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.
机构:
Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
Pike, LJ
;
Miller, JM
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
机构:
Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
Pike, LJ
;
Miller, JM
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA