Mechanisms of hematopoietic stem cell activation in obesity

肥胖造血干细胞激活机制

• 批准号: 9459438
• 负责人: Kanakadurga Singer
• 金额: $ 0.15万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-09-01 至 2019-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9459438
• 关键词: Adipose tissue; Age; American; Animal Model; Area; Asthma; Atherosclerosis; Autoimmune Process; Basic Science; Biological Assay; Blood; Bone Marrow; Bone Marrow Cells; Bone Marrow Transplantation; C-reactive protein; Cardiovascular Diseases; Cell Compartmentation; Cell Differentiation process; Cells; Cellular biology; Child; Childhood; Chimera organism; Cholesterol; Chronic; Clinical; Collaborations; Complex; Data; Development; Developmental Biology; Diabetes Mellitus; Diet; Dietary Fatty Acid; Disease; Doctor of Philosophy; Endocrinologist; Endocrinology; Energy Intake; Environment; Epidemic; Evaluation; Event; Expenditure; Fatty Acids; Fatty acid glycerol esters; Functional disorder; Funding; Future; Gender; Generations; Goals; Health; Hematopoiesis; Hematopoietic; Hematopoietic System; Hematopoietic stem cells; High Fat Diet; Human; Hypertension; IL6 gene; ITGAX gene; Immune; Immunology; In Vitro; Individual; Inflammation; Inflammatory; Inflammatory Response; Insulin Resistance; Intervention; Knockout Mice; Knowledge; Lead; Leukocytes; Link; Liver diseases; Macrophage Activation; Malignant Neoplasms; Mediating; Mentors; Mentorship; Metabolic; Metabolic Diseases; Metabolic syndrome; Metabolism; Michigan; Modeling; Morbidity - disease rate; Myelogenous; Myeloid Cells; Myeloid Progenitor Cells; Myelopoiesis; Nutritional; Obese Mice; Obesity; Obesity associated disease; Overnutrition; Pathologic; Pathway interactions; Physicians; Prevention; Process; Production; Publications; Race; Research; Research Personnel; Research Proposals; Role; Saturated Fatty Acids; Scientist; Signal Pathway; Signal Transduction; Source; Stem cells; Supervision; TLR4 gene; TNF gene; Testing; Therapeutic; Thinness; Tissues; Training; Transplantation; United States; Universities; Unsaturated Fatty Acids; Visceral; base; career; cytokine; diabetic; glucose metabolism; in vivo; inflammatory marker; lipid metabolism; macrophage; medical schools; monocyte; mouse model; neutrophil; novel; nutrient metabolism; obesity in children; obesity treatment; progenitor; public health relevance; skills; stem cell biology; stem cell population; success

