Role of Insulin-like Signaling in Glial Responses to Axon Degeneration

胰岛素样信号传导在神经胶质细胞对轴突变性反应中的作用

• 批准号: 8823836
• 负责人: Mary Allison Logan
• 金额: $ 32.64万
• 依托单位: OREGON HEALTH & SCIENCE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-05-01 至 2016-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8823836
• 关键词: Acute; Adult; Affect; Alzheimer' s Disease; Amyotrophic Lateral Sclerosis; Autoimmune Diseases; Axon; Axotomy; Behavior; Binding; Biological Assay; Brain; Brain region; Cells; Chronic; Chronic Disease; Communication; Complex; Cues; Development; Disease; Drosophila genus; Employee Strikes; Ensure; Event; Gene Expression; Genes; Genetic; Genetic Transcription; Goals; Health; Immune; Immune response; Injury; Insulin; Invaded; Laboratories; Ligands; Link; Mediating; Mission; Molecular; Molecular Genetics; Morphology; Multiple Sclerosis; Nerve Degeneration; Neurodegenerative Disorders; Neuroglia; Neurologic; Neurons; Parkinson Disease; Pathway interactions; Peptides; Proteins; Public Health; Reaction; Receptor Signaling; Recruitment Activity; Role; Signal Pathway; Signal Transduction; Site; Somatomedins; Stress; System; Translations; Trauma; United States National Institutes of Health; Up-Regulation; Vertebrates; Work; axon injury; axonal degeneration; base; central nervous system injury; fly; gene function; genetic manipulation; in vivo; in vivo Model; innate immune function; insight; migration; mutant; nerve injury; nervous system disorder; novel; receptor; receptor coupling; response; response to injury; targeted treatment; temporal measurement; therapeutic target; therapy development; tool

DESCRIPTION (provided by applicant): Glial cells respond potently to neuronal damage, as well as neurodegenerative disease, by displaying overt changes in morphology, gene expression, migration, and phagocytic activity. Dysfunctional responses contribute to the progression of devastating neurological diseases, such as Alzheimer's disease and Parkinson's disease, and can also promote the onset of some autoimmune disorders. Despite the importance of glia in defending brain health, remarkably little is known about the molecular underpinnings of responses to neuronal damage. A vital long-term goal is to understand how basic glial immune reactions are triggered in the adult brain in response to damaged and dying neurons. The core cellular events (e.g. glial migration to injury sites and phagocytic clearance of neuronal debris) are highly conserved across species and recent work is revealing striking molecular conservation, as well. This proposal uses a well- established adult axotomy assay in Drosophila to investigate the molecular features of glial reactions; the fly offers a tractable genetic system to manipulate gene expression and function with exquisite cellular and temporal precision in vivo. Our preliminary work has identified a novel role for the evolutionarily conserved Insulin/insulin-like growth factor (IGF)-Like Signaling (ILS) pathway in orchestrating glial reactions to axon injury. Based on our findings, we hypothesize that ILS regulates glial immune responses in two fundamental ways: (1) Basal ILS activity in adult glia ensures that glia express key genes (i.e. the Draper receptor and adaptor Ced-6) required to detect and carry out responses to axon damage, and (2) Acute activation of the ILS pathway at injury sites triggers rapid responses in local glia to ensure that damaged neurons are cleared from the CNS. This proposal will employ powerful genetic-molecular tools to investigate how the ILS pathway contributes to axotomy-induced functions in glia. We will: (Aim 1) define the role of Insulin-like Receptor (InR) activity in each step of the glial response to axotomy, including altered gene expression, glial recruitment to injury sites, and glial phagocytic activity; (Aim 2) determine how insulin-like peptides (ilps), the InR ligands, influence basal expression of Draper and Ced-6, as well as each step of the injury response in local glia; and (Aim 3) define the molecular signaling cascades downstream of InR that are coupled to these important glial responses. This work will provide critical mechanistic insight into how damaged neurons communicate with glia to elicit responses and elucidate intrinsic molecular pathways that control these essential glial functions. Our findings will also offer a novel framework for exploring ILS components as therapeutic targets to treat CNS injury, as well as chronic neurodegenerative conditions.

描述（由申请人提供）：神经胶质细胞通过表现出明显的形态学、基因表达、迁移和吞噬活性变化，对神经元损伤和神经退行性疾病有强烈的反应。功能失调的反应有助于破坏性神经系统疾病的发展，如阿尔茨海默病和帕金森病，也可以促进一些自身免疫性疾病的发生。尽管神经胶质在保护大脑健康方面很重要，但对神经元损伤反应的分子基础知之甚少。一个重要的长期目标是了解成人大脑中受损和死亡神经元的基本神经胶质免疫反应是如何触发的。核心细胞事件（如神经胶质向损伤部位的迁移和吞噬清除）