M. Teubl et al., Na+/Ca2+ exchange facilitates Ca2+-dependent activation of endothelial nitric-oxide synthase, J BIOL CHEM, 274(41), 1999, pp. 29529-29535
Recent evidence suggests the expression of a Na+/ Ca2+ exchanger (NCX) in v
ascular endothelial cells, To elucidate the functional role of endothelial
NCX, we studied Ca2+ signaling and Ca2+-dependent activation of endothelial
nitric-oxide synthase (eNOS) at normal, physiological Na+ gradients and af
ter loading of endothelial cells with Na+ ions using the ionophore monensin
. Monensin-induced Na+ loading markedly reduced Ca2+ entry and, thus, stead
y-state levels of intracellular free Ca2+ ([Ca2+](i)) in thapsigargin-stimu
lated endothelial cells due to membrane depolarization. Despite this reduct
ion of overall [Ca2+](i), Ca2+-dependent activation of eNOS was facilitated
as indicated by a pronounced leftward shift of the Ca2+ concentration resp
onse curve in monensin-treated cells. This facilitation of Ca2+-dependent a
ctivation of eNOS was strictly dependent on the presence of Na+ ions during
treatment of the cells with monensin, Na+-induced facilitation of eNOS act
ivation was not due to a direct effect of Na+ ions on the Ca2+ sensitivity
of the enzyme. Moreover, the effect of Na+ was not related to Na+ entry-ind
uced membrane depolarization or suppression of Ca2+ entry, since neither el
evation of extracellular K+ nor the Ca2+ entry blocker 1-(beta-[3-(4-methox
yphenyl)-propoxy]-4-methoxyphenethyl)-1H-imidazole hydrochloride (SK&F 9636
5) mimicked the effects of Na+ loading. The effects of monensin were comple
tely blocked by 3',4'-dichlorobenzamil, a potent and selective inhibitor of
NCX, whereas the structural analog amiloride, which barely affects Na+/Ca2
+ exchange, was ineffective. Consistent with a pivotal role of Na+/Ca2+ exc
hange in Ca2+-dependent activation of eNOS, an NCX protein was detected in
caveolin-rich membrane fractions containing both eNOS and caveolin-1. These
results demonstrate for the first time a crucial role of cellular Na+ grad
ients in regulation of eNOS activity and suggest that a tight functional in
teraction between endothelial NCX and eNOS may take place in caveolae.