CaMK II and PKC inhibitors attenuated Ca2+-induced K+ channel inhibition in rat CCD cells to 83.2% and 50.7% of control values, respectively, with combined inhibition completely abolishing the effect.
Does CaMK II mediate Ca2+-induced K+ channel inhibition in rat CCD principal cells?
CaMK II, along with PKC, is involved in mediating the Ca2+-induced inhibition of the apical K+ channel in rat cortical collecting duct principal cells.
The apical low-conductance K+ channel of rat cortical collecting duct (CCD) is inhibited by increased intracellular Ca2+ concentrations. This effect has been shown to be mediated at least in part by activation of protein kinase C (PKC). In the present study, we used the patch-clamp technique to examine the role of Ca2+/calmodulin-dependent protein kinase II (CaMK II) in mediating the Ca(2+)-induced inhibitory effect. In cell-attached patches of principal cells of rat tubules, clamping of intracellular Ca2+ concentration at 400 nM by using 1 microM ionomycin reduced channel activity to 26.5% of the control value. A further reduction in channel activity, to 8.8% of the control value, was observed following the addition of phorbol 12-myristate 13-acetate (PMA), an agent known to activate PKC. Pretreatment of cells with KN-62 (CaMK II inhibitor) or GF-109203X (PKC inhibitor) attenuated the inhibitory effect of Ca2+ on K+ channel activity (83.2 and 50.7% of the control value, respectively). Even in the presence of KN-62, addition of 10 microM PMA significantly decreased channel activity to 57.2% of the control value. The Ca(2+)-induced inhibition was completely abolished by simultaneous incubation with both KN-62 and GF-109203X. In inside-out patches, addition of 20 micrograms/ml CaMK II in the presence of a PKC inhibitor reduced channel activity to 66.2% of control values. It is concluded that CaMK II is involved in mediating the Ca(2+)-induced inhibition of the activity of the apical K+ channel of rat CCD.
Kubokawa et al. (Wed,) reported a other. KN-62 (CaMK II inhibitor) and GF-109203X (PKC inhibitor) vs. Control (baseline channel activity) was evaluated on Apical low-conductance K+ channel activity. CaMK II and PKC inhibitors attenuated Ca2+-induced K+ channel inhibition in rat CCD cells to 83.2% and 50.7% of control values, respectively, with combined inhibition completely abolishing the effect.