Ruiz-Ederra Javier, Verkman A S
Department of Medicine , Cardiovascular Research Institute, University of California, San Francisco, California 94143-0521, USA.
Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3960-7. doi: 10.1167/iovs.06-0229.
To investigate the involvement of aquaporin (AQP)-1 in lens epithelial cell water permeability and maintenance of lens transparency in experimental models of cataract formation.
Comparative studies were performed on wild-type versus AQP1-null mice. Osmotic water permeability was measured in calcein-stained epithelial cells in intact lenses from fluorescence changes in response to osmotic gradients. Lens water content was measured by gravimetry using kerosene-bromobenzene density gradients, and from wet/dry weight measurements. Lens transparency was measured by contrast analysis of transmitted grid images. Cataract formation was induced in vitro by incubation in high-glucose solutions and in vivo by acetaminophen toxicity.
Immunofluorescence showed AQP1 expression in wild-type mice in epithelial cells covering the anterior surface of the lens. AQP1 deletion did not alter baseline lens morphology or transparency, though basal water content was approximately 3% greater (P < 0.001). AQP1 deficiency reduced plasma membrane water permeability in lens epithelium by 2.8 +/- 0.3-fold (P < 0.0001). Loss of lens transparency was accelerated by more than 50-fold in AQP1-null lenses bathed in a 55-mM glucose solution for 18 hours. At 4 hours after acetaminophen administration in 3-methylcholantrene-treated mice, lens opacification was seen in none of the six wild-type mice and in six of six AQP1-null mice.
Lens AQP1 facilitates the maintenance of transparency and opposes cataract formation.
在白内障形成的实验模型中,研究水通道蛋白(AQP)-1在晶状体上皮细胞水通透性及晶状体透明度维持中的作用。
对野生型小鼠和AQP1基因敲除小鼠进行比较研究。通过完整晶状体中钙黄绿素染色上皮细胞对渗透压梯度的荧光变化来测量渗透水通透性。使用煤油 - 溴苯密度梯度通过重量法以及通过湿/干重测量来测定晶状体含水量。通过对透射网格图像的对比度分析来测量晶状体透明度。在高糖溶液中孵育体外诱导白内障形成,通过对乙酰氨基酚毒性体内诱导白内障形成。
免疫荧光显示野生型小鼠晶状体前表面覆盖的上皮细胞中有AQP1表达。AQP1基因缺失虽未改变晶状体的基线形态或透明度,但基础含水量大约高3%(P < 0.001)。AQP1缺乏使晶状体上皮细胞质膜水通透性降低2.8±0.3倍(P < 0.0001)。在55 mM葡萄糖溶液中孵育18小时后,AQP1基因敲除的晶状体透明度丧失加速超过50倍。在3 - 甲基胆蒽处理的小鼠中给予对乙酰氨基酚4小时后,6只野生型小鼠均未出现晶状体混浊,而6只AQP1基因敲除小鼠中有6只出现晶状体混浊。
晶状体AQP1有助于维持透明度并对抗白内障形成。