Constitutive activity of inwardly rectifying K⁺ channel at physiological [Ca]_i is mediated by Ca²⁺/CaMK II pathway in opossum kidney proximal tubule cells

Using patch-clamp technique, we studied the role of the Ca ²⁺/calmodulin kinase II (CaMK II)-mediated phosphorylation process on the K⁺ channel with an inward conductance of 90 pS in opossum kidney proximal tubule cells (OKPCs). The intracellular Ca²⁺ concentration ([Ca]_i) was measured by use of the fluorescent dye fura 2. The following results were obtained: (i) In cell-attached patches, the channel activity was inhibited by a decrease in [Ca]_i induced by perfusion with low Ca²⁺ (10^-8 M), La³⁺ (100 μM), or EGTA/AM (100 μM) contained in the bath solution. The application of KN-62 (10 μM) or KN-93 (5 μM), inhibitors of CaMK II, also inhibited the channel activity. (ii) The membrane potential measured with nystatin-perforated patches was significantly decreased by the fall in [Ca]_i induced by the perfusion with EGTA- or La³⁺-containing solution. Also, the application of KN-62 (10 μM) or KN-93 (5 μM) to the bath significantly decreased the membrane potential. (iii) In inside-out patches, the channel activity was significantly stimulated by the application of CaMK II (300 pM) at 10^-7 M Ca²⁺ in the bath. Furthermore, the application of KN-62 (10 μM) to the bath significantly decreased the channel activity. Our findings show that the constitutive activity of inwardly rectifying K ⁺ channel at physiological [Ca]_i is mediated by the Ca²⁺/CaMK II pathway in OKPCs.