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

被引:104
作者
Zhou, XB [1 ]
Ruth, P [1 ]
Schlossmann, J [1 ]
Hofmann, F [1 ]
Korth, M [1 ]
机构
[1] TECH UNIV MUNICH, INST PHARMAKOL & TOXIKOL, D-80802 MUNICH, GERMANY
关键词
D O I
10.1074/jbc.271.33.19760
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:19760 / 19767
页数:8
相关论文
共 50 条
[21]   K+ CHANNELS IN THE BASOLATERAL MEMBRANE OF RAT CORTICAL COLLECTING DUCT [J].
HIRSCH, J ;
SCHLATTER, E .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1993, 424 (5-6) :470-477
[22]   K+ CHANNELS IN THE BASOLATERAL MEMBRANE OF RAT CORTICAL COLLECTING DUCT ARE REGULATED BY A CGMP-DEPENDENT PROTEIN-KINASE [J].
HIRSCH, J ;
SCHLATTER, E .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1995, 429 (03) :338-344
[23]   ANP RELAXES BOVINE TRACHEAL SMOOTH-MUSCLE AND INCREASES CGMP [J].
ISHII, K ;
MURAD, F .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (03) :C495-C500
[24]  
ITO Y, 1978, J PHARMACOL EXP THER, V207, P1022
[25]   ACTIONS OF NITROGLYCERINE ON THE MEMBRANE AND MECHANICAL-PROPERTIES OF SMOOTH MUSCLES OF THE CORONARY-ARTERY OF THE PIG [J].
ITO, Y ;
KITAMURA, K ;
KURIYAMA, H .
BRITISH JOURNAL OF PHARMACOLOGY, 1980, 70 (02) :197-204
[26]  
JONES TR, 1990, J PHARMACOL EXP THER, V255, P697
[27]  
KOLB HA, 1990, REV PHYSIOL BIOCH P, V115, P51
[28]   POTASSIUM CHANNELS IN AIRWAY SMOOTH-MUSCLE - A TALE OF 2 CHANNELS [J].
KOTLIKOFF, MI .
PHARMACOLOGY & THERAPEUTICS, 1993, 58 (01) :1-12
[29]   STIMULATORY AND INHIBITORY REGULATION OF CALCIUM-ACTIVATED POTASSIUM CHANNELS BY GUANINE NUCLEOTIDE-BINDING PROTEINS [J].
KUME, H ;
GRAZIANO, MP ;
KOTLIKOFF, MI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (22) :11051-11055
[30]   BETA-ADRENERGIC AGONISTS REGULATE K-CA CHANNELS IN AIRWAY SMOOTH-MUSCLE BY CAMP-DEPENDENT AND CAMP-INDEPENDENT MECHANISMS [J].
KUME, H ;
HALL, IP ;
WASHABAU, RJ ;
TAKAGI, K ;
KOTLIKOFF, MI .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (01) :371-379