Cl- current activation in choroid plexus epithelial cells involves a G protein and protein kinase A

The involvement of GTP-binding proteins (G proteins) in the regulation of the Cl- conductance in rat choroid plexus epithelial cells was investigated, using the whole cell patch-clamp technique. Intracellular application of a nonhydrolyzable GTP analogue, guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S; 0.1-0.2 mM), evoked a transient increase in the Cl- conductance. The activated Cl- current exhibited inward rectification and was independent of time at hyperpolarizing or depolarizing voltage pulses. The effect of GTP gamma S was inhibited by a nonhydrolyzable GDP analogue, guanosine 5'-O-(2-thiodiphosphate) (2 mM), and by an inhibitor of protein kinase A, H-89, but was not affected by chelation of cytosolic Ca2+ with 5 mM 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid. GTP gamma S failed to activate the current when ATP was omitted from the pipette solution. Intracellular application of adenosine 3',5'-cyclic monophosphate (cAMP; 0.25 mM) or the catalytic subunit of protein kinase A activated a similar Cl- current. These results suggest that G proteins activate Cl- channels via a cAMP-dependent pathway in rat choroid plexus.