首页> 美国卫生研究院文献>The EMBO Journal >Cyclic ADP-ribose regulation of ryanodine receptors involved in agonist evoked cytosolic Ca2+ oscillations in pancreatic acinar cells.
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Cyclic ADP-ribose regulation of ryanodine receptors involved in agonist evoked cytosolic Ca2+ oscillations in pancreatic acinar cells.

机译:参与激动剂的ryanodine受体的循环ADP核糖调节引起胰腺腺泡细胞中的胞质Ca2 +振荡。

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摘要

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.
机译:我们已经研究了由乙酰胆碱(ACh)或胆囊收缩素(CCK)引起的胰腺腺泡细胞中的胞质Ca2 +振荡中,雷诺丁碱敏感性细胞内Ca2 +释放通道(ryanodine受体)的作用。 Ryanodine消除或明显抑制了激动剂引起的Ca2 +突增,但增加了直接应用内部三磷酸肌醇(InsP3)引起的尖峰的频率。我们还研究了环状的ADP-核糖(cADP-核糖)(假定的第二信使控制了ryanodine受体)在Ca2 +振荡中起作用的可能性。我们发现,cADP-核糖本身可以诱导位于分泌极的重复Ca2 +峰,这些峰被ryanodine阻断,但也被InsP3受体拮抗剂肝素阻断。我们的结果表明,ryanodine和InsP3受体均参与Ca2 +尖峰的产生。

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