Dopamine Action in Pancreatic Islet Function

多巴胺在胰岛功能中的作用

• 批准号: 9068606
• 负责人: David W Piston
• 金额: $ 12.75万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-07-23 至 2016-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9068606
• 关键词: Dopamine; Action; Pancreatic; Islet; Function

DESCRIPTION (provided by applicant): Project Summary The long term goal of this research is to determine the mechanism and effect of dopamine signaling on hormone secretion from the islet of Langerhans. Blood glucose homeostasis depends on glucose-stimulated insulin secretion (GSIS) from islet 2 cells, but we also know that non-glucose signals are important for modulating insulin secretion, and many of these signals are known to communicate through G-protein coupled receptors. Dopamine acts through a number of G-protein coupled receptors, but its signaling in the 2-cell has not been well-characterized. All current antipsychotic drugs block D2 dopamine receptors as well as other targets, and the most effective second generation antipsychotics cause significant metabolic side-effects leading to increased risks of obesity and diabetes. Unfortunately, there is no consensus about the molecular mechanisms underlying the side-effects. Since all of these anti-psychotics block D2 receptors, but not all have notable metabolic side-effects, it has been assumed that the side-effects are mediated by interactions with molecules other than D2 receptors. The 2-cell has drawn little attention as a potential target of these drugs, presumably because there are no known dopaminergic neurons terminating in the islets, nor do sufficient levels of dopamine circulate through the blood stream. However, L-DOPA does circulate in the blood stream at appropriate levels, and 2-cells contain the molecular machinery needed to convert L-DOPA to dopamine. 2- cells also express the D2 receptor and VMAT-2, which loads dopamine into secretory granules. Thus, a link may exist between D2 receptor inhibition and 2-cell dysfunction, but investigations of this link will depend on a more complete understanding of dopamine action in the 2-cell. Towards this understanding, we hypothesize that 2-cells take up L-DOPA, synthesize dopamine and package it in the insulin secretory granules, and that stimulated secretion of dopamine acts through an autocrine loop to down-regulate subsequent insulin secretion. To test this hypothesis, we will utilize state-of-the-art live cell imaging methods, many of which have been pioneered by our laboratory. These novel techniques allow us to examine intracellular and multicellular events with unprecedented specificity and resolution. We have also developed several novel microfluidic devices for the study of pancreatic islets and their secreted products, and these can all be coupled with our unique quantitative imaging approaches to provide an ideal platform for many of the proposed experiments. In this proposal, we will refine and extend our established live cell imaging approaches to address the following four specific aims: 1) to determine the effects of L-DOPA on 2-cells in terms of the generation of dopamine and resulting modulation of the intracellular signaling pathways involved in GSIS; 2) to determine the intracellular signaling pathways and functional targets of dopamine receptor activation in the 2-cell; 3) to determine the role of expression and trafficking of the D2 receptor and the dopamine transporter in these signaling pathways; 4) to determine the effects of various second generation antipsychotic drugs on these pathways.

描述（由申请人提供）：项目摘要这项研究的长期目标是确定多巴胺信号传导对Langerhans胰岛激素分泌的机制和影响。血糖稳态取决于胰岛2细胞中葡萄糖刺激的胰岛素分泌（GSI），但我们也知道非葡萄糖信号对于调节胰岛素的分泌很重要，并且许多这些信号都通过G蛋白辅助受体进行通信。多巴胺通过多种G蛋白偶联受体起作用，但其在2细胞中的信号传导尚未得到充分表征。所有当前的抗精神病药都阻止了D2多巴胺受体以及其他靶标，而最有效的第二代抗精神病药会导致明显的代谢副作用，从而增加了肥胖和糖尿病风险的增加。不幸的是，关于副作用的分子机制尚无共识。由于所有这些抗精神障碍物D2受体都具有明显的代谢副作用，因此已经假定副作用是由与D2受体以外的分子相互作用介导的。 2细胞很少引起这些药物的潜在靶标，这大概是因为没有已知的多巴胺能神经元在胰岛中终止，也没有足够水平的多巴胺通过血流循环。但是，L-DOPA确实在适当水平的血液中循环，并且2细胞包含将L-DOPA转换为多巴胺所需的分子机械。 2-细胞还表达D2受体和VMAT-2，将多巴胺载入分泌颗粒。因此，D2受体抑制与2细胞功能障碍之间可能存在联系，但是对该链接的研究将取决于对2细胞中多巴胺作用的更完整的理解。为了理解这种理解，我们假设2个细胞占L-DOPA，合成多巴胺并将其包装在胰岛素分泌颗粒中，并且通过自分泌循环刺激了多巴胺的分泌，以下调随后的胰岛素分泌。为了检验这一假设，我们将利用最先进的活细胞成像方法，其中许多是由我们的实验室开创的。这些新型技术使我们能够以前所未有的特异性和分辨率检查细胞内和多细胞事件。我们还开发了几种新型的微流体设备，用于研究胰岛及其分泌产品，并且这些都可以与我们独特的定量成像方法相结合，为许多提出的实验提供理想的平台。在此提案中，我们将完善并扩展我们已建立的活细胞成像方法，以解决以下四个特定目的：1）确定L-DOPA对多巴胺的产生以及导致对GSIS涉及的细胞内信号传导途径的调节的2个细胞的影响； 2）确定2细胞中多巴胺受体激活的细胞内信号通路和功能靶标； 3）确定D2受体和多巴胺转运蛋白在这些信号传导途径中的表达和运输的作用； 4）确定第二代抗精神病药对这些途径的影响。