Chromosome 17q, allergic inflammation, and remodeling
Chromosome 17q, allergic inflammation, and remodeling
批准号:
8661705
负责人:
DAVID H BROIDE
金额:
$38.75万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-05-15 至 2018-04-30
关键词:
17q17q21ADAM-8AllergensAllergic inflammationAntibodiesAsthmaCXC ChemokinesCa(2+)-Transporting ATPaseCellsChromosomesDataDevelopmentEarly DiagnosisEarly InterventionEarly identificationEndoplasmic ReticulumEpithelialEpithelial CellsEpitheliumFutureGelatinase BGenesHumanIL8 geneIgEIn VitroInflammationInflammatoryInterferonsInvestigationLabelLengthLigaseLinkLungLung diseasesMediatingMetalloproteasesModelingMucous body substanceMusMutant Strains MiceNatureOrosomucoidOutcomePathogenesisPathway interactionsPhysiologicalPlayPopulation HeterogeneityProteinsPubMedPublicationsPublishingReagentResearch PersonnelRhinovirusRoleScienceSignal Transduction PathwayTestingTransfectionTransgenic MiceTransgenic OrganismsViralVirusactivating transcription factorairway epitheliumairway inflammationairway remodelingbasebeta-Chemokineschemokinecytokineendonucleaseeosinophilic inflammationgenetic associationgenome wide association studyhigh riskin vivoinsightknock-downmRNA Transcript Degradationmouse modelnoveloligoadenylatepreventpublic health relevancerepairedrespiratory virusresponsetransgene expression
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Genome wide association studies have identified strong linkage between chromosome 17q21 and asthma. The focus of this proposal is on ORMDL-3, a protein localized to chromosome 17q21, which has been highly linked to asthma in several genome wide association studies. The investigation of the function of ORMDL-3 in the lung in asthma in this proposal will be enhanced by the development of unique reagents in the investigators lab (e.g. universal and cell specific ORMDL-3 transgenic and ORMDL-3 deficient mice; development of antibody to ORMDL to perform immunohistological). Based on our preliminary data we hypothesize that allergen induced ORMDL-3 expression regulates expression of multiple epithelial pathways (inflammation, remodeling, repair), as well as the ER ATF6 pathway which together play an important role in the pathogenesis of asthma. The studies proposed will use in vitro (knock down or over-expression of ORMDL-3 in lung cells) and in vivo studies (ORMDL-3 transgenic and ORMDL-3 deficient mice) to determine the role of ORMDL3 in the pathogenesis of allergen and rhinoviral induced asthma.
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国内基金
海外基金
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依托单位: