Function and Regulation of Islet-associated Macrophages in Obesity and Diabetes

肥胖和糖尿病中胰岛相关巨噬细胞的功能和调节

• 批准号: 8877510
• 负责人: David L Morris
• 金额: $ 10.9万
• 依托单位: INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-05 至 2016-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8877510
• 关键词: Adipose tissue; Apoptosis; Autoimmune Process; Award; Beta Cell; Biology; Cell Line; Cell physiology; Cells; Chemotaxis; Chronic; Coculture Techniques; Complement; Data; Defect; Development; Diabetes Mellitus; Exhibits; Flow Cytometry; Foundations; Functional disorder; Future; Gene Expression Profiling; Glucose; Glucose Intolerance; Goals; Health; Housing; Human; Imaging Techniques; Immune; Immunophenotyping; Indiana; Infiltration; Inflammation; Inflammatory; Insulin; Insulin Resistance; Insulin-Dependent Diabetes Mellitus; Interdisciplinary Study; Islets of Langerhans; Laboratories; Lead; Left; Leukocytes; Liver; Macrophage Activation; Mediating; Mentorship; Metabolic; Metabolic Diseases; Metabolic stress; Metabolism; Modeling; Molecular; Mus; Muscle; Non-Insulin-Dependent Diabetes Mellitus; Obese Mice; Obesity; Pathogenesis; Patients; Pediatric Research; Phenotype; Physiology; Population; Regulation; Research; Research Personnel; Research Training; Risk; Rodent Model; Role; Secretory Cell; Staining method; Stains; System; Testing; Therapeutic; Tissues; Training; Universities; Work; career; career development; cytokine; design; driving force; endoplasmic reticulum stress; impaired glucose tolerance; improved; innovation; insulin secretion; islet; macrophage; medical schools; monocyte; mouse model; programs; research study; response; skills

DESCRIPTION (provided by applicant): The applicant's career goal is to develop a multidisciplinary research program focused on defining how inflammation contributes to the development of metabolic disease. Emerging data from the past decade has revealed that obesity-induced metabolic inflammation is a key driving force in the pathogenesis of Type 2 diabetes mellitus (T2DM). In the adipose tissue, liver, and muscle, it is well recognized that obesity leads to progressive infiltration of activated pro-inflammatory macrophages and other leukocytes that act in concert to induce insulin resistance and metabolic dysfunction. At present, relatively little is known about whether and how islet-associated macrophages contribute to islet inflammation, glucose intolerance, and beta cell dysfunction in T2DM. Furthermore, the phenotype, function, and regulation of islet-associated macrophages during the progression of metabolic inflammation and T2DM have yet to be fully defined, leaving critical gaps in our understanding of the pathogenesis of this serious metabolic disease. The central hypothesis of this application is that obesity-induced metabolic stress causes the accumulation of pro-inflammatory macrophages within the islet that exacerbate beta cell dysfunction in T2DM. To test this hypothesis and to begin to uncover the role of islet-associated macrophages in the progression of T2DM, three Specific Aims are proposed. Aim 1 will determine the immunophenotype and inflammatory profile of islet-associated macrophages during the progression of glucose intolerance and T2DM in mouse models. Aim 2 will define the interplay between beta cell endoplasmic reticulum (ER) stress and recruitment and activation of islet-associated macrophages. Aim 3 will investigate the effects of pro-inflammatory macrophages on beta cell secretory function in obesity and T2DM. The diverse experimental approaches outlined in the research plan will allow the applicant to broaden his diabetes expertise by developing new proficiencies and complementary skill sets in the assessment of beta cell function in mouse models, isolated islets, and commonly used beta cell lines. The applicant will benefit from training in the Basic Diabetes Research Group within the Herman B Wells Center for Pediatric Research at the Indiana University School of Medicine, which houses five laboratories that are committed to understanding the molecular mechanisms that lead to the development of all forms of diabetes mellitus. This new training in islet biology will complement the applicant's previous training in physiology, metabolism, and obesity-induced inflammation. A diverse team of established investigators will oversee the applicant's career development during the award period by contributing intellectually to his research training, providing mentorship, and offering career advice.

描述（由申请人提供）：申请人的职业目标是开发一个多学科研究项目，重点是确定炎症如何促进代谢疾病的发展。过去十年的新数据表明，肥胖引起的代谢炎症是 2 型糖尿病 (T2DM) 发病机制的关键驱动力。在脂肪组织、肝脏和肌肉中，众所周知，肥胖会导致活化的促炎巨噬细胞和其他白细胞进行性浸润，这些白细胞协同作用，诱导胰岛素抵抗和代谢功能障碍。目前，关于胰岛相关巨噬细胞是否以及如何导致 T2DM 中的胰岛炎症、葡萄糖耐受不良和 β 细胞功能障碍，人们知之甚少。此外，代谢性炎症和 T2DM 进展过程中胰岛相关巨噬细胞的表型、功能和调节尚未完全明确，这使得我们对这种严重代谢性疾病发病机制的理解存在重大差距。该申请的中心假设是，肥胖引起的代谢应激导致促炎巨噬细胞在胰岛内积聚，从而加剧 T2DM 中的 β 细胞功能障碍。为了检验这一假设并开始揭示胰岛相关巨噬细胞在 T2DM 进展中的作用，提出了三个具体目标。目标 1 将确定小鼠模型中葡萄糖耐受不良和 T2DM 进展过程中胰岛相关巨噬细胞的免疫表型和炎症特征。目标 2 将定义 β 细胞内质网 (ER) 应激与胰岛相关巨噬细胞的募集和激活之间的相互作用。目标 3 将研究促炎巨噬细胞对肥胖和 T2DM 中 β 细胞分泌功能的影响。研究计划中概述的多样化实验方法将使申请人能够通过在评估小鼠模型、分离胰岛和常用β细胞系中的β细胞功能方面发展新的熟练程度和补充技能来拓宽其糖尿病专业知识。申请人将受益于印第安纳大学医学院赫尔曼·B·威尔斯儿科研究中心基础糖尿病研究小组的培训，该中心设有五个实验室，致力于了解导致所有形式糖尿病发展的分子机制。这种胰岛生物学方面的新培训将补充申请人之前在生理学、新陈代谢和肥胖引起的炎症方面的培训。由成熟的研究人员组成的多元化团队将通过为申请人的研究培训提供智力贡献、提供指导和提供职业建议来监督申请人在获奖期间的职业发展。