Mechanisms of Viral-Induced Beta Cell Damage

病毒引起的 β 细胞损伤的机制

• 批准号: 8013835
• 负责人: JOHN A CORBETT
• 金额: $ 37.24万
• 依托单位: MEDICAL COLLEGE OF WISCONSIN
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-02-01 至 2013-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8013835
• 关键词: Address; Animal Model; Antigens; Antiviral Agents; Antiviral Response; Apoptosis; Autoimmune Diseases; Beta Cell; Biochemical; Biological Models; Cell Death; Cell Survival; Cell physiology; Cell surface; Cells; Development; Diabetes Mellitus; Disease; Dose; Double-Stranded RNA; Encephalomyocarditis virus; Endocrine; Event; Gene Expression; Genes; Genetic Predisposition to Disease; Genome; Goals; Human; Infection; Inflammation; Inflammatory; Inflammatory Response; Insulin; Insulin-Dependent Diabetes Mellitus; Interferons; Interleukin-1; Islets of Langerhans; Lead; Lymphocyte; Macrophage Activation; Mediating; Mediator of activation protein; Molecular; Mus; Necrosis; Nitric Oxide; PTGS2 gene; Pathway interactions; Poly I-C; Prevention; Production; Published Comment; RNA; RNA Viruses; Rattus; Receptor Signaling; Regulation; Research; Signal Pathway; Source; Stimulus; Structure; Suggestion; Techniques; Testing; Therapeutic; Transgenic Organisms; Translating; Translational Research; Translations; Viral; Virus; Virus Diseases; base; cell injury; cytokine; design; human disease; insight; islet; macrophage; novel; receptor; research study; response

DESCRIPTION (provided by applicant): Insulin-dependent diabetes mellitus (IDDM) is an autoimmune disease that is characterized by selective destruction of insulin secreting beta-cells found in pancreatic islets of Langerhans. Viral infection is one event proposed to initiate beta-cell damage during the development of this disease. While recent studies have begun to unravel the mechanisms by which virus infection modulates the lymphocytic response, few studies have examined the impact of virus infection on macrophage activation or the direct effects of virus infection on beta-cell function and viability. The broad goals of this research are to elucidate the biochemical mechanisms by which virus infection regulates macrophage activation and to determine the virus-activated pathways that contribute to the loss of beta-cell function and viability. Using a virus known to induce diabetes in susceptible mice, we have recently identified three novel antiviral signaling pathways that regulate inflammatory gene expression in macrophages. In response to a virus infection, the fate of beta-cells appears to be dependent on the response elicited, where an inflammatory response appears to result in beta-cell necrosis, and in the absence of inflammation beta-cell apoptosis ensues. There are two specific aims: 1. To test the hypothesis that the activation state of PI3K determines the response of macrophages to virus infection. When PI3K is in an activated state, virus infection stimulates the expression of inflammatory genes such as IL-1, iNOS and COX-2. When inhibited, virus infection induces macrophage apoptosis. 2. To elucidate the pathways responsible for regulating the response of beta-cells to a virus infection. Specific experiments will determine the mechanisms by which virus infection stimulates inflammatory gene expression by beta-cells, and the pathways and determinants that are responsible for beta-cell death, either by necrosis or apoptosis. A number of biochemical, molecular, immunological, histochemical, and transgenic techniques will be utilized to investigate the cellular pathways through which viral infection stimulates macrophage activation and modulates beta-cell function and viability. It is hoped that insights into regulation of macrophage and beta-cell responses to virus infection gained from these proposed studies will influence the design of therapeutic strategies aimed at the prevention of this debilitating disease.

描述（由申请人提供）：胰岛素依赖型糖尿病（IDDM）是一种自身免疫性疾病，其特征是选择性破坏胰岛中发现的胰岛素分泌β细胞。病毒感染是在该疾病发展过程中引发β细胞损伤的一种事件。虽然最近的研究已经开始解开病毒感染调节淋巴细胞反应的机制，但很少有研究检查病毒感染对巨噬细胞活化的影响或病毒感染对β细胞功能和活力的直接影响。本研究的广泛目标是阐明病毒感染调节巨噬细胞活化的生化机制，并确定导致β细胞功能和活力丧失的病毒活化途径。使用已知在易感小鼠中诱导糖尿病的病毒，我们最近确定了三种调节巨噬细胞中炎症基因表达的新型抗病毒信号通路。在对病毒感染的应答中，β细胞的命运似乎取决于引发的应答，其中炎性应答似乎导致β细胞坏死，并且在没有炎症的情况下导致β细胞凋亡。有两个具体目标：1。为了检验PI 3 K的活化状态决定巨噬细胞对病毒感染的反应的假设。当PI 3 K处于激活状态时，病毒感染刺激炎性基因如IL-1、iNOS和考克斯-2的表达。当被抑制时，病毒感染诱导巨噬细胞凋亡。 2.为了阐明负责调节反应的途径， 病毒感染的β细胞具体的实验将确定病毒感染刺激β细胞表达炎症基因的机制，以及负责β细胞死亡（坏死或凋亡）的途径和决定因素。许多生物化学、分子、免疫学、组织化学和转基因技术将被用来研究病毒感染刺激巨噬细胞活化和调节巨噬细胞增殖的细胞途径。 β细胞功能和活力。希望从这些拟议的研究中获得的对巨噬细胞和β细胞对病毒感染的反应的调节的见解将影响旨在预防这种使人衰弱的疾病的治疗策略的设计。