Adipose Tissue Macrophage Phenotype and Function

脂肪组织巨噬细胞表型和功能

• 批准号: 7996770
• 负责人: Anthony W Ferrante
• 金额: $ 9.5万
• 依托单位: COLUMBIA UNIVERSITY HEALTH SCIENCES
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-12-17 至 2011-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7996770
• 关键词: Acute-Phase Proteins; Adhesions; Adipocytes; Adipose tissue; Atherosclerosis; Attenuated; Biological; Cells; Chemotaxis; Coagulants; Colony-Stimulating Factors; Data; Development; Endothelium; Functional disorder; Genetic; Giant Cells; Grant; Hematopoietic; Human; Hypertrophy; Inflammation; Inflammatory; Inflammatory Response; Insulin Resistance; Integrins; Intercellular adhesion molecule 1; Literature; Liver diseases; Macrophage Activation; Macrophage Colony-Stimulating Factor Receptor; Malignant Neoplasms; Measures; Mediating; Metabolic; Modeling; Molecular; Monitor; Monocyte Chemoattractant Proteins; Mus; Myelogenous; NF-kappa B; Obese Mice; Obesity; Phenotype; Physiology; Process; Production; Proteins; Recruitment Activity; Research Personnel; Rodent; Signal Transduction; Testing; Transgenic Mice; Vascular Cell Adhesion Molecule-1; Work; capillary bed; chemokine; design; energy balance; fMet-Leu-Phe receptor; improved; insight; insulin sensitivity; macrophage; migration; monocyte; non-alcoholic fatty liver; novel strategies; programs; receptor; research study; success; therapeutic target

DESCRIPTION (provided by applicant): Obesity induces an inflammatory response that has been implicated in the development of medically important complications, including atherosclerosis, insulin resistance, non-alcoholic fatty liver disease and cancer. Studies supported by this grant have revealed a previously unrecognized component of obesity- induced inflammation: adipose tissue macrophages (ATMs). Our work has demonstrated that ATMs accumulate in adipose tissue in proportion to adiposity in both rodents and humans. We have also shown that ATMs are responsible for elaborating proinflammatory, pro-coagulant and acute phase proteins implicated in obesity-induced complications. Through use of mice deficient in a chemoattractant receptor, we have decreased macrophage content in adipose tissue and concomitantly improved the metabolic profile of obese mice. Studies stimulated by our findings have demonstrated that ATM content in humans is tightly correlated with adiposity, insulin sensitivity and powerfully decreased by thiazolidiniones. A more detailed characterization of the process that regulates macrophage accumulation and activation in adipose tissue will provide important insights into the pathophysiology of obesity and its complications, and also provide candidate therapeutic targets. Two basic hypotheses motivate the experiments described in this application: (A) In obesity macrophage accumulation in adipose tissue is a multi-step process that consists of three steps: recruitment, maturation/differentiation and activation. (B) Activated adipose tissue macrophages contribute to the adverse local and systemic inflammatory effects of obesity . In other biological settings the recruitment, differentiation and activation of macrophages have been well characterized. Our specific aims are: (1) To characterize obesity-induced recruitment of monocytes to adipose tissue. (2) To determine whether M-CSF/CSF-1 regulates adipose tissue macrophage differentiation. (3) To determine whether obesity-induced adipose tissue inflammation is dependent upon macrophage NF-kB activation. The specific aims of the current application are designed to identify mechanisms involved in eacg step of macrophage accumulation, and measure the contribution of each to the local and systemic inflammation induced by obesity. In this proposal we have taken advantage of the rich literature that describes macrophage physiology and our preliminary data to propose molecular mechanisms required for recruitment, differentiation and activation of ATMs. Achieving these specific aims of this proposal will identify critical processes and molecules required for ATM accumulation. Success also will provide important insights into adipose tissue physiology, and by identifying the molecular mechanisms that regulate macrophage accumulation and activation in adipose tissue, identify potential novel strategies to reduce obesity-induced inflammation and its attendant complications.

描述（由申请人提供）：肥胖诱导炎症反应，其与医学上重要的并发症的发展有关，包括动脉粥样硬化、胰岛素抵抗、非酒精性脂肪肝和癌症。这项资助支持的研究揭示了一种以前未被认识到的肥胖诱导炎症的成分：脂肪组织巨噬细胞（ATM）。我们的工作表明，ATM在啮齿动物和人类的脂肪组织中的积累与肥胖成比例。我们还表明，ATM负责制定促炎，促凝血和急性期蛋白质参与肥胖引起的并发症。通过使用缺乏化学引诱物受体的小鼠，我们降低了脂肪组织中的巨噬细胞含量，并同时改善了肥胖小鼠的代谢特征。由我们的发现刺激的研究表明，人体中ATM含量与肥胖、胰岛素敏感性密切相关，并被噻唑烷酮类药物有力地降低。更详细的表征过程中，调节巨噬细胞的积累和激活的脂肪组织将提供重要的见解肥胖症的病理生理学及其并发症，也提供了候选的治疗目标。两个基本假设激发了本申请中描述的实验：（A）在肥胖症中，脂肪组织中的巨噬细胞积累是一个多步骤过程，其由三个步骤组成：募集、成熟/分化和活化。(B)激活的脂肪组织巨噬细胞有助于肥胖的不良局部和全身炎症效应。在其他生物学环境中，巨噬细胞的募集、分化和活化已经得到很好的表征。我们的具体目标是：（1）表征肥胖诱导的单核细胞向脂肪组织的募集。(2)确定M-CSF/CSF-1是否调节脂肪组织巨噬细胞分化。(3)确定肥胖诱导的脂肪组织炎症是否依赖于巨噬细胞NF-κ B活化。本申请的具体目的被设计为鉴定参与巨噬细胞积累的每个步骤的机制，并测量每个步骤对肥胖诱导的局部和全身炎症的贡献。在这个提议中，我们利用了描述巨噬细胞生理学的丰富文献和我们的初步数据，提出了ATM募集、分化和激活所需的分子机制。实现本提案的这些具体目标将确定ATM积累所需的关键过程和分子。成功还将为脂肪组织生理学提供重要的见解，并通过确定调节脂肪组织中巨噬细胞积累和激活的分子机制，确定潜在的新策略，以减少肥胖诱导的炎症及其伴随的并发症。