Membrane-type 1 Matrix Metalloproteinase in COPD
Membrane-type 1 Matrix Metalloproteinase in COPD
批准号:
7531173
负责人:
JEFFREY J ATKINSON
金额:
$12.38万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-11 至 2013-06-30
关键词:
AcuteAddressAdultAdvisory CommitteesAffectAgeAge-MonthsAlveolarAlveolar MacrophagesAlveolar wallAnimalsApplications GrantsAreaArthritisBasement membraneBindingBiological MarkersBirthBlood - brain barrier anatomyBody WeightBone GrowthBone Marrow TransplantationCD44 AntigensCD44 geneCause of DeathCell Adhesion MoleculesCell Surface ProteinsCell membraneCell surfaceCellsCellular biologyChondrocytesChronicChronic Obstructive Airway DiseaseCigarette smoke-induced emphysemaClara cellCleaved cellClinicalCollagenComplexDefectDevelopmentDiseaseDrosophila pros proteinDuct (organ) structureElastasesEndopeptidasesEndothelial CellsEnvironmentEpithelialEpithelial CellsEpitheliumExtracellular MatrixFailureFamilyFibrillar CollagenFibroblastsFutureGelGelatinase AGrowthHemopexinHumanIn VitroIndividualInflammationInflammatoryInjuryIntegrinsInterstitial CollagenaseKnowledgeKyphosis deformity of spineLaboratoriesLamininLengthLigandsLocalizedLungLung InflammationLung diseasesMalignant NeoplasmsMatrix MetalloproteinasesMediatingMembrane ProteinsMethodsModificationMolecular Biology TechniquesMolecular and Cellular BiologyMorphogenesisMultiple SclerosisMusNaphthaleneNaphthalenesNeoplasm MetastasisPancreatic ElastasePathogenesisPathologicPatientsPeptide HydrolasesPeripheralPhysiciansPhysiologicalPlayPrincipal InvestigatorProductionProtein C InhibitorProtein OverexpressionProteinsPulmonary EmphysemaRecyclingResearchResearch PersonnelRodentRoleScientistSiteSkeletal systemSmokeSurfaceTechnologyTemperatureTissue Inhibitor of Metalloproteinase-1TissuesTransgenic MiceTransgenic OrganismsTransglutaminasesUniversitiesUp-RegulationWashingtonWeekWorkairway remodelingalveolar type II cellbasecancer cellcareercell motilitycigarette smoke-inducedcigarette smokingcoated pitcollagenaseenzyme activityhuman MMP14 proteinin vivoinjