grant

Functional and Molecular Dissection of Marmoset Face Areas

Organization BOSTON UNIVERSITY (CHARLES RIVER CAMPUS)Location BOSTON, UNITED STATESPosted 1 Jun 2025Deadline 31 May 2027
NIHUS FederalResearch GrantFY20252-photonASDAddressAffectAgnosia for FacesArchitectureAreaAtlasesAutismAutistic DisorderBindingBiologic ModelsBiological ModelsBrainBrain DiseasesBrain DisordersBrain Nervous SystemCalciumCallithrixCallithrix jacchusCallithrix jacchus jacchusCell BodyCellsCommon MarmosetDNA AlterationDNA Sequence AlterationDegenerative Neurologic DisordersDiseaseDisorderDissectionEarly Infantile AutismElementsEncephalonEncephalon DiseasesEndowmentEngineering / ArchitectureExpression SignatureFaceFace ProcessingFacial Recognition AgnosiaFoundationsFunctional ImagingGene CombinationsGene ExpressionGene Expression ProfileGenesGeneticGenetic AlterationGenetic IdentityGenetic MarkersGoalsHapaleHumanImageImaging ProceduresImaging TechnicsImaging TechniquesImpairmentIndividualInfantile AutismIntracranial CNS DisordersIntracranial Central Nervous System DisordersInvestigationJointsKanner's SyndromeLinkMapsMarmosetsMethodsMiceMice MammalsModel SystemModelingModern ManMolecularMolecular InteractionMurineMusNHP modelsNeocortexNerve CellsNerve UnitNervous System Degenerative DiseasesNeural CellNeural Degenerative DiseasesNeural degenerative DisordersNeurocyteNeurodegenerative DiseasesNeurodegenerative DisordersNeurodevelopmental DisorderNeurologic Degenerative ConditionsNeurological Development DisorderNeuronsOptical MethodsOpticsPerceptionPersonal SatisfactionPharmacogeneticsPhotic StimulationPhysiologic ImagingPilot ProjectsPopulationPrimatesPrimates MammalsProcessPropertyProsopagnosiaR-Series Research ProjectsR01 MechanismR01 ProgramResearch GrantsResearch Project GrantsResearch ProjectsResearch ResourcesResearch SpecimenResolutionResourcesRodentRodentiaRodents MammalsRoleSensorySequence AlterationShort-Tusked MarmosetSightSolidSomatosensory CortexSpecimenSurvey InstrumentSurveysSystemTechnologyTissue imagingVisionVisual PerceptionVisual StimulationWorkautism spectral disorderautism spectrum disorderautistic spectrum disorderblindcell typedegenerative diseases of motor and sensory neuronsdegenerative neurological diseasesextrastriate areaextrastriate cortexextrastriate visual cortexface perceptionfacesfacialfacial processinggene biomarkergene expression biomarkergene expression patterngene expression signaturegene manipulationgene markergene panelgene signature biomarkergenetic biomarkergenetic manipulationgenetically manipulategenetically perturbgenomic alterationhomotypical corteximaginginnovateinnovationinnovativeinsightisocortexmulti-modalitymultigene panelmultimodalityneopalliumneural mechanismneurodegenerative illnessneurodevelopmental diseaseneuromechanismneuronalneuronal circuitneuronal circuitryneuropsychiatric diseaseneuropsychiatric disordernonhuman primate modelsobject recognitionoptic imagingopticaloptical imagingoptogeneticsphysiological imagingpilot studypopulation surveyresolutionssocial cognitionsocial rolesomesthetic sensory cortexspatial RNA sequencingspatial gene expression analysisspatial gene expression profilingspatial resolved transcriptome sequencingspatial transcriptome analysisspatial transcriptome profilingspatial transcriptome sequencingspatial transcriptomicsspatially resolved transcriptomicsspatio transcriptomicssupport networktargeted drug therapytargeted drug treatmentstargeted therapeutictargeted therapeutic agentstargeted therapytargeted treatmenttooltranscriptional profiletranscriptional signaturetranscriptomicstwo-photonventral pathwayventral processing streamventral streamventral visual pathwayventral visual processing streamventral visual streamvisual areavisual functionwell-beingwellbeingwhite ear-tufted marmosetwhite-tufted marmoset
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Full Description

PROJECT SUMMARY
Face perception is supported by multiple highly specialized regions, interconnected to form a face-processing

network. Because of the clarity of its functional organization, the system has allowed for unprecedented insights

into the neural mechanisms and computational principles of high-level object recognition at large. These insights

were gained through recordings from face areas that have been blind to the molecular properties of face cells.

Yet the conserved organization of face areas among primates suggest an evolutionary origin in which genetic

alterations may have contributed to circuit-specific innovations in neuronal properties that endowed these areas

with their function. Genes expression patterns differentiate one cortical area or cell type from another.

Understanding the neuronal circuits that underly face processing requires relating the genetic identity of different

face areas and individual face cells to their specific functions. In this project, we propose pilot work to generate

a first-ever, cell-type-specific, functional map of face areas in the primate brain. We will use the common

marmoset, a New World primate model amenable to genetic manipulation and with a lissencephalic brain

accessible for optical imaging. We will leverage newly generated atlases of molecular-defined cell types of the

marmoset brain that will guide the selection of gene panels to survey face areas. We have established methods

that combine functional imaging with post-hoc spatial transcriptomics that allows for dense surveys of population

activity and their subsequent cell-type identification. In Aim 1, we will combine optical intrinsic imaging with

sequencing-based spatial transcriptomics to determine whether the topological arrangement of face patches can

be defined by its molecular architecture. In Aim 2, we will combine population two-photon calcium imaging with

imaging-based spatial transcriptomics to determine whether face-selective cells are defined by specific molecular

cell types. This pilot study will lay the groundwork for the genetic dissection of cortical circuits underlying primate

face processing. This will allow us to unravel the circuit-level computations that give rise to facial perception and

how such processes are altered in neurodevelopmental and neurodegenerative disorders that disrupt social

cognition.

Grant Number: 1R21EY037066-01A1
NIH Institute/Center: NIH

Principal Investigator: Jerry Chen

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