺乏表达的培养的肾上皮细胞中,过表达 显著降低了细胞旁水通透性。总之,我们的研究提供了细胞如何运输水的机制,并表明这种机制如何被用作维持水稳态的治疗方法。