grant

Fluorescent Indicators for Imaging Synaptic Zinc in Cortical Sound Processing

Organization UNIVERSITY OF VIRGINIALocation CHARLOTTESVILLE, UNITED STATESPosted 30 Sept 2022Deadline 30 Jun 2027
NIHUS FederalResearch GrantFY20252-photonAD dementiaAddressAffinityAlzheimer Type DementiaAlzheimer disease dementiaAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's DiseaseAlzheimers DementiaAnimalsApoplexyAuditory CortexAuditory areaBindingBrainBrain Nervous SystemBrain Vascular AccidentCell BodyCell Communication and SignalingCell SignalingCellsCellular MembraneCerebral StrokeCerebrovascular ApoplexyCerebrovascular StrokeChelating AgentsChelatorsColorComplexonsCytosolDevelopmentDirected Molecular EvolutionEncephalonEngineeringEpilepsyEpileptic SeizuresEpilepticsFrequenciesGenerationsGenesHearing DisordersHearing problemImageImaging DeviceImaging InstrumentImaging ToolImaging technologyIn VitroIntracellular Communication and SignalingInvestigatorsIschemiaKO miceKnock-out MiceKnockout MiceLinkLocationMembraneMental DepressionMiceMice MammalsMolecular InteractionMurineMusNerve CellsNerve Impulse TransmissionNerve TransmissionNerve Transmitter SubstancesNerve UnitNervous System DiseasesNervous System DisorderNeural CellNeurobiologyNeurocyteNeurologic DisordersNeurological DisordersNeuromodulatorNeuronal TransmissionNeuronsNeurotransmittersNull MouseOrangesOrganellesOutcomePrimary Senile Degenerative DementiaProductivityPropertyProtein TraffickingProteinsResearch PersonnelResearchersRoleSLC30A3SLC30A3 geneSeizure DisorderSensoryShapesSignal TransductionSignal Transduction SystemsSignalingSolute Carrier Family 30 (Zinc Transporter), Member 3SpecificityStimulusStrokeSynapsesSynapticSynaptic VesiclesTestingTimeTransgenic MiceVariantVariationVesicleViral VectorZNT3ZincZinc Transporter 3Zn elementauditory diseaseauditory disorderauditory dysfunctionauditory problemauditory processingawakeaxon signalingaxon-glial signalingaxonal signalingbiological signal transductionbrain attackcell typecerebral vascular accidentcerebrovascular accidentdepressiondevelopmentaldirected evolutionepilepsiaepileptogenicextracellularfluorescence imagingfluorescent imagingglia signalingglial signalinghearing diseaseimagingimaging capabilitiesimprovedin vivoinformation processinginnovateinnovationinnovativeknockout genemembrane structurenerve signalingneural signalingneurobiologicalneurological diseaseneuronalneuronal signalingneurotransmissionnew technologynovelnovel technologiesperceptual stimulusphysicochemical phenomena related to the sensespresynapticprimary degenerative dementiaprotein transportpublic health relevanceresponsesenile dementia of the Alzheimer typesensory cortexsensory stimulussocial rolesoundsound frequencyspatial and temporalspatial temporalspatiotemporalstrokedstrokessynapsesynergismtraffickingtwo-photon
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Full Description

Abstract
Although the importance of synaptic Zn2+, as an emerging neuromodulator throughout the brain, has been widely

appreciated, the dynamics of synaptic Zn2+ release in response to naturally occurring stimuli remains largely

elusive. Genetically encoded Zn2+ indicators (GEZIs) derived from fluorescent proteins are popular tools for

imaging Zn2+ in the cytosol and intracellular organelles. However, fluorescence imaging of Zn2+ secretion in the

brain in live animals has not yet been achieved due to the limitations of current GEZIs (e.g., insufficient

extracellular membrane localization, mismatching affinity, and/or inadequate dynamic range and photostability).

This interdisciplinary multi-PI 4-year R01 project, led by Dr. Huiwang Ai with expertise in genetically encoded

indicators and fluorescence imaging and Dr. Thanos Tzounopoulos with expertise in studying the role of Zn2+ in

auditory processing, aims to (1) develop a new generation of GEZIs to address the hurdles for imaging secreted

Zn2+ in the brain in vivo, and (2) integrate the new GEZIs with our innovative ZnT3 cKO mice, which, for the first

time, allow for Cre-dependent expression of exogenous genes in ZnT3-expressing neurons and Dre-dependent

region- and cell type-specific conditional ZnT3 gene knockout, to identify the cell- and circuit-specificity of Zn2+

dynamics that shape cortical sound processing.

The project will lead to a novel capability of imaging synaptically released Zn2+ in the brain in awake behaving

animals. Our innovative strategy to optimize the exoplasmic location of GEZIs may be generalized to enhance

other genetically encoded indicators. Furthermore, because synaptic Zn2+ is a potent modulator throughout the

cortex, our findings on Zn2+ dynamics in the primary auditory cortex (A1) during sound processing will improve

the understanding of the roles of synaptic Zn2+ in cortical information processing beyond sensory cortices. We

expect our studies to catalyze an extensive array of studies on Zn2+-related neurobiology and neurological

diseases.

Grant Number: 5R01EB033172-04
NIH Institute/Center: NIH

Principal Investigator: Huiwang Ai

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