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Complex Patterns of Metabolic and Ca2+ Entrainment in Pancreatic Islets by Oscillatory Glucose

机译:振荡葡萄糖在胰岛中代谢和Ca 2+夹带的复杂模式

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摘要

Glucose-stimulated insulin secretion is pulsatile and driven by intrinsic oscillations in metabolism, electrical activity, and Ca2+ in pancreatic islets. Periodic variations in glucose can entrain islet Ca2+ and insulin secretion, possibly promoting interislet synchronization. Here, we used fluorescence microscopy to demonstrate that glucose oscillations can induce distinct 1:1 and 1:2 entrainment of oscillations (one and two oscillations for each period of exogenous stimulus, respectively) in islet Ca2+, NAD(P)H, and mitochondrial membrane potential. To our knowledge, this is the first demonstration of metabolic entrainment in islets, and we found that entrainment of metabolic oscillations requires voltage-gated Ca2+ influx. We identified diverse patterns of 1:2 entrainment and showed that islet synchronization during entrainment involves adjustments of both oscillatory phase and period. All experimental findings could be recapitulated by our recently developed mathematical model, and simulations suggested that interislet variability in 1:2 entrainment patterns reflects differences in their glucose sensitivity. Finally, our simulations and recordings showed that a heterogeneous group of islets synchronized during 1:2 entrainment, resulting in a clear oscillatory response from the collective. In summary, we demonstrate that oscillatory glucose can induce complex modes of entrainment of metabolically driven oscillations in islets, and provide additional support for the notion that entrainment promotes interislet synchrony in the pancreas.
机译:葡萄糖刺激的胰岛素分泌是脉动的,并受胰岛中新陈代谢,电活动和Ca 2 + 的固有振荡的驱动。葡萄糖的周期性变化会夹带胰岛Ca 2 + 和胰岛素分泌,可能促进胰岛间同步。在这里,我们使用荧光显微镜来证明葡萄糖振荡可以诱导胰岛Ca 2 + 中不同的1:1和1:2振荡夹带(每个外源刺激周期分别为一个和两个振荡)。 ,NAD(P)H和线粒体膜电位。据我们所知,这是胰岛中新陈代谢夹带的首次证明,我们发现新陈代谢夹带需要电压门控的Ca 2 + 涌入。我们确定了1:2夹带的多种模式,并表明夹带期间的胰岛同步涉及振荡相位和周期的调整。我们最近开发的数学模型可以概括所有实验结果,并且模拟表明,1:2夹带模式的小岛间变异反映了其葡萄糖敏感性的差异。最后,我们的模拟和记录表明,一组异质的胰岛在1:2的夹带过程中同步,从而导致来自集合体的清晰振荡响应。总之,我们证明振荡葡萄糖可以诱导胰岛中新陈代谢驱动的振荡的复杂模式的夹带,并为夹带促进胰岛间同步的观点提供了额外的支持。

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