Kamagate Adama, Herchuelz André, Van Eylen Françoise
Laboratory of Pharmacology, Brussels University School of Medicine, Brussels, Belgium.
Diabetes. 2002 Sep;51(9):2773-88. doi: 10.2337/diabetes.51.9.2773.
In the mouse beta-cell, glucose generates large amplitude oscillations of the cytosolic-free Ca(2+) concentration (Ca(2+)) that are synchronous to insulin release oscillations. To examine the role played by Ca(2+) oscillations in the process of insulin release, we examined the effect of plasma membrane Ca(2+)-ATPase (PMCA) overexpression on glucose-induced Ca(2+) oscillations and insulin release in BRIN-BD11 cells. BRIN-BD11 cells were stably transfected with PMCA2wb. Overexpression could be assessed at the mRNA and protein level, with appropriate targeting to the plasma membrane assessed by immunofluorescence and the increase in PMCA activity. In response to K(+), overexpressing cells showed a markedly reduced rise in Ca(2+). In response to glucose, control cells showed large amplitude Ca(2+) oscillations, whereas overexpressing cells showed markedly reduced increases in Ca(2+) without such large oscillations. Suppression of Ca(2+) oscillations was accompanied by an increase in glucose metabolism and insulin release that remained oscillatory despite having a lower periodicity. Hence, [Ca(2+)] (i) oscillations appear unnecessary for glucose-induced insulin release and may even be less favorable than a stable increase in Ca(2+) for optimal hormone secretion. Ca(2+) oscillations do not directly drive insulin release oscillations but may nevertheless intervene in the fine regulation of such oscillations.
在小鼠β细胞中,葡萄糖可引起胞质游离Ca(2+)浓度(Ca(2+))的大幅度振荡,该振荡与胰岛素释放振荡同步。为了研究Ca(2+)振荡在胰岛素释放过程中所起的作用,我们检测了质膜Ca(2+)-ATP酶(PMCA)过表达对BRIN-BD11细胞中葡萄糖诱导的Ca(2+)振荡和胰岛素释放的影响。BRIN-BD11细胞用PMCA2wb进行稳定转染。过表达可在mRNA和蛋白质水平进行评估,通过免疫荧光评估其对质膜的适当靶向作用以及PMCA活性的增加。对K(+)的反应中,过表达细胞的Ca(2+)升高明显降低。对葡萄糖的反应中,对照细胞显示出大幅度的Ca(2+)振荡,而过表达细胞的Ca(2+)升高明显降低,且无此类大幅度振荡。Ca(2+)振荡的抑制伴随着葡萄糖代谢和胰岛素释放的增加,尽管其周期性较低,但仍保持振荡。因此,Ca(2+)振荡对于葡萄糖诱导的胰岛素释放似乎并非必要,甚至对于最佳激素分泌而言,可能比Ca(2+)的稳定升高更不利。Ca(2+)振荡并不直接驱动胰岛素释放振荡,但仍可能参与此类振荡的精细调节。