grant

Fluorescent Redox Indicators to Image Oxidative Stress in Alzheimer's Disease

Organization UNIVERSITY OF VIRGINIALocation CHARLOTTESVILLE, UNITED STATESPosted 1 May 2022Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY2026AD dementiaAD modelAD pathwayAD therapyAD treatmentAD-associated pathwaysAD-related pathwaysAD-specific pathwaysAccelerationActive OxygenAcuteAducanumabAlzheimer Type DementiaAlzheimer beta-ProteinAlzheimer disease dementiaAlzheimer disease mechanismAlzheimer disease treatmentAlzheimer pathwayAlzheimer sclerosisAlzheimer syndromeAlzheimer treatmentAlzheimer'sAlzheimer's Amyloid beta-ProteinAlzheimer's DiseaseAlzheimer's Disease PathwayAlzheimer's amyloidAlzheimer's disease modelAlzheimer's disease therapyAlzheimer's mechanismAlzheimer's related pathwaysAlzheimer's therapyAlzheimers DementiaAmyloid Alzheimer's Dementia Amyloid ProteinAmyloid Beta-PeptideAmyloid Protein A4Amyloid beta-ProteinAmyloid βAmyloid β-PeptideAmyloid β-ProteinAnimal Disease ModelsAnimal ModelAnimal Models and Related StudiesAnimalsAstrocytesAstrocytusAstrogliaBIIB037BindingBiochemicalBiologicalBleedingBody TissuesBrainBrain Nervous SystemBrain regionCausalityCell BodyCell Communication and SignalingCell Culture TechniquesCell SignalingCellsCephalicCerebral cortexCholesterolChronicCognition DisordersCognitiveComplementComplement ProteinsCranialCytosolDietary InterventionDirected Molecular EvolutionDisease ProgressionDoctor of MedicineDoctor of PhilosophyEncephalonEpilepsyEpileptic SeizuresEpilepticsEtiologyEvaluationEventExerciseFLIM imagingFluorescenceFrequenciesGenerationsGeneticGenetic EngineeringGenetic Engineering BiotechnologyGenetic Engineering Molecular BiologyGlutathioneH2O2HemorrhageHortega cellHuntington ChoreaHuntington DiseaseHuntington'sHuntington's DiseaseHuntingtons DiseaseHydrogen PeroxideHydroperoxideImageIntracellular Communication and SignalingInvestigationInvestigatorsJ20J20 mouseLocationM.D.MeasurementMediatingMetabolicMiceMice MammalsMicrogliaMitochondriaModelingMolecular InteractionMonoclonal Antibody TherapyMotionMurineMusNerve CellsNerve UnitNervous System DiseasesNervous System DisorderNeural CellNeurocyteNeurologic DisordersNeurological DisordersNeuronsNutrition InterventionsNutritional InterventionsOrganellesOutcomeOxidation-ReductionOxidative StressOxygen RadicalsParalysis AgitansParkinsonParkinson DiseasePathogenesisPh.D.PhDPhasePhotobleachingPhysiciansPlayPrimary ParkinsonismPrimary Senile Degenerative DementiaPro-OxidantsProcessProductionProductivityProteinsReactive Oxygen SpeciesRecombinant DNA TechnologyRedoxResearchResearch PersonnelResearchersRoleScientistSeizure DisorderSignal TransductionSignal Transduction SystemsSignalingSliceSpecificitySuperoxide AnionSuperoxide RadicalSuperoxidesSystemTRX geneTRX proteinTRX1TXN geneTestingThioredoxinTissue imagingTissuesUniversitiesValidationViral VectorVirginiaVisualizationa beta peptideabetaabeta accumulationabeta aggregationaduhelmage associated neurodegenerationage associated neurodegenerative diseaseage associated neurodegenerative disorderage dependent neurodegenerationage dependent neurodegenerative conditionage dependent neurodegenerative diseaseage dependent neurodegenerative disorderage related neurodegenerationage-driven neurodegenerative disordersage-related neurodegenerative diseaseage-related neurodegenerative disorderaging associated neurodegenerationaging associated neurodegenerative diseaseaging related neurodegenerationaging related neurodegenerative diseaseaging related neurodegenerative disorderalzheimer modelamyloid betaamyloid beta accumulationamyloid beta aggregationamyloid β accumulationamyloid β aggregationamyloid-b proteinastrocytic gliaaβ accumulationaβ aggregationbeta amyloid fibrilbiologicbiological signal transductionblood lossbrain tissuecausationcell culturecell culturescell typecofactorcognitive diseasecognitive disordercognitive syndromecomplementationdevelop therapydiet interventiondirected evolutiondisease causationepilepsiaepileptogenicfluorescence imagingfluorescence life-time imagingfluorescence life-time imaging microscopyfluorescence lifetime imagingfluorescence lifetime imaging microscopyfluorescent imaginggamma-L-Glu-L-Cys-Glygamma-L-Glutamyl-L-Cysteinylglycinegenetically engineeredgitter cellglobal healthimage-based methodimagingimaging capabilitiesimaging methodimaging modalityimaging systemin vivoinnovateinnovationinnovativeintervention developmentmAB-based therapymAb therapymAb-based therapeuticsmechanisms in ADmechanisms in Alzheimer's diseasemesogliamicroglial cellmicrogliocytemitochondrialmodel of animalmouse modelmultiplexed imagingmurine modelnerve cell deathnerve cell lossneurological diseaseneuron cell deathneuron cell lossneuron deathneuron lossneuron toxicityneuronalneuronal cell deathneuronal cell lossneuronal deathneuronal lossneuronal toxicityneurotoxicityoxidation reduction reactionpathways associated with ADpathways associated with Alzheimer'spathways contribute to Alzheimer'spathways involved in Alzheimer diseasepathways that contribute to ADpathways that drive ADpathways underlying Alzheimer'sperivascular glial cellprimary degenerative dementiapublic health relevancequantitative imagingratiometricresponseresponse to therapyresponse to treatmentsenile dementia of the Alzheimer typesocialsocial rolesoluble amyloid precursor proteinsynergismtech developmenttechnology developmenttechnology implementationtechnology validationtherapeutic responsetherapy developmenttherapy responsetooltreatment developmenttreatment responsetreatment responsivenessvalidations
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Full Description

