Kawedia Jitesh D, Nieman Michelle L, Boivin Gregory P, Melvin James E, Kikuchi Ken-Ichiro, Hand Arthur R, Lorenz John N, Menon Anil G
Department of Molecular Genetics, University of Cincinnati College of Medicine, Cincinnati, OH 45267-0524, USA.
Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3621-6. doi: 10.1073/pnas.0608384104. Epub 2007 Feb 21.
To investigate potential physiological interactions between the transcellular and paracellular pathways of water transport, we asked whether targeted deletion of Aquaporin 5 (AQP5), the major transcellular water transporter in salivary acinar cells, affected paracellular transport of 4-kDa FITC-labeled dextran (FITC-D), which is transported through the paracellular but not the transcellular route. After i.v. injection of FITC-D into either AQP5 wild-type or AQP5-/- mice and saliva collection for fixed time intervals, we show that the relative amount of FITC-D transported in the saliva of AQP5-/- mice is half that in matched AQP5+/+ mice, indicating a 2-fold decrease in permeability of the paracellular barrier in mice lacking AQP5. We also found a significant difference in the proportion of transcellular vs. paracellular transport between male and female mice. Freeze-fracture electron microscopy revealed an increase in the number of tight junction strands of both AQP5+/+ and AQP5-/- male mice after pilocarpine stimulation but no change in strand number in female mice. Average acinar cell volume was increased by approximately 1.4-fold in glands from AQP5-/- mice, suggesting an alteration in the volume-sensing machinery of the cell. Western blots revealed that expression of Claudin-7, Claudin-3, and Occludin, critical proteins that regulate the permeability of the tight junction barrier, were significantly decreased in AQP5-/- compared with AQP5+/+ salivary glands. These findings reveal the existence of a gender-influenced molecular mechanism involving AQP5 that allows transcellular and paracellular routes of water transport to act in conjunction.
为了研究水运输的跨细胞途径和细胞旁途径之间潜在的生理相互作用,我们探究了唾液腺泡细胞中主要的跨细胞水通道蛋白5(AQP5)的靶向缺失是否会影响4 kDa异硫氰酸荧光素标记葡聚糖(FITC-D)的细胞旁运输,FITC-D通过细胞旁而非跨细胞途径运输。在向AQP5野生型或AQP5基因敲除小鼠静脉注射FITC-D并在固定时间间隔收集唾液后,我们发现,AQP5基因敲除小鼠唾液中运输的FITC-D相对量是匹配的AQP5野生型小鼠的一半,这表明缺乏AQP5的小鼠细胞旁屏障的通透性降低了2倍。我们还发现雄性和雌性小鼠在跨细胞运输与细胞旁运输的比例上存在显著差异。冷冻断裂电子显微镜显示,毛果芸香碱刺激后,AQP5野生型和AQP5基因敲除雄性小鼠的紧密连接链数量增加,但雌性小鼠的链数量没有变化。AQP5基因敲除小鼠腺体的腺泡细胞平均体积增加了约1.4倍,这表明细胞的体积传感机制发生了改变。蛋白质免疫印迹显示,与AQP5野生型唾液腺相比,AQP5基因敲除唾液腺中Claudin-7、Claudin-3和闭合蛋白(Occludin)(调节紧密连接屏障通透性的关键蛋白)的表达显著降低。这些发现揭示了一种涉及AQP5的性别影响分子机制的存在,该机制使水运输的跨细胞途径和细胞旁途径协同作用。