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
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.