Berts A, Gylfe E, Hellman B
Department of Medical Cell Biology, Uppsala University, Sweden.
Biochem Biophys Res Commun. 1995 Mar 17;208(2):644-9. doi: 10.1006/bbrc.1995.1387.
Immunohistochemically identified glucagon-releasing alpha 2-cells from mouse pancreatic islets exhibited large amplitude oscillations of the cytoplasmic Ca2+ concentration in 3 mM glucose. Other small islet cells with similar oscillations in the presence of 20 mM glucose were identified as somatostatin-releasing alpha 1-cells. The oscillations in both cell types resembled those induced by glucose in the surrounding larger beta-cells in starting from the basal level and disappearing after addition of the voltage-dependent Ca2+ channel blocker methoxyverapamil. The discovery that the alpha 1- and alpha 2-cells have intrinsic abilities to generate oscillatory Ca2+ signals indicates that pulsatile release of somatostatin and glucagon do not require functional coupling to the beta-cells.
免疫组化鉴定出的来自小鼠胰岛的胰高血糖素释放α2细胞,在3 mM葡萄糖条件下表现出细胞质Ca2+浓度的大幅度振荡。在20 mM葡萄糖存在下具有类似振荡的其他小胰岛细胞被鉴定为生长抑素释放α1细胞。两种细胞类型中的振荡,从基础水平开始,在添加电压依赖性Ca2+通道阻滞剂甲氧基维拉帕米后消失,这与周围较大的β细胞中葡萄糖诱导的振荡相似。α1和α2细胞具有产生振荡性Ca2+信号的内在能力这一发现表明,生长抑素和胰高血糖素的脉冲式释放不需要与β细胞进行功能耦合。