Temporal and quantitative correlations between insulin secretion and stably elevated or oscillatory cytoplasmic Ca2+ in mouse pancreatic β-cells

An increase in cytoplasmic Ca2+ in beta-cells is a key step in glucose-induced insulin secretion. However, whether changes in cytoplasmic free Ca2+ ([Ca2+](i)) directly regulate secretion remains disputed. This question was addressed by investigating the temporal and quantitative relationships between [Ca2+](i) and insulin secretion. Both events were measured simultaneously in single mouse islets loaded with fura-PE3 and perifused with a medium containing diazoxide (to prevent any effect of glucose on the membrane potential) and either 4.8 or 30 mmol/l K+. Continuous depolarization with 30 mmol/l K+ in the presence of 15 mmol/l glucose induced a sustained rise in [Ca2+], and insulin release. No oscillations of secretion were detected even after mathematical analysis of the data (pulse, spectral and sample distribution analysis). In contrast, alternating between 30 and 4.8 mmol/l K+ (1 min/2 min or 2.5 min/5 min) triggered synchronous [Ca-2'](i) and insulin oscillations of regular amplitude in each islet. A good correlation was found between [Ca2']i and insulin secretion, and it was independent of the presence or absence of oscillations. This quantitative correlation between [Ca2+](i) and insulin secretion was confirmed by experiments in which extracellular Ca2+ was increased or decreased (0.1-2.5 mmol/l) stepwise in the presence of 30 mmol/l KC. This resulted in parallel stepwise increases or decreases in [Ca2+](i) and insulin secretion. However, while the successive [Ca2+](i) levels were unaffected by glucose, each plateau of secretion was much higher in 20 than in 3 mmol/l glucose. In conclusion, in our preparation of normal mouse islets, insulin secretion oscillates only when [Ca2+](i), oscillates in beta-cells. This close temporal relationship between insulin secretion and [Ca2+](i) changes attests of the regulatory role of Ca2+ There also exists a quantitative relationship that is markedly influenced by the concentration of glucose.