grant

The Influence of the Pretectum on the Pulvinar Nucleus

Organization UNIVERSITY OF LOUISVILLELocation LOUISVILLE, UNITED STATESPosted 1 Jan 2025Deadline 31 Dec 2027
NIHUS FederalResearch GrantFY20262-photonAddressAffectAmblyopiaAnimalsAxon TerminalsBrainBrain Nervous SystemCRE RecombinaseCalcium Ion SignalingCalcium SignalingCatsCats MammalsCell BodyCell Communication and SignalingCell NucleusCell SignalingCellsCodeCoding SystemDarknessDendritesDiagnosisDiseaseDisorderDomestic CatsDyslexiaElectron MicroscopyEncephalonEnterobacteria phage P1 Cre recombinaseEnvironmentExhibitsEye Motility DisordersEye Movement DisordersEye MovementsFeline SpeciesFelis catusFelis domesticaFelis domesticusFelis sylvestris catusFiber OpticsFluorescenceFrequenciesGlutamatesGoalsHSVHeadHerpes Simplex VirusHerpes labialis VirusImageIn VitroIndividualInjectionsIntracellular Communication and SignalingKnowledgeL-GlutamateLaser ElectromagneticLaser RadiationLasersLightLinkMedicalMethodsMiceMice MammalsModelingMorphologyMotionMovementMurineMusNasalNasal Passages NoseNerve CellsNerve UnitNeural CellNeurocyteNeuronsNoseNucleusOcular Motility DisordersOpsinParvalbuminsPathologic NystagmusPathway interactionsPatternPhoriasPhotic StimulationPhotoradiationPhysiologic pulsePlasma Retinol-Binding ProteinPresynaptic Nerve EndingsPresynaptic TerminalsPrimary visual cortexProbabilityPropertyProtocolProtocols documentationPulsePulvinarPulvinar structureRBP4RBP4 geneRabies mappingRabies trans synaptic tracingRabies virus mediated mappingReactionReflexReflex actionReporterResearchRespiratory System, Nose, Nasal PassagesRetinaRetinal Ganglion CellsRetinol-Binding Protein 4Rod-OpsinRoleRunningSaccadesSaccadic Eye MovementsSaccadic PursuitSchizophreniaSchizophrenic DisordersShapesSightSignal TransductionSignal Transduction SystemsSignalingSimplexvirusSourceSpeedSquintStimulusStrabismusStriate CortexStriate areaStructureSynapsesSynapticSynaptic BoutonsSynaptic TerminalsTestingThalamic structureThalamusViralVirusVisionVisualVisual FieldsVisual MotionVisual StimulationWhole-Cell RecordingsWord Blindnessactive visionarea striataawakebacteriophage P1 recombinase Crebiological signal transductionbody movementcatscell typedementia praecoxeye fieldeye trackingfluorescence imagingfluorescent imaginggazeglutamatergicimagingin vivoinsightneuronalnystagmusoptogeneticspathwaypreferencepulvinar thalamirabies based mappingrabies based retrograde mappingrabies circuit tracingrabies mediated retrograde monosynaptic tracingrabies retrograde tracingrabies tracerrabies tracingrabies viral tracingrabies virus mediated circuit mappingrabies virus monosynaptic circuit tracingrabies virus monosynaptic tracingrabies virus neurotracerrabies virus retrograde tracingrabies virus tracingresponseretinal ganglionschizophrenicsocial rolespatial and temporalspatial temporalspatiotemporalsynapsethalamictooltracing with rabiestwo-photonvisual functionvisual stimulusvisual tracking
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Full Description

Project Summary
To accurately code and react to the visual environment, signals from the retina must integrate with the spatial

and temporal aspects of eye and body movements. Projections from the pretectum (PT) to the pulvinar

nucleus (PUL) may serve in modifying visual signals in the context of eye and/or body movements. However,

the specific role of the PT in active vision has not been tested using precise circuity manipulation methods. In

the mouse, projections from the PT innervate rostral regions of the PUL that are reciprocally connected to

the primary visual cortex (V1). However, little is currently known regarding PT and rostral PUL circuits, or

how manipulation of the PT modifies rostral PUL activity. I propose to address these gaps in knowledge via

the following specific aims. Aim 1) Determine the ultrastructure, synaptic properties, and convergence

patterns of layer 5 V1 and PT inputs to rostral PUL neurons using viral tracing, electron microscopy, in vitro

recording, and optogenetics. Aim 2) Characterize the morphology and response properties of retinal ganglion

cells that innervate PT-PUL neurons using combinations of herpes simplex virus retrograde tracing,

monosynaptic rabies virus tracing, and in vitro two-photon fluorescence imaging of calcium signals. Aim 3)

Determine the response properties of PT neurons and how they affect the visual response properties of

rostral PUL neurons by combining in vivo recordings from the PT and PUL of awake head-fixed mice with

optogenetic inhibition of PT neurons. The goal of this project is to test the overarching hypothesis that the PT

modulates PUL visual signals in the context of animal movement.

Grant Number: 5F31EY036691-02
NIH Institute/Center: NIH

Principal Investigator: Howard Boone

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