Thorn P, Lawrie A M, Smith P M, Gallacher D V, Petersen O H
Physiological Laboratory University of Liverpool, England.
Cell. 1993 Aug 27;74(4):661-8. doi: 10.1016/0092-8674(93)90513-p.
Submaximal stimulation with agonists generating inositol 1,4,5-trisphosphate (IP3) evokes cytosolic Ca2+ oscillations in many different cell types. In general, each Ca2+ rise is initiated from a specific region near the plasma membrane and then spreads as a wave throughout the cell. We now demonstrate that low (physiological) agonist concentrations evoke local cytosolic Ca2+ spikes in the secretory pole of single mouse pancreatic acinar cells that are particularly sensitive to blockade by the IP3 receptor antagonist heparin. These spikes can occur alone or repetitively or can precede longer lasting Ca2+ signals that spread throughout the cell. Intracellular IP3 application mimics these agonist actions. The short-lasting local Ca2+ spikes provide an economical signaling mechanism and are of physiological significance since they activate Ca(2+)-dependent Cl- and cation currents important for control of fluid secretion.
用能生成肌醇1,4,5-三磷酸(IP3)的激动剂进行次最大刺激,可在许多不同细胞类型中引发胞质Ca2+振荡。一般来说,每次Ca2+升高都从质膜附近的特定区域开始,然后作为一个波在整个细胞中传播。我们现在证明,低(生理)激动剂浓度可在单个小鼠胰腺腺泡细胞的分泌极引发局部胞质Ca2+尖峰,这些尖峰对IP3受体拮抗剂肝素的阻断特别敏感。这些尖峰可以单独出现或重复出现,也可以先于在整个细胞中传播的持续时间更长的Ca2+信号出现。细胞内应用IP3可模拟这些激动剂的作用。短暂的局部Ca2+尖峰提供了一种经济的信号传导机制,并且具有生理意义,因为它们可激活对控制液体分泌很重要的Ca(2+)依赖性Cl-和阳离子电流。