 DESCRIPTION (provided by applicant): Obesity is increasingly prevalent in the United States. The cellular dynamics that lead from energy intake to complications such as metabolic syndrome are complex and include the activation of inflammatory cells (metainflammation). Increased myeloid (monocyte, neutrophil, macrophage) inflammation in adipose tissue with obesity as well as an increase in circulating monocytes contributes to the development of metabolic and cardiovascular diseases, but the origins of this inflammation are not well understood. Advancing this research question requires an individual uniquely trained in understanding the interface between inflammation and metabolism. The applicant is a Pediatric Endocrinologist who actively treats obese diabetic and pre-diabetic children. To become a physician-scientist with expertise in metainflammation, the candidate will accomplish the following training goals: 1) To further develop expertise in the use of mouse models of obesity to assess glucose and lipid metabolism. 2) To develop expertise in the assessment of hematopoietic stem cells (HSC) and paradigms of experimental immunology in mouse models. 3) To develop the skills necessary to lead an independent basic science research lab, which includes hiring and supervision of technicians and mentoring trainees in the lab. 4) To develop into a successful independent physician scientist, as evidenced by successful collaborations, presentations, publications, and success with independent funding. To accomplish these goals, Dr. Singer has gathered a group of experts in metabolism (Carey Lumeng MD PhD), immunology and cell and developmental biology of HSCs (Doug Engel PhD and Ivan Maillard MD PhD) to oversee this training. Accomplishing this training will facilitate the long-term career goal of becoming an independent investigator with expertise in inflammation and metabolic syndrome in the context of pediatric obesity. The environment at the University of Michigan Medical School is uniquely suited to facilitate this plan through its research centers in diabetes, obesity, and stem cell biology. The scientific goals of this proposal are to investigate the centra hypothesis that diet-induced obesity leads to innate alterations in HSCs promoting myeloid differentiation, and promoting production of inflammatory macrophages that contribute to tissue specific inflammation. The rationale for this direction is based on preliminary observations that hematopoietic stem cells are increased and skewed towards myeloid progenitors with obesity. This research proposal is significant as it has the capacity to identify novel regulated steps in metainflammation along with providing novel areas for intervention in obesity-associated diseases. The specific scientific aims of this proposal are 1) To identify the dietary fatty acids that augment long term hematopoietic stem cell myeloid differentiation during obesity. Aim 2) To determine the role of toll-like receptor 4 in obesity-induced activation of HSCs. Completion of these scientific aims will provide the training required to gain expertise in stem cell assessments, generation and analysis of bone marrow chimeras, and evaluation of nutrient metabolism in mouse models of obesity. The guidance provided by experts in obesity-induced inflammation and hematopoietic stem cell biology will maximize the potential for the applicant to be a successful physician scientist at the interface between these fields.

 描述（由申请人提供）：肥胖在美国越来越普遍。从能量摄入到代谢综合征等并发症的细胞动力学是复杂的，包括炎症细胞的激活（后炎症）。肥胖症患者脂肪组织中髓样（单核细胞、中性粒细胞、巨噬细胞）炎症的增加以及循环单核细胞的增加有助于代谢和心血管疾病的发展，但这种炎症的起源尚不清楚。推进这一研究问题需要一个在理解炎症和代谢之间的界面方面受过独特训练的人。申请人是积极治疗肥胖糖尿病和糖尿病前期儿童的儿科内分泌学家。为了成为一名具有代谢炎症专业知识的医生科学家，候选人将完成以下培训目标：1）进一步发展使用肥胖小鼠模型评估葡萄糖和脂质代谢的专业知识。2)发展造血干细胞（HSC）评估和小鼠模型实验免疫学范例的专业知识。3)培养领导独立的基础科学研究实验室所需的技能，包括雇用和监督实验室的技术人员和指导实习生。4)发展成为一个成功的独立医生科学家，通过成功的合作，演讲，出版物和独立资助的成功证明。为了实现这些目标，Singer博士召集了一组代谢（Carey Lumeng MD PhD），免疫学以及HSC细胞和发育生物学（Doug Engel PhD和Ivan Maillard MD PhD）的专家来监督这项培训。完成这项培训将有助于实现长期的职业目标，即成为一名在儿童肥胖症背景下具有炎症和代谢综合征专业知识的独立研究者。密歇根大学医学院的环境非常适合通过其糖尿病研究中心促进这一计划， 肥胖和干细胞生物学。该提案的科学目标是研究中心假说，即饮食诱导的肥胖导致HSC的先天改变，促进骨髓分化，并促进炎症巨噬细胞的产生，从而导致组织特异性炎症。这一方向的基本原理是基于初步观察，即造血干细胞增加并偏向于肥胖的骨髓祖细胞。这项研究计划是重要的，因为它有能力确定新的调节步骤，在metainflammation沿着与提供新的领域，干预肥胖相关疾病。该提案的具体科学目的是1）鉴定在肥胖期间增强长期造血干细胞髓样分化的膳食脂肪酸。目的2）探讨Toll样受体4在肥胖诱导的肝星状细胞活化中的作用。这些科学目标的完成将提供获得干细胞评估、骨髓嵌合体的生成和分析以及肥胖小鼠模型营养代谢评估方面的专业知识所需的培训。由肥胖引起的炎症和造血干细胞生物学专家提供的指导将最大限度地提高申请人成为这些领域之间的成功医生科学家的潜力。