PROTEIN PHOSPHATASE 2A IS ESSENTIAL FOR THE ACTIVATION OF CA2-ACTIVATED K+ CURRENTS BY CGMP-DEPENDENT PROTEIN-KINASE IN TRACHEAL SMOOTH-MUSCLE AND CHINESE-HAMSTER OVARY CELLS()

Citation
Xb. Zhou et al., PROTEIN PHOSPHATASE 2A IS ESSENTIAL FOR THE ACTIVATION OF CA2-ACTIVATED K+ CURRENTS BY CGMP-DEPENDENT PROTEIN-KINASE IN TRACHEAL SMOOTH-MUSCLE AND CHINESE-HAMSTER OVARY CELLS(), The Journal of biological chemistry, 271(33), 1996, pp. 19760-19767
Citations number
50
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
271
Issue
33
Year of publication
1996
Pages
19760 - 19767
Database
ISI
SICI code
0021-9258(1996)271:33<19760:PP2IEF>2.0.ZU;2-P
Abstract
The regulation of Ca2+ activated K+ channels (K-Ca channels) by cGMP-d ependent protein kinase (cGMP kinase) and its molecular mechanism were investigated in Chinese hamster ovary (CHO) and tracheal smooth muscl e 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 w ith intermediate conductance (similar to 50 picosiemens) were identifi ed, Due to the basal activity of cGMP kinase, Ca2+-activated K+ curren ts had a higher sensitivity toward the cytosolic Ca2+ concentration in CHO-cGK cells than in CHO-WT cells. Dialysis of the active fragment o f 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 s mooth muscle cells, the open state probability (NPo) of maxi-K-Ca chan nels (conductance of similar to 260 picosiemens) was enhanced by 300 m u M 8-(4-chlorophenylthio)-cGMP, a specific and potent activator of cG MP 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 in side-out patches, only the active fragment of cGMP kinase (but not tha t 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 in hibitor MT 5823 (1 mu M) and the protein phosphatase (PP) inhibitors m icrocystin (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 regu lates two different K-Ca channels in two unrelated cell types by the s ame indirect mechanism, which requires the activity of PP2A. The regul ation of the K-Ca channel is specific for cGMP kinase and is not mimic ked by cAMP kinase.