grant

Contribution of pulmonary ionocytes and neuroendocrine cells to ion transport-mediated airway surface liquid maintenance

Organization NATIONAL JEWISH HEALTHLocation DENVER, UNITED STATESPosted 25 Jul 2021Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY2025Active Ion TransportAffectAirway DiseaseAirway ResistanceAnimalsAsthmaBasal Transcription FactorBasal transcription factor genesBody TissuesBronchial AsthmaCF patientsCOPDCRE RecombinaseCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCas nuclease technologyCell BodyCell Communication and SignalingCell CountCell NumberCell SignalingCell to Cell Communication and SignalingCell-Cell SignalingCellsChronicChronic Obstruction Pulmonary DiseaseChronic Obstructive Lung DiseaseChronic Obstructive Pulmonary DiseaseCiliaClustered Regularly Interspaced Short Palindromic Repeats approachClustered Regularly Interspaced Short Palindromic Repeats methodClustered Regularly Interspaced Short Palindromic Repeats methodologyClustered Regularly Interspaced Short Palindromic Repeats techniqueClustered Regularly Interspaced Short Palindromic Repeats technologyCommunicationComplexCystic FibrosisDNA mutationDevelopmentDiseaseDisorderDysfunctionEnterobacteria phage P1 Cre recombinaseEpithelial CellsEpitheliumEquilibriumExonsFrequenciesFunctional disorderFutureGene AlterationGene MutationGeneral Transcription Factor GeneGeneral Transcription FactorsGenetic ChangeGenetic defectGenetic mutationHealthHereditaryHumanImmunofluorescenceImmunofluorescence ImmunologicImmunohistochemistryImmunohistochemistry Cell/TissueImmunohistochemistry Staining MethodImpairmentIndividualInheritedIntracellular Communication and SignalingIon ChannelIon TransportIonic ChannelsIonsIrritantsKnock-outKnockoutLiquid substanceLower respiratory tract structureLungLung ComplianceLung Respiratory SystemMaintenanceMeasuresMediatingMembraneMembrane ChannelsMethodsMiceMice MammalsModelingModern ManMorbidityMorbidity - disease rateMucociliary ClearanceMucociliary TransportMucous body substanceMucoviscidosisMucusMurineMusMutationNasalNasal EpitheliumNasal Passages NoseNeuroendocrine CellNosePassive Ion TransportPhysiopathologyPlayProcessPropertyPulmonary Body SystemPulmonary Organ SystemRegulationResearchRespiration DisordersRespiratory DisorderRespiratory EpitheliumRespiratory SystemRespiratory System, Nose, Nasal PassagesRespiratory TractsRespiratory tract structureRestRoleSeverity of illnessSignal TransductionSignal Transduction SystemsSignalingSiteStimulusStructureStructure of respiratory epitheliumSurfaceTechniquesTechnologyTimeTissuesTracheaTrachea ProperTracheal EpitheliumTranscriptTranscription Factor Proto-OncogeneTranscription factor genesUpper respiratory tractViscosityWater Movementsairway epitheliumairway surface liquidbacteriophage P1 recombinase Crebalancebalance functionbiological signal transductionbreathing disorderbronchial epitheliumcell typechronic obstructive pulmonary disordercommon treatmentcystic fibrosis patientsdefined contributiondevelopmentaldisease modeldisease severitydisorder modelfluidgene defectgenome mutationhuman modelimprovedindividuals with CFindividuals with cystic fibrosisinnovateinnovationinnovativeintercellular communicationliquidlower respiratory tractmembrane structuremodel of humanmortalitymouse modelmucousmurine modelmutant allelenovelparticlepathogenpathophysiologypatients with CFpatients with cystic fibrosispromoterpromotorpulmonaryrespiratory dysfunctionrespiratory tract epitheliumresponsescRNA sequencingscRNA-seqsingle cell RNA-seqsingle cell RNAseqsingle cell expression profilingsingle cell transcriptomic profilingsingle-cell RNA sequencingsocial roletargeted drug therapytargeted drug treatmentstargeted therapeutictargeted therapeutic agentstargeted therapytargeted treatmenttherapeutic agent developmenttherapeutic developmenttranscription factorupper airway tractwindpipe
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Full Description

PROJECT SUMMARY/ABSTRACT
Regulation of ion transport across the epithelium is vital to the health and function of the airways. Active

and passive ion and water movement is responsible for maintaining a periciliary fluid layer through which cilia

can move mucus and protect the airways against particles, irritants, and pathogens. While there is clear

evidence of disease caused by specific ion channel mutations (CFTR) as well acquired ion channel dysfunction

during/contributing to disease severity (COPD, asthma), the contribution of individual cell types of the

pulmonary epithelium to ion transport maintenance is poorly understood. Our experimental evidence

demonstrates that alterations in the frequencies of pulmonary ionocytes and neuroendocrine cells in airway

epithelial cultures result in dramatic differences in ion transport properties. Altogether, these cell types, along

with tuft-like cells, comprise about 0.8% of the total cell numbers in the human tracheal epithelium. Pulmonary

ionocytes are a newly identified cell type in the airways with extremely high expression of many ion channels

with vital functions in the respiratory tract. The dramatic impact of ionocytes and pulmonary neuroendocrine

cells on the ion transport properties of human airway cultures despite their rare frequencies led to our

hypothesis that these cell types are highly involved in the regulation and maintenance of ion transport balance

across the entire epithelium and are able to impact ion transport functions in other cell types through

intercellular communication. By utilizing novel murine models and applying innovative techniques to primary

murine and human airway epithelial cells, the research outlined in this proposal will define the contribution of

these rare cell types to the overall ion transport functions of the airway epithelium and will also define the role

of CFTR in these cells. We will thereby fully characterize the significance of pulmonary ionocytes and

neuroendocrine cells to ion transport-mediated airway surface liquid regulation and identify potential cell and

ion channel targets for therapeutic treatment of common airway diseases.

Grant Number: 5R01HL155325-05
NIH Institute/Center: NIH

Principal Investigator: Preston Bratcher

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