K. Melliti et al., Regulators of G protein signaling attenuate the G protein-mediated inhibition of N-type Ca channels, J GEN PHYSL, 113(1), 1999, pp. 97-109
Regulators of G protein signaling (RGS) proteins bind to the alpha subunits
of certain heterotrimeric G proteins and greatly enhance their rate of GTP
hydrolysis, thereby determining the time course of interactions among G al
pha, G beta gamma, and their effecters. Voltage-gated N-type Ca channels me
diate neurosecretion, and these Ca channels are powerfully inhibited by G p
roteins. To determine whether RGS proteins could influence Ca channel funct
ion, we recorded the activity of N-type Ca channels coexpressed in human em
bryonic kidney (HEK293) cells with G protein-coupled muscarinic (m2) recept
ors and various RGS proteins. Coexpression of full-length RGS3T, RGS3, or R
GS8 significantly attenuated the magnitude of receptor-mediated Ca channel
inhibition. In control cells expressing alpha 1B, alpha 2, and beta 3 Ca ch
annel subunits and m2 receptors, carbachol (1 mu M) inhibited whole-cell cu
rrents by similar to 80% compared with only similar to 55% inhibition in ce
lls also expressing exogenous RGS protein. A similar effect was produced by
expression of the conserved core domain of RGS8. The attenuation of Ca cur
rent inhibition resulted primarily from a shift in the steady state dose-re
sponse relationship to higher agonist concentrations, with the EC50 for car
bachol inhibition being similar to 18 nM in control cells vs. similar to 15
0 nM in RGS-expressing cells. The kinetics of Ca channel inhibition were al
so modified by RGS. Thus, in cells expressing RGS3T, the decay of prepulse
facilitation was slower, and recovery of Ca channels from inhibition after
agonist removal was faster than in control cells. The effects of RGS protei
ns on Ca channel modulation can be explained by their ability to act as GTP
ase-accelerating proteins for some G alpha subunits. These results suggest
that RGS proteins may play important roles in shaping the magnitude and kin
etics of physiological events, such as neurosecretion, that involve G prote
in-modulated Ca channels.