Interaction and interrelation of P2X7 and P2X4 receptor complexes in mouse lung epithelial cells

被引:49
作者
Weinhold, Karina [1 ]
Krause-Buchholz, Udo [2 ]
Roedel, Gerhard [2 ]
Kasper, Michael [1 ]
Barth, Kathrin [1 ]
机构
[1] Tech Univ Dresden, Fac Med, Inst Anat, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Inst Genet, Fac Sci, D-01307 Dresden, Germany
关键词
P2X protein complexes; Caveolin-1; Caveolae; Epithelial lung cells; Native PAGE; LIPID RAFTS; PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; FUNCTIONAL EVIDENCE; CHANNEL ENAC; ION CHANNELS; SUBUNITS; P2X(4); CARDIOLIPIN; EXPRESSION; CAVEOLAE;
D O I
10.1007/s00018-010-0355-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P2X4 and P2X7 receptors are ATP-gated ion channels that are co-expressed in alveolar epithelial type I cells. Both receptors are localized to the plasma membrane and partly associated with lipid rafts. Here we report on our study in an alveolar epithelial cell line of the molecular organization of P2X7R and P2X4R receptors and the effect of their knockdown. Native gel electrophoresis reveals three P2X7R complexes of similar to 430, similar to 580 and similar to 760 kDa. The latter two correspond exactly in size to signals of Cav-1, the structural protein of caveolae. Interestingly knockdown of P2rx7 affects protein levels, the intracellular distribution and the supramolecular organization of Cav-1 as well as of P2X4R, which is mainly detected in a complex of similar to 430 kDa. Our data suggest upregulation of P2X4R as a compensatory mechanism of P2X7R depletion.
引用
收藏
页码:2631 / 2642
页数:12
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