Metabolic Oscillations in Pancreatic Beta-Cells

胰腺β细胞的代谢振荡

基本信息

批准号：
8220971
负责人：
Matthew J. Merrins
金额：
$ 5.39万
依托单位：
UNIVERSITY OF MICHIGAN AT ANN ARBOR
依托单位国家：
美国
项目类别：
财政年份：
2010
资助国家：
美国
起止时间：
2010-03-01 至 2013-02-28
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8220971
关键词：
6-Phosphofructokinase Accounting Action Potentials Address Affect Behavior Beta Cell Binding Biological Assay Biosensor Computer Simulation Coupling Defect Development Diagnosis Diazoxide Disease Electrophysiology (science)Engineering Enzymes Exhibits Feedback Fluorescence Resonance Energy Transfer Foundations Fructose Fructose-2,6-bisphosphatase Glucokinase Glucose Glycolysis Goals Image In Vitro Insulin Islets of Langerhans Kinetics Knowledge Lead Left Life Measurement Mediating Membrane Membrane Potentials Metabolic Metabolic Diseases Metabolism Modeling Monitor Mus Non-Insulin-Dependent Diabetes Mellitus Optics Patients Pattern Phase Phosphotransferases Physiologic pulse Physiology Plasma Production Property Reaction Regulation Relative (related person)Research Design Signal Transduction Small Interfering RNA Structure of beta Cell of islet Testing Transplantation base enzyme activity fructose-6-phosphate improved in vivo insight insulin secretion islet mathematical model mitochondrial membrane novel novel strategies patch clamp prevent research study sensor time use voltage clamp

项目摘要

DESCRIPTION (provided by applicant): Secretion of insulin from beta-cells of pancreatic islets is biphasic and pulsatile. Loss of first phase secretion and steady-state plasma insulin oscillations are an early development in Type 2 diabetes mellitus. Despite extensive study of the signaling cascades underlying glucose-stimulated insulin secretion, it remains unclear how oscillations in insulin secretion arise. Our overall hypothesis is that slow oscillations in islet metabolism and insulin secretion reflect slow oscillations in glycolyis. Based on this hypothesis, a computational model has been developed in which slow glycolytic oscillations mediated by phosphofructokinase-1 (PFK1) interact with fast oscillations arising from membrane electrical activity and Ca2+ (the 'Dual Oscillator Model', or DOM). Although the DOM can uniquely account for the diversity of oscillatory patterns observed in islets in vitro and in vivo, direct evidence for beta-cell glycolytic oscillations is lacking, leaving the open question of whether metabolic oscillations are intrinsic, as the DOM predicts, or driven by Ca2+ oscillations, as proposed in competing models. To test the predictions of the DOM at the level of metabolic activity, we propose to examine whether glucokinase and phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB), which are regulators of PFK1, represent oscillatory parameters that modulate metabolism-secretion coupling in islets. Dynamic FRET imaging using novel metabolic sensors will be combined with patch-clamp electrophysiology, mathematical modeling, and optical measurements of Ca2+ and NAD(P)H, to address the following Specific Aims: 1. Define the spatial and temporal properties of glucokinase activation, including regulation via its binding partner PFKFB, and assess their respective contributions to the modulation of metabolic oscillations. 2. Modify the Dual Oscillator Model to incorporate changes in glycolytic flux and islet oscillatory behavior induced by glucokinase/PFKFB interaction and fructose-2,6-bisphosphate production by PFKFB. 3. Determine whether Ca2+ drives changes in metabolism, metabolism drives Ca2+, or both occur.

描述（由申请人提供）：胰岛β细胞分泌的胰岛素是双相的和脉动的。第一相分泌丧失和稳态血浆胰岛素振荡是 2 型糖尿病的早期发展。尽管对葡萄糖刺激胰岛素分泌的信号级联进行了广泛的研究，但仍不清楚胰岛素分泌的振荡是如何产生的。我们的总体假设是，胰岛代谢和胰岛素分泌的缓慢振荡反映了糖酵解的缓慢振荡。基于这一假设，我们开发了一种计算模型，其中磷酸果糖激酶 1 (PFK1) 介导的缓慢糖酵解振荡与膜电活动和 Ca2+ 产生的快速振荡相互作用（“双振荡器模型”或 DOM）。尽管 DOM 可以独特地解释体外和体内胰岛中观察到的振荡模式的多样性，但缺乏 β 细胞糖酵解振荡的直接证据，留下了一个悬而未决的问题：代谢振荡是否如 DOM 预测的那样是内在的，还是驱动的正如竞争模型中所提出的那样，由 Ca2+ 振荡引起。为了测试代谢活性水平上 DOM 的预测，我们建议检查作为 PFK1 调节因子的葡萄糖激酶和磷酸果糖 2-激酶/果糖 2,6-二磷酸酶 (PFKFB) 是否代表调节代谢的振荡参数-胰岛中的分泌耦合。使用新型代谢传感器的动态 FRET 成像将与膜片钳电生理学、数学建模以及 Ca2+ 和 NAD(P)H 的光学测量相结合，以解决以下具体目标： 1. 定义葡萄糖激酶激活的空间和时间特性，包括通过其结合伙伴 PFKFB 进行调节，并评估它们各自对代谢振荡调节的贡献。 2.修改双振荡器模型，以纳入由葡萄糖激酶/PFKFB相互作用和PFKFB产生的2,6-二磷酸果糖引起的糖酵解通量和胰岛振荡行为的变化。 3. 确定是 Ca2+ 驱动新陈代谢变化，还是新陈代谢驱动 Ca2+，或两者同时发生。