Abstract
Alzheimer's disease (AD) and other age-related neurodegenerative disorders have become a global health and

social challenge. Although the exact cause of AD is still under investigation, among various AD hypotheses,

oxidative stress is considered either a causative factor or a critical cofactor in cascades of events leading to neuron

death. Because of the importance of oxidative stress in the etiology and pathogenesis of AD, research tools that

can conveniently evaluate oxidative stress in AD models are expected to greatly catalyze and accelerate research

on AD.

The overall objective of this R01 project is to develop and optimize genetically encoded fluorescent redox

indicators (GERIs) for the convenient evaluation of oxidative stress in AD mouse models. This project uses the

synergy of two productive investigators at the University of Virginia (UVA). Huiwang Ai (Ph.D., PI) has expertise

in genetically encoded fluorescent indicators and fluorescence imaging of redox signaling in live cells and animals.

Heather Ferris (M.D./Ph.D., Co-I) is a physician-scientist with a research focus on metabolic drivers in AD and

other cognitive disorders. Leveraging our complementary expertise and strong preliminary results, we will

develop and optimize GERIs for intensity-based ratiometric (Aim 1) and lifetime (Aim 2) imaging. We

hypothesize that the GERIs can be used to conveniently assess oxidative stress status in AD mouse models during

disease progression and in response to therapies, and we will test this hypothesis in Aim 3.

The proposed research will lead to a toolbox of GERIs for quantitative imaging of oxidative stress in

animal models. These innovative tools will allow precise measurement of specific redox parameters in specific

cell types and subcellular domains, facilitating our understanding of AD mechanisms and further intervention

development. Although the focus of the current phase of this project is on technology development and validation,

we expect our study will catalyze an extensive array of biological studies on ROS and oxidative stress in the brain,

resulting in a tremendous amplification of the impact of this project.

Grant Number: 5R01AG077773-03
NIH Institute/Center: NIH

Principal Investigator: Huiwang Ai

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