grant

Dopaminergic Control of Glial Cells in Prefrontal Cortex Functions

Organization UNIVERSITY OF CALIFORNIA-IRVINELocation IRVINE, UNITED STATESPosted 5 Sept 2024Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY202521+ years oldAdultAdult HumanAffectAlgorithmsAmericanAntibodiesAntipsychotic AgentsAntipsychotic DrugsAntipsychoticsAstrocytesAstrocytusAstrogliaAstroproteinAutoreceptorsAutoregulationBehaviorBiochemicalBody TissuesBrainBrain DiseasesBrain DisordersBrain Nervous SystemCausalityCell BodyCell Communication and SignalingCell IsolationCell SegregationCell SeparationCell Separation TechnologyCell SignalingCellsChronicCognitiveCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalD2 receptorDRD2 ReceptorDataDendritic SpinesDiagnosisDissectionDisturbance in cognitionDopamineDopamine D2 ReceptorDopamine ReceptorEmotionalEncephalonEncephalon DiseasesEtiologyFiberGFA-ProteinGFAPGene ExpressionGenotypeGliaGlial CellsGlial Fibrillary Acid ProteinGlial Fibrillary Acidic ProteinGlial Intermediate Filament ProteinGoalsHistologicHistologicallyHomeostasisHortega cellHumanHydroxytyramineImmediate MemoryImmunofluorescenceImmunofluorescence ImmunologicImpaired cognitionImpairmentInjectionsIntracellular Communication and SignalingIntracranial CNS DisordersIntracranial Central Nervous System DisordersKolliker's reticulumLabelLinkLoxP-flanked alleleMaintenanceMajor TranquilizersMajor Tranquilizing AgentsMental disordersMental health disordersMetabolicMiceMice MammalsMicrogliaModelingModern ManMolecularMorphologic FindingMorphologyMurineMusNerve CellsNerve UnitNervous System DiseasesNervous System DisorderNeural CellNeurocyteNeurodevelopmental DisorderNeurogliaNeuroglial CellsNeuroimmuneNeuroleptic AgentsNeuroleptic DrugsNeurolepticsNeurologic DisordersNeurological Development DisorderNeurological DisordersNeuronsNon-neuronal cellNonneuronal cellPathologicPathway interactionsPhenotypePhysiologicPhysiologicalPhysiological HomeostasisPlayPopulationPrefrontal CortexProcessProliferatingPsychiatric DiseasePsychiatric DisorderReceptor SignalingRegulationReportingResearchRoleSchizophreniaSchizophrenic DisordersShort-Term MemorySignal TransductionSignal Transduction SystemsSignalingSortingSymptomsSynapsesSynapsinsSynapticTestingTissuesTransfectionUpregulationViralViral VectorVirusadulthoodastrocytic gliabehavior testbehavioral impairmentbehavioral testbiological signal transductionbrain controlcausationcell imagingcell sortingcell typecellular imagingchronic mental illnesscognitive dysfunctioncognitive functioncognitive lossdementia praecoxdendrite spinedisease causationexperimentexperimental researchexperimental studyexperimentsfloxedfloxed allelegitter cellglobal gene expressionglobal transcription profileimaging softwareimpaired behaviorimprovedindexingknock-downknockdownmental illnessmesogliametabolism measurementmetabolomemetabolomicsmetabonomemetabonomicsmicroglial cellmicrogliocytemorphological criteriamorphological signaturemouse modelmurine modelmutantnerve cementneuralneural inflammationneurodevelopmental diseaseneuroinflammationneuroinflammatoryneurological diseaseneuronalneuropsychiatric diseaseneuropsychiatric disordernovelpathwayperivascular glial cellpersistent mental illnesspharmacologicpsychiatric illnesspsychological disorderpsychoticreceptor expressionreceptor-mediated signalingscRNA sequencingscRNA-seqschizophrenicserious mental disorderserious mental illnesssevere mental disordersevere mental illnesssingle cell RNA-seqsingle cell RNAseqsingle cell expression profilingsingle cell transcriptomic profilingsingle-cell RNA sequencingsocial rolesynapsetranscriptometranscriptomicsvectorworking memory
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Full Description

Project Summary
Recent research in the study of brain functions is highlighting the important role of glial cells in

several human neurological and psychiatric disorders. The dopaminergic control of brain

functions is classically assigned to the effect of dopamine on neurons. However, D2R

expression has also been reported in astrocytes, questioning what their contribution in the

dopamine-dependent control of brain functions is.

Based on preliminary evidence showing an increase of astrocytes and microglia in the PFC of

mice with an altered control over dopamine synthesis and release, we hypothesize that D2R

signaling in astrocytes influences the activity of neighboring cells and induces microglia

proliferation. This mechanism could play a role in the control of PFC dependent behavior, gene

expression in astrocytes and microglia, as well as on the metabolites that they produce.

Thus, we propose to perform experiments to determine the impact of D2R signaling in astrocyte

on PFC functions. We will use viral vectors to knockdown D2R specifically in astrocytes in mice

with either a normal control of dopamine synthesis and release or in mutants where these

functions have been altered. This project is timely due to the increased involvement of glia in

brain disorders and promises to elucidate mechanisms previously unexplored.

Grant Number: 5R21MH136486-02
NIH Institute/Center: NIH

Principal Investigator: Emiliana Borrelli

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