Thorn P, Gerasimenko O, Petersen O H
Physiological Laboratory, University of Liverpool, UK.
EMBO J. 1994 May 1;13(9):2038-43. doi: 10.1002/j.1460-2075.1994.tb06478.x.
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 (InsP3) 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 InsP3 receptor antagonist heparin. Our results indicate that both the ryanodine and the InsP3 receptors are involved in Ca2+ spike generation.
我们研究了对ryanodine敏感的细胞内Ca2+释放通道(ryanodine受体)在乙酰胆碱(ACh)或胆囊收缩素(CCK)诱发的胰腺腺泡细胞胞质Ca2+振荡中的作用。Ryanodine消除或显著抑制了激动剂诱发的Ca2+尖峰,但增加了通过直接向细胞内施加肌醇三磷酸(InsP3)所诱发的尖峰频率。我们还研究了环ADP-核糖(cADP-核糖)这种控制ryanodine受体的假定第二信使在Ca2+振荡中发挥作用的可能性。我们发现cADP-核糖自身可诱导位于分泌极的重复性Ca2+尖峰,并且这些尖峰被ryanodine阻断,但也被InsP3受体拮抗剂肝素阻断。我们的结果表明ryanodine受体和InsP3受体均参与Ca2+尖峰的产生。