Barth K, Weinhold K, Guenther A, Young M T, Schnittler H, Kasper M
Institute of Anatomy, Medical Faculty Carl Gustav Carus, Dresden University of Technology, Germany.
FEBS J. 2007 Jun;274(12):3021-33. doi: 10.1111/j.1742-4658.2007.05830.x. Epub 2007 May 11.
The P2X7 receptor has recently been described as a marker for lung alveolar epithelial type I cells. Here, we demonstrate both the expression of P2X7 protein and its partition into lipid rafts in the mouse lung alveolar epithelial cell line E10. A significant degree of colocalization was observed between P2X7 and the raft marker protein Caveolin-1; also, P2X7 protein was associated with caveolae. A marked reduction in P2X7 immunoreactivity was observed in lung sections prepared from Caveolin-1-knockout mice, indicating that Caveolin-1 expression was required for full expression of P2X7 protein. Indeed, suppression of Caveolin-1 protein expression in E10 cells using short hairpin RNAs resulted in a large reduction in P2X7 protein expression. Our data demonstrate a potential interaction between P2X7 protein and Caveolin-1 in lipid rafts, and provide a basis for further functional and biochemical studies to probe the physiologic significance of this interaction.
P2X7受体最近被描述为肺I型肺泡上皮细胞的标志物。在此,我们证明了P2X7蛋白在小鼠肺肺泡上皮细胞系E10中的表达及其在脂筏中的分布。观察到P2X7与脂筏标记蛋白小窝蛋白-1之间存在显著程度的共定位;此外,P2X7蛋白与小窝相关。在从小窝蛋白-1基因敲除小鼠制备的肺切片中观察到P2X7免疫反应性显著降低,表明小窝蛋白-1的表达是P2X7蛋白充分表达所必需的。事实上,使用短发夹RNA抑制E10细胞中小窝蛋白-1蛋白的表达导致P2X7蛋白表达大幅降低。我们的数据证明了P2X7蛋白与脂筏中的小窝蛋白-1之间存在潜在相互作用,并为进一步的功能和生化研究提供了基础,以探究这种相互作用的生理意义。