Gylfe E, Grapengiesser E, Liu Y J, Dryselius S, Tengholm A, Eberhardson M
Diabetes Metab. 1998 Feb;24(1):25-9.
Individual pancreatic beta cells respond to glucose stimulation with large amplitude (300-500 nM) oscillations in the cytoplasmic Ca2+ concentration ([Ca2+]i). These oscillations (frequency 0.05-0.5/min) depend on rhythmical depolarization of the plasma membrane, with influx of Ca2+ through voltage-operated channels, but do not require intracellular mobilization of Ca2+. Patch clamp analyses of the activity of ATP-sensitive K+ channels indicate that oscillations in beta-cell metabolism underlie the rhythmical depolarizations, causing the large amplitude oscillations of [Ca2+]. The oscillatory responses of adjacent beta cells are synchronized by gap-junctional coupling in cellular microdomains. With increasing glucose concentration, previously unresponsive domains are activated, and their oscillations entrained with those of other active domains. In pancreatic islets, glucose-induced large amplitude oscillations occur in parallel with insulin release pulses, the amplitudes of which are determined by the number of beta cells recruited into the secretory state.
单个胰腺β细胞对葡萄糖刺激的反应是细胞质Ca2+浓度([Ca2+]i)出现大幅度(300 - 500 nM)振荡。这些振荡(频率为0.05 - 0.5次/分钟)依赖于质膜的节律性去极化,Ca2+通过电压门控通道内流,但不需要细胞内Ca2+的动员。对ATP敏感性K+通道活性的膜片钳分析表明,β细胞代谢的振荡是节律性去极化的基础,导致了[Ca2+]的大幅度振荡。相邻β细胞的振荡反应通过细胞微区内的缝隙连接耦合实现同步。随着葡萄糖浓度的增加,先前无反应的区域被激活,其振荡与其他活跃区域的振荡同步。在胰岛中,葡萄糖诱导的大幅度振荡与胰岛素释放脉冲同时发生,胰岛素释放脉冲的幅度由进入分泌状态的β细胞数量决定。