PROTEIN-KINASE INHIBITORS REDUCE SR CA TRANSPORT IN PERMEABILIZED CARDIAC MYOCYTES

Citation
A. Mattiazzi et al., PROTEIN-KINASE INHIBITORS REDUCE SR CA TRANSPORT IN PERMEABILIZED CARDIAC MYOCYTES, The American journal of physiology, 267(2), 1994, pp. 80000812-80000820
Citations number
46
Categorie Soggetti
Physiology
ISSN journal
00029513
Volume
267
Issue
2
Year of publication
1994
Part
2
Pages
80000812 - 80000820
Database
ISI
SICI code
0002-9513(1994)267:2<80000812:PIRSCT>2.0.ZU;2-A
Abstract
Phosphorylation of the sarcoplasmic reticulum (SR) protein phospholamb an by adenosine 3',5'-cyclic monophosphate (cAMP)-dependent protein ki nase (PKA) and Ca-calmodulin-dependent protein kinase (CaM-KII) stimul ates Ca-adenosinetriphosphatase (ATPase) activity and SR Ca transport, but the role of CaM-KII-dependent phosphorylation is not well defined . We studied the PKA- and CaM-KII-dependent regulation of SR Ca transp ort in digitonin-permeabilized rabbit ventricular myocytes. SR Ca upta ke and free Ca concentration were measured on line with indo 1 and Ca electrodes in the presence of 20 mu M ruthenium red and 10 mM oxalate. Neither N-6,2'-O-dibutyryl-cAMP (up to 500 mu M) nor the nonhydrolyza ble cAMP agonist adenosine 3'5'-cyclic monophosphorothioate sodium sal t (Sp-cAMP[S]; up to 275 mu M) affected the maximum uptake rate (V-max ) or the dissociation constant (K-d) for Ca uptake. However, the PKA i nhibitor H-89 significantly increased K-d (e.g., from 307 +/- 67 to 82 6 +/- 62 nM Ca at 40-65 mu M H-89) without significantly affecting V-m ax. Both CaM-KII inhibitors, KN-62 (60 mu M) and a CaM-KII inhibitory peptide (10 mu M), significantly decreased V-max from 11.95 +/- 0.5 to 9.48 +/- 0.6 nmol.mg(-1).min(-1) and from 10.95 +/- 1.72 to 7.37 +/- 0.94 nmol.mg(-1).min(-1), respectively, without consistently changing K-d The effects of H-89 on K-d and of KN-62 on V-max were prevented by a monoclonal antibody to phospholamban 2D12 (consistent with the anti body removing the inhibitory effect of phospholamban on the SR Ca-ATPa se). Clear effects of protein kinase inhibitors and lack of stimulator y effects lead us to conclude that the Ca pump may be close to maximal activation in our system (such that only inhibitory effects are appar ent). The results suggest that phospholamban phosphorylation by PKA an d CaM-KII, respectively, may produce functionally distinct effects on Ca transport by the SR. That is, phosphorylation of phospholamban by e ndogenous CaM-KII appears to increase the V-max of the SR Ca-ATPase, w hereas PKA increases the Ca affinity of the pump.