The regulation of Ca2+ activated K+ channels (K-Ca channels) by cGMP-dependent protein kinase (cGMP kinase) and its molecular mechanism were investigated in Chinese hamster ovary (CHO) and tracheal smooth muscle cells, In CHO wild-type cells (CHO-WT cells) and in CHO cells stably transfected with cGMP kinase I alpha (CHO-cGK cells), K-Ca channels with intermediate conductance (similar to 50 picosiemens) were identified, Due to the basal activity of cGMP kinase, Ca2+-activated K+ currents had a higher sensitivity toward the cytosolic Ca2+ concentration in CHO-cGK cells than in CHO-WT cells. Dialysis of the active fragment of cGMP kinase (300 nM) into CHO-WT cells or of cGMP into CHO-cGK cells increased the Ca2+-activated K+ current, while the catalytic subunit of cAMP-dependent protein kinase (cAMP kinase) was without effect, In cell-attached patches obtained from freshly isolated bovine tracheal smooth muscle cells, the open state probability (NPo) of maxi-K-Ca channels (conductance of similar to 260 picosiemens) was enhanced by 300 mu M 8-(4-chlorophenylthio)-cGMP, a specific and potent activator of cGMP kinase. In contrast, 1 mu M isoprenaline, 20 mu M forskolin, and 3 mM 8-bromo-cAMP failed to enhance K-Ca channel activity. In excised inside-out patches, only the active fragment of cGMP kinase (but not that of cAMP kinase) increased NPo when applied to the cytosolic side of the patch. The enhancement of NPo by cGMP kinase was inhibited in CHO cells as well as in tracheal smooth muscle cells by the cGMP kinase inhibitor MT 5823 (1 mu M) and the protein phosphatase (PP) inhibitors microcystin (5 mu M) and okadaic acid (10 nM). The catalytic subunit of PP2A (but not that of PP1) mimicked the effect of cGMP kinase on NPo in excised, inside-out patches. The results show that cGMP kinase regulates two different K-Ca channels in two unrelated cell types by the same indirect mechanism, which requires the activity of PP2A. The regulation of the K-Ca channel is specific for cGMP kinase and is not mimicked by cAMP kinase.