Vectorial Ca2+ release via ryanodine receptors contributes to Ca2+ extrusion from freshly isolated rabbit aortic endothelial cells
CELL CALCIUM, vol.36, no.5, pp.431-443, 2004 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 36 Issue: 5
- Publication Date: 2004
- Doi Number: 10.1016/j.ceca.2004.04.003
- Journal Name: CELL CALCIUM
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.431-443
- Keywords: plasmalemmal Ca2+-ATPase, ryanodine receptors, Na+/Ca2+ exchanger, Ca2+ extrusion, endothelial cells, SKELETAL-MUSCLE, RETICULUM CA2+-ATPASE, CALCIUM, ACTIVATION, NAADP, STORE
- Ankara University Affiliated: No
Abstract
In this study, we identified ryanodine receptors (RyRs) as a component of a cytosolic Ca2+ removal pathway in freshly isolated rabbit aortic endothelial cells. In an earlier article, we reported that the sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) and Na+/Ca2+ exchanger (NCX) function in series to extrude cytosolic Ca2+ to the extracellular space. Here we employed caffeine and ryanodine as modulators of RyR and showed that they act as the linkage between SERCA and NCX in removing Ca2+ from the cytoplasm. Our data indicate that both 15 mM caffeine and 1 muM ryanodine facilitated Ca2+ extrusion by activating RyRs while 100 muM ryanodine had the opposite effect by blocking RyRs. A further attempt to investigate RyR pharmacology revealed that in the absence of extracellular Ca2+, ryanodine at 1 KM, but not 100 muM, stimulated Ca2+ loss from the endoplasmic reticulum (ER). Blockade of RyR had no effect on the Ca2+ removal rate when NCX had been previously blocked. In addition, the localization of RyR was determined using confocal microscopy of BODIPY TR-X fluorescent staining. Taken together, our findings suggest that in freshly isolated endothelial cells Ca2+ is removed in part by transport through SERCA, RyR, and eventually NCX, and that RyR and NCX are in close functional proximity near the plasma membrane. After blockade of this component, Ca2+ extrusion could be further inhibited by carboxyeosin, indicating a parallel contribution by the plasmalemmal Ca2+-ATPase (PMCA). (C) 2004 Elsevier Ltd. All rights reserved.