Mechanisms of Synapse Remodeling

突触重塑机制

• 批准号: 8309585
• 负责人: Jihong Bai
• 金额: $ 24.9万
• 依托单位: FRED HUTCHINSON CANCER RESEARCH CENTER
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-22 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8309585
• 关键词: Adhesions; Adolescent; Adult; Afferent Neurons; Alleles; Animals; Antibodies; Axon; Backcrossings; Behavior; Biochemical Reaction; Biological Assay; Biological Models; Brain; C-terminal; Caenorhabditis; Caenorhabditis elegans; Candidate Disease Gene; Capsaicin; Cell Fate Control; Cell Nucleus; Cell division; Cells; Chromosome Mapping; Complement; Complementary DNA; Contracts; Coupled; Cytosol; Data; Defect; Degradation Pathway; Dendrites; Detection; Development; Diffuse; Distant; Dorsal; Drosophila genus; Ecdysone; Ectopic Expression; Electrophysiology (science); Equilibrium; Event; Excision; Exhibits; Future; Gene Expression; Gene Silencing; Genes; Genetic; Genetic Screening; Genome; Glycine; Goals; Gonadal Hormones; Gonadal structure; Hawaiian population; Hippocampus (Brain); Hormones; Hour; Hypothalamic structure; Image; Image Analysis; Immunoblotting; Individual; Instruction; Invertebrates; Lead; Left; Life; Light; Location; Lysine; Maps; Measures; Mediating; Mental disorders; Mentors; Methods; Microarray Analysis; Modeling; Molecular; Monitor; Motor Neurons; Muscle; Mutation; N-terminal; Natural regeneration; Nervous system structure; Neurons; Neuropeptides; Nuclear Hormone Receptors; Nuclear Localization Signal; Optics; Pathway interactions; Pattern; Peptides; Phase; Phenotype; Play; Point Mutation; Potassium Channel; Process; Proprotein Convertases; Proteins; Protocols documentation; RNA Interference; RNAi vector; Reagent; Recruitment Activity; Regulation; Reporter; Reporting; Research; Resistance; Role; Schizophrenia; Screening procedure; Sensory; Side; Signal Pathway; Signal Transduction; Single Nucleotide Polymorphism; Site; Staging; Suppressor Mutations; Synapses; Synaptic Transmission; System; TRPV1 gene; Testing; Therapeutic Intervention; Time; Time Study; Training; Transgenes; Transgenic Animals; Transgenic Organisms; Ubiquitin; Ubiquitination; Update; Visual; Voltage-Gated Potassium Channel; arm; base; blind; cholinergic; daughter cell; density; ecdysone receptor; excitatory neuron; experience; follow-up; gain of function mutation; gene function; hatching; in vivo; inhibitory neuron; interest; knock-down; member; multicatalytic endopeptidase complex; mutant; nervous system disorder; neuroblast; neuronal cell body; novel; novel strategies; overexpression; patch clamp; presynaptic; programs; promoter; protein degradation; protein transport; research study; senescence; synaptic function; synaptogenesis; ubiquitin-protein ligase

Synapse remodeling is the process of forming and eliminating synapses to reorganize the existing brain circuitry, and is indispensable for establishing and maintaining the integrity of the nervous system. Synapses are constantly remodeled throughout the lifetime of an animal. Remodeling peaks in the juvenile nervous system, levels off throughout adulthood, and declines with senescence. The long-term goal of my research is to identify the signaling pathways and molecular machinery that mediate synapse remodeling. This will help us to understand how synapses are formed and eliminated at the right time and right place, and provide fundamental information towards our ultimate goal of understanding and treating numerous neurological diseases and mental disorders. To approach analysis of synapse remodeling at the molecular level, it is informative to begin with a simple invertebrate model. In C. elegans, synapse remodeling occurs in a reliable and predictable manner during development. At the end of the first larval stage, 6 motor neurons reverse their axon-dendrite polarity, disassemble existing synapses, and form new ones in a distant location. This simple rewiring process provides an excellent model system that is accessible to both molecular manipulation and in vivo optical observation. The objective of my proposed research is to investigate the molecular pathways defining the timing of synapse remodeling and to identify new genes involved in switching the identity ofthe synapses. This proposal includes the following aims: first, I will investigate temporal regulation of synapse remodeling, testing the hypothesis that genes responsible for controlling the sequence of developmental events (heterochronic genes) regulate synapse remodeling. Second, I will combine data from microarray analysis, a RNAi screen and a forword genetic screen to identify new factors required for synapse remodeling. Finally, a novel quantitative imaging analysis approach will be used to determine spatial regulation ofthe ubiquitin-proteasome system mediating degradation of synaptic components during synapse remodeling. Together, the experiments outlined in this proposal will provide a mechanistic understanding of svnapse remodelina and its regulation.

突触重塑是形成和消除突触以重组现有大脑的过程 它是神经系统的重要组成部分，是建立和维持神经系统完整性所不可或缺的。突触 在动物的一生中不断地被重塑。幼年神经系统的重塑高峰 系统，在整个成年期趋于平稳，并随着衰老而下降。我研究的长期目标是 以确定介导突触重塑的信号通路和分子机制。这将有助于 我们了解突触是如何形成和消除在正确的时间和正确的地点，并提供 我们的最终目标是了解和治疗许多神经系统疾病， 疾病和精神障碍。为了在分子水平上分析突触重塑， 从一个简单的无脊椎动物模型开始开始。In C. elegans，突触重塑发生在可靠的 在发展过程中的可预测性。在第一幼虫期结束时，6个运动神经元反转 它们的轴突-树突极性，分解现有的突触，并在远处形成新的突触。这 简单的重新布线过程提供了一个极好的模型系统， 操作和体内光学观察。我所提出的研究的目的是调查 定义突触重塑时间的分子途径，并确定参与突触重塑的新基因。 转换突触的身份。这一建议包括以下目的：首先，我将调查 突触重塑的时间调节，测试假设，基因负责控制 发育事件的顺序（异时基因）调节突触重塑。第二，我会 联合收割机从微阵列分析、RNAi筛选和前向遗传筛选中获得的数据来鉴定新的因子 突触重塑所必需的最后，一种新的定量成像分析方法将被用于 确定泛素-蛋白酶体系统介导突触降解的空间调节 突触重塑过程中的成分。总之，本提案中概述的实验将提供一个 对突触重塑及其调控机制的认识。