CYCLIC ADP-RIBOSE REGULATION OF RYANODINE RECEPTORS INVOLVED IN AGONIST-EVOKED CYTOSOLIC CA2+ OSCILLATIONS IN PANCREATIC ACINAR-CELLS
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THORN, P
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UNIV LIVERPOOL, PHYSIOL LAB, MRC, SECRETORY CONTROL RES GRP, LIVERPOOL L69 3BX, ENGLANDUNIV LIVERPOOL, PHYSIOL LAB, MRC, SECRETORY CONTROL RES GRP, LIVERPOOL L69 3BX, ENGLAND
THORN, P
[1
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GERASIMENKO, O
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UNIV LIVERPOOL, PHYSIOL LAB, MRC, SECRETORY CONTROL RES GRP, LIVERPOOL L69 3BX, ENGLANDUNIV LIVERPOOL, PHYSIOL LAB, MRC, SECRETORY CONTROL RES GRP, LIVERPOOL L69 3BX, ENGLAND
GERASIMENKO, O
[1
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PETERSEN, OH
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UNIV LIVERPOOL, PHYSIOL LAB, MRC, SECRETORY CONTROL RES GRP, LIVERPOOL L69 3BX, ENGLANDUNIV LIVERPOOL, PHYSIOL LAB, MRC, SECRETORY CONTROL RES GRP, LIVERPOOL L69 3BX, ENGLAND
PETERSEN, OH
[1
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[1] UNIV LIVERPOOL, PHYSIOL LAB, MRC, SECRETORY CONTROL RES GRP, LIVERPOOL L69 3BX, ENGLAND
We have investigated the role of the ryanodine-sensitive intracellular Ca2+ release channel (ryanodine receptor) in the cytosolic Ca2+ oscillations evoked in pancreatic acinar cells by acetylcholine (ACh) or cholecystokinin (CCK). Ryanodine abolished or markedly inhibited the agonist evoked Ca2+ spiking, but enhanced the frequency of spikes evoked by direct internal inositol trisphosphate (InsP(3)) application. We have also investigated the possibility that cyclic ADP-ribose (cADP-ribose), the putative second messenger controlling the ryanodine receptor, plays a role in Ca2+ oscillations. We found that cADP-ribose could itself induce repetitive Ca2+ spikes localized in the secretory pole and that these spikes were blocked by ryanodine, but also by the InsP(3) receptor antagonist heparin. Our results indicate that both the ryanodine and the InsP(3) receptors are involved in Ca2+ spike generation.