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()
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
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.