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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

Rapid desensitization of G protein-gated inwardly rectifying K⁺ currents is determined by G protein cycle

British Heart Foundation Laboratories and Department of Medicine, University College London, London WC1E 6JJ, United Kingdom

Submitted 2 December 2003 ; accepted in final form 8 March 2004

Activation of G protein-gated inwardly rectifying K⁺ (GIRK) channels, found in the brain, heart, and endocrine tissue, leads to membrane hyperpolarization that generates neuronal inhibitory postsynaptic potentials, slows the heart rate, and inhibits hormone release. During stimulation of G_i/o-coupled receptors and subsequent channel activation, it has been observed that the current desensitizes. In this study we examined mechanisms underlying fast desensitization of cloned heteromeric neuronal Kir3.1+3.2A and atrial Kir3.1+3.4 channels and also homomeric Kir3.0 currents in response to stimulation of several G_i/o G protein-coupled receptors (GPCRs) expressed in HEK-293 cells (adenosine A₁, adrenergic _2A, dopamine D_2S, M₄ muscarinic, and GABA_B1b/2 receptors). We found that all agonist-induced currents displayed a similar degree of desensitization except the adenosine A₁ receptor, which exhibits an additional desensitizing component. Using the nonhydrolyzable GTP analog guanosine 5'-O-(3-thiotriphosphate) (GTPS), we found that this is due to a receptor-dependent, G protein-independent process. Using Ca²⁺ imaging we showed that desensitization is unlikely to be accounted for solely by phospholipase C activation and phosphatidylinositol 4,5-bisphosphate (PIP₂) hydrolysis. We examined the contribution of the G protein cycle and found the following. First, agonist concentration is strongly correlated with degree of desensitization. Second, competitive inhibition of GDP/GTP exchange by using nonhydrolyzable guanosine 5'-O-(2-thiodiphosphate) (GDPS) has two effects, a slowing of channel activation and an attenuation of the fast desensitization phenomenon. Finally, using specific G subunits we showed that ternary complexes with fast activation rates display more prominent desensitization than those with slower activation kinetics. Together our data suggest that fast desensitization of GIRK currents is accounted for by the fundamental properties of the G protein cycle.

G protein-coupled receptor; potassium channel; inward rectifier; kinetics

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