Neural Circuits and Function in Primary Visual Cortex
Neural Circuits and Function in Primary Visual Cortex
批准号:
7323661
负责人:
EDWARD M CALLAWAY
金额:
$47.88万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-09-01 至 2012-06-30
关键词:
Action PotentialsAddressAmblyopiaAnimalsAntibodiesAppendixAreaAxonBrainCell NucleusCellsCerebral cortexChildhoodChromosome PairingCodeComplexDendritesDorsalDyesDyslexiaEyeFunctional disorderGenesGenomeGlycoproteinsGoalsGreen Fluorescent ProteinsHelper VirusesHeterogeneityHumanIn VitroIndividualInfectionInjection of therapeutic agentKnowledgeLabelLaboratoriesLinkLocationMacacaMediatingMethodsMonkeysMorphologyNeuronsNumbersOcular PhysiologyOutputPathway interactionsPresynaptic TerminalsPrimatesPrincipal InvestigatorProcessProgress ReportsPropertyPublishingPulvinar structureRabiesRabies virusRetinaRetinalRetinal ConeRetinal Ganglion CellsSiteSliceSourceStaining methodStainsStimulusStrabismusStructureSynapsesSystemThalamic structureTimeTissue StainsTissuesTracerTravelV1 neuronViralVirusVisionVisualVisual CortexVisual PerceptionVisual system structureWorkarea MTarea striatabasecell typecomputerizedexcitatory neuronextracellularextrastriatein vivoinhibitory neuronkoniocellularlanganiteneural circuitneuron componentneuronal cell bodynovelreceptive fieldresearch studyresponsespatiotemporalsuperior colliculus Corpora quadrigeminatoolvisual informationvisual processvisual processingvisual stimulus
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Visual perception is mediated by complex interactions amongst neurons in the retina, visual cortex, and subcortical brain structures. The importance of vision to humans and other primates is reflected in the enormous percentage of cerebral cortex devoted to processing visual information. Thus, deficits in visual processing are particularly debilitating and arise from abnormalities not only in the eye, but also in cortical circuitry. For example, strabismus or amblyopia during childhood can have long-lasting effects on the cortical circuits that process visual information. There is also evidence that some forms of dyslexia result from central visual system abnormalities. The proposed studies are aimed at understanding the organization and function of neural circuits to, from, and within the primary visual cortex (V1), with the broader objective of understanding how neural circuits mediate visual perception. In particular, these studies aim to identify: 1) the detailed morphological properties of V1 cell types that project to particular extrastriate visual cortical areas and subcortical structures; 2) the sources of direct local input to V1 neurons with projections to particular extrastriate visual cortical areas and subcortical structures; 3) the retinal ganglion cell types that provide input, via the LGN, to functionally and anatomically distinct compartments in V1; and 4) how the in vivo visual response properties of individual, identified neurons correlate with the connectivity of these same cell types, as revealed by our previous and ongoing in vitro studies. The first 3 goals will be achieved using novel viral circuit tracing tools developed in the principal investigator's laboratory. These tools allow complete filling of identified projection neurons and monosynaptically-restricted transynaptic labeling from specific projection neurons. The last aim is accomplished by recording visual responses of V1 neurons and labeling them with dye to correlate anatomically distinct cell types with function. The proposed studies will allow an unprecedented view of visual cortical circuits - they will reveal the detailed connectivity of neurons in visual cortex and how these circuits relate to the functional properties of the component neurons. Lay summary: Deficits in visual processing are particularly debilitating and arise from abnormalities not only in the eye, but also in cortical circuitry. The proposed studies will reveal the normal organization and function of visual cortical circuits, which is necessary to understand the underlying causes of visual dysfunction.
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会议论文
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批准号:10025622
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项目类别:
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资助金额:$78.98万
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财政年份:2020
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批准号:10237360
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资助金额:$73.19万
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财政年份:2020
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依托单位:
Center for Epigenomics of the Mouse Brain Atlas (CEMBA)
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批准号:9568015
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资助金额:$480.55万
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财政年份:2017
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依托单位:
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批准号:9459190
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项目类别:
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资助金额:$29.1万
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财政年份:2017
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负责人:EDWARD M CALLAWAY
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依托单位:
Center for Epigenomics of the Mouse Brain Atlas (CEMBA)
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项目类别:
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资助金额:$500.85万
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财政年份:2017
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负责人:EDWARD M CALLAWAY
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依托单位:
Center for Epigenomics of the Mouse Brain Atlas (CEMBA)
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批准号:10252523
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项目类别:
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资助金额:$36.19万
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财政年份:2017
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负责人:EDWARD M CALLAWAY
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依托单位:
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项目类别:
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资助金额:$29.56万
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财政年份:2015
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负责人:EDWARD M CALLAWAY
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依托单位:
Robust trans-synaptic labeling technologies for cell type-specific quantitation of synaptic connectivity
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批准号:8935699
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项目类别:
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资助金额:$37.74万
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财政年份:2015
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负责人:EDWARD M CALLAWAY
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依托单位:
Resources for Studying Neural Circuit Structure and Function with G-Deleted Rabies Viruses
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批准号:9130302
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项目类别:
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资助金额:$29.75万
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财政年份:2015
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负责人:EDWARD M CALLAWAY
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依托单位:
Resources for Studying Neural Circuit Structure and Function with G-Deleted Rabies Viruses
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批准号:9310416
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项目类别:
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资助金额:$29.84万
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财政年份:2015
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负责人:EDWARD M CALLAWAY
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依托单位:
Organization and Function of Visual Cortical Feedback Systems
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批准号:10468464
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项目类别:
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资助金额:$4.33万
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财政年份:2012
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负责人:EDWARD M CALLAWAY
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依托单位:
Organization and Function of Mouse Visual Cortical Areas
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批准号:8658100
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项目类别:
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资助金额:$54.74万
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财政年份:2012
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负责人:EDWARD M CALLAWAY
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依托单位:
Organization and Function of Visual Cortical Feedback Systems
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批准号:9750116
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项目类别:
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资助金额:$64.28万
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财政年份:2012
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负责人:EDWARD M CALLAWAY
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依托单位:
Organization and Function of Visual Cortical Feedback Systems
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批准号:10220039
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项目类别:
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资助金额:$52.27万
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财政年份:2012
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负责人:EDWARD M CALLAWAY
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依托单位:
Organization and Function of Visual Cortical Feedback Systems
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批准号:9316389
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项目类别:
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资助金额:$48.5万
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财政年份:2012
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负责人:EDWARD M CALLAWAY
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依托单位:
Organization and Function of Visual Cortical Feedback Systems
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批准号:9979896
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项目类别:
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资助金额:$64.28万
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财政年份:2012
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负责人:EDWARD M CALLAWAY
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依托单位:
Organization and Function of Mouse Visual Cortical Areas
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批准号:8321413
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项目类别:
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资助金额:$55.86万
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财政年份:2012
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负责人:EDWARD M CALLAWAY
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依托单位:
Organization and Function of Mouse Visual Cortical Areas
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项目类别:
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资助金额:$53.06万
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财政年份:2012
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负责人:EDWARD M CALLAWAY
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依托单位:
海外基金