grant

Neurodegenerative reprograming of microglia in Alzheimer’s disease

Organization ADVANCED SCIENCE RESEARCH CENTERLocation NEW YORK, UNITED STATESPosted 15 Dec 2024Deadline 30 Nov 2029
NIHUS FederalResearch GrantFY20252-ketoglutarate2-oxoglutarateAD dementiaAD modelAD pathologyAPOE e4APOE-ε4APOEε4AddressAgingAllelesAllelomorphsAlzheimer Type DementiaAlzheimer disease dementiaAlzheimer risk factorAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's DiseaseAlzheimer's disease modelAlzheimer's disease pathologyAlzheimer's disease patientAlzheimer's disease riskAlzheimer's pathologyAlzheimer's patientAlzheimers DementiaAmyloidAmyloid SubstanceAmyloidosisAutomobile DrivingBehavior assessmentBiotechBiotechnologyBrainBrain Nervous SystemCausalityCell BodyCellsCellular StressCellular Stress ResponseChromatinCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalCollaborationsCore FacilityCreativenessDarknessDataDevelopmentDiseaseDisorderDisturbance in cognitionEIF-2 alphaEIF-2alphaEIF-2αElementsEncephalonEnzyme GeneEnzymesEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessEtiologyEventExposure toFutureGenesGeneticGenetic studyGrantHeterochromatinHeterogeneityHistonesHortega cellHumanImageImmuneImmunesImpaired cognitionIn VitroInitiation FactorsKnowledgeLate Onset Alzheimer DiseaseMT-bound tauMacrophageMass Photometry/Spectrum AnalysisMass SpectrometryMass SpectroscopyMass SpectrumMass Spectrum AnalysesMass Spectrum AnalysisMeasuresMetabolicMetabolic PathwayMiceMice MammalsMicrogliaMitochondriaModelingModern ManMolecularMorphologyMurineMusNerve DegenerationNeuron DegenerationNeurosciencesNew YorkOutcomePathologicPathologyPathway interactionsPeptide Initiation FactorsPhagocytesPhagocytic CellPhenotypePhosphorylationPlayPreventionPrimary Senile Degenerative DementiaProcessProductivityProtein PhosphorylationRegulationResearchResponse to stimulus physiologyRiskRisk FactorsRoleScienceSignal PathwayStimulusStressSynapsesSynapticTauopathiesTechniquesTestingTherapeuticTranslation Initiation FactorTranslational Initiation Factorabnormally aggregated tau proteinalpha Subunit Eukaryotic Initiation Factor 2alpha ketoglutaratealzheimer modelalzheimer riskamebocyteamyloid diseaseamyloid pathologyapo E-4apo E4apo epsilon4apoE epsilon 4apoE-4apoE4apolipoprotein E epsilon 4apolipoprotein E-4apolipoprotein E4behavioral assessmentbiological adaptation to stresscausationcell stresschromatin remodelingcofactorcognitive assessmentcognitive dysfunctioncognitive losscognitive testingcreativitydata integrationdemethylationdevelopmentaldisease causationdrivingeffective therapyeffective treatmentepigeneticallyfilamentous tau inclusiongitter cellhistone methylationimagingin vivoinnovateinnovationinnovativeinsightinsoluble aggregatelate onset alzheimerlife spanlifespanmesogliamicroglial cellmicrogliocytemicrotubule associated protein tau aggregationmicrotubule associated protein tau depositmicrotubule bound taumicrotubule-bound taumitochondrialmouse modelmultiomicsmultiple omicsmurine modelneural degenerationneurodegenerationneurodegenerativeneurological degenerationneuronal degenerationneuropathologic tauneuropathological tauneuroprotectionneuroprotectivenew drug treatmentsnew drugsnew pharmacological therapeuticnew therapeuticsnew therapynext generation therapeuticsnon-geneticnongeneticnovelnovel drug treatmentsnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel therapeuticsnovel therapypaired helical filament of taupanomicspathwaypatient living with Alzheimer's diseasepatient suffering from Alzheimer's diseasepatient with Alzheimer'spatient with Alzheimer's diseaseperivascular glial cellpreventpreventingprimary degenerative dementiaprogramsprotein aggregateprotein aggregationreaction; crisisself-aggregate tausenile dementia of the Alzheimer typesocial rolestimulus/responsestress responsestress; reactionsynapsetautau PHFtau Proteinstau accumulationtau aggregatetau aggregationtau associated neurodegenerationtau associated neurodegenerative processtau driven neurodegenerationtau factortau fibrillizationtau filamenttau induced degenerationtau induced neurodegenerationtau mediated neurodegenerationtau neurodegenerative diseasetau neurofibrillary tangletau neuropathologytau oligomertau paired helical filamenttau pathologytau pathophysiologytau polymerizationtau proteinopathytau related neurodegenerationtau-induced pathologytau-tau interactiontauopathic neurodegenerative disordertauopathytechnological innovationtherapeutic agent developmenttherapeutic developmenttoolα-ketoglutarateα-oxoglutarateαKGτ Proteinsτ aggregation
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ABSTRACT
Genetic studies implicate microglia—the brain's primary innate immune cells—as major determinants for the

risk of Alzheimer's Disease (AD). In murine AD models, microglia can assume phenotypes with protective or

neurodegenerative functions, such as driving aberrant synapse loss. This proposal aims to elucidate molecular

mechanisms that…

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Neurodegenerative reprograming of microglia in Alzheimer’s disease — ADVANCED SCIENCE RESEARCH CENTER | UNITED STATES | | Dev Procure