Trans-Synaptic Transport of Endogenous Proteins to Label Circuits
Trans-Synaptic Transport of Endogenous Proteins to Label Circuits
批准号:
7994598
负责人:
HOLLIS T. CLINE
金额:
$37.98万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-20 至 2014-04-30
关键词:
AddressAffectAmino AcidsAnimalsAreaAxonBehaviorBehavior ControlBehavioralBiomedical ResearchBrainCarrier ProteinsCellsChildhoodChimera organismCognitiveDiseaseEpilepsyEyeGene ExpressionGenesGeneticGoalsHandImageInjection of therapeutic agentLabelLateral Geniculate BodyLifeMammalsMethodsModelingMolecularNeurodevelopmental DisorderNeurologicNeuronsNeurosciencesPropertyProteinsRadiolabeledReporterRetinaSchizophreniaScientistSeizuresSynapsesTestingThalamic structureTimeTranscription CoactivatorTranscriptional RegulationVisual Cortexautism spectrum disorderbasechemical geneticsexcitatory neuronexperienceflexibilityin vivointerestneural circuitnovelpostsynapticpublic health relevanceradiotracertool
中文摘要
描述(申请人提供):神经科学中的一个基本挑战是确定神经元回路如何控制行为,以及依赖经验的回路变化如何带来可塑性或行为变化。为了解决这一基本挑战,我们必须首先识别功能电路中的突触连接神经元,其次,我们必须在诱导电路和行为改变的条件下可视化活动物中连接的神经元。这将使科学家能够测试神经连接中依赖经验的变化是否是行为变化的基础。我们的计划的目标是开发工具,以可视化和操纵活动物功能回路中与突触相连的神经元。我们建议使用一种独特的策略来实现这一目标,在该策略中,我们识别跨越突触的内源性蛋白质,并使用这些蛋白质将Gal4转录激活因子运送到突触后神经元,在那里它将诱导UAS驱动的报告或感兴趣的基因的放大表达。
与公共健康相关:在完整的大脑中可视化和操纵神经元回路的能力将是理解大脑回路如何影响行为的重大进步。我们建议开发一种新的方法来标记跨突触连接的神经元,该方法适用于活体时移成像。
英文摘要
DESCRIPTION (provided by applicant): A fundamental challenge in neuroscience is to determine how neuronal circuits control behavior and how plasticity, or changes in behavior, is brought about by experience- dependent changes in circuitry. To address this basic challenge we must first identify synaptically-connected neurons within a functional circuit and second, we must be to visualize connected neurons in living animals under conditions in which circuits and behavior are induced to change. This will allow scientists to test whether experience- dependent changes in neuronal connections underlie changes in behavior. The goal of our proposal is to generate tools to visualize and manipulate synaptically-connected neurons within functional circuits in living animals. We propose to accomplish this goal using a unique strategy in which we identify endogenous proteins which cross synapses and use these proteins to transport the gal4 transcriptional activator into postsynaptic neurons, where it will induce amplified expression of UAS-driven reporters or genes of interest.
PUBLIC HEALTH RELEVANCE: The ability to visualize and manipulate neuronal circuits in the intact brain is a will be a major advance in understanding how brain circuits affect behavior. We propose to develop a novel method to label trans-synaptically connected neurons which is amenable to in vivo time-lapse imaging.
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