Novel technologies for nontoxic transsynaptic tracing
Novel technologies for nontoxic transsynaptic tracing
批准号:
8935945
负责人:
IAN R WICKERSHAM
金额:
$70.82万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-26 至 2017-05-31
关键词:
AcuteAddressAlzheimer&aposs DiseaseAnimalsAreaBehaviorBehavioralBehavioral ParadigmBrainCognitionCognitiveComplexEngineeringEpilepsyFlow CytometryGene ExpressionGene Expression ProfileGenerationsGenesGeneticHealthHuntington DiseaseImageIn SituIndividualInfectionLabelLeftLentivirus VectorMental disordersModelingMonitorMusNeuronsNeurosciencesParkinson DiseasePhysiologicalPopulationPresynaptic TerminalsPrimatesProblem SolvingRabiesRabies virusRattusReporterResearch PersonnelResolutionRodentRoleSliceSynapsesSystemTechniquesTechnologyTestingTimeToxic effectTransgenesTransgenic OrganismsViralViral GenesViral GenomeViral VectorVirusWhole-Cell Recordingsautism spectrum disorderbasecalcium indicatorenv Gene Productsgenetic technologyin vivokillingsmutantnervous system disorderneural circuitnew technologynoveloperationoptical imagingoptogeneticsparticlerecombinaserelating to nervous systemresearch studytooltransgene expressionvectorvirus envelope
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Genetic tools have dramatically increased the power and resolution of neuroscientific experiments, allowing monitoring and perturbation of specific neuronal populations within the brain, often in the context of complex cognitive and behavioral paradigms. However, the usefulness of these tools is limited by the available means of delivering them in circuit-specific ways, a major drawback in view of the critical importance of specific connectivity between individual neurons and between neuronal classes. The primary available means of achieving transgene expression based on neurons' synaptic connections is virus-based transsynaptic tracing, which allows identification, activity imaging, optogenetic control, and perturbation of gene expression in networks of synaptically connected neurons in vivo. The required viruses, however, are toxic within a few days, precluding longer-term experiments that are needed to address many central questions in neuroscience. We will solve this problem by engineering viral transsynaptic tracing systems with either greatly reduced or entirely eliminated toxicity, so that the role of neuronal networks of known connectivity in cognition and behavior. The result will be a set of tools that will allow optical imaging, physiological recording, and manipulation of the activity and gene expression of neuronal networks of known synaptic connectivity in the context of behavioral and other experimental paradigms lasting weeks, months, or years, in any mammalian model species. This will greatly enhance our understanding of the neural bases of normal cognition as well as neurological and mental disorders.
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