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Regulation of <i>I</i> <sub>Cl,swell</sub> in neuroblastoma cells by G protein signaling pathways
41
Citations
48
References
2001
Year
Cellular PharmacologyPertussis ToxinNeuroblastoma CellsCellular PhysiologySignaling PathwayCell RegulationCell InteractionMembrane TransportCell SignalingCholera ToxinG ProteinCell PhysiologyMolecular SignalingMolecular PhysiologyG Protein-coupled ReceptorPharmacologyCell BiologyDevelopmental BiologySignal TransductionSwelling-induced ActivationCellular BiochemistryMedicine
Guanosine 5'-O-(3-thiotriphosphate) (GTPgammaS) activated the I(Cl,swell) anion channel in N1E115 neuroblastoma cells in a swelling-independent manner. GTPgammaS-induced current was unaffected by ATP removal and broadly selective tyrosine kinase inhibitors, demonstrating that phosphorylation events do not regulate G protein-dependent channel activation. Pertussis toxin had no effect on GTPgammaS-induced current. However, cholera toxin inhibited the current approximately 70%. Exposure of cells to 8-bromoadenosine 3',5'-cyclic monophosphate did not mimic the effect of cholera toxin, and its inhibitory action was not prevented by treatment of cells with an inhibitor of adenylyl cyclase. These results demonstrate that GTPgammaS does not act through Galpha(i/o) GTPases and that Galpha(s)/Gbetagamma G proteins inhibit the channel and/or channel regulatory mechanisms through cAMP-independent mechanisms. Swelling-induced activation of I(Cl,swell) was stimulated two- to threefold by GTPgammaS and inhibited by 10 mM guanosine 5'-O-(2-thiodiphosphate). The Rho GTPase inhibitor Clostridium difficile toxin B inhibited both GTPgammaS- and swelling-induced activation of I(Cl,swell). Taken together, these findings indicate that Rho GTPase signaling pathways regulate the I(Cl,swell) channel via phosphorylation-independent mechanisms.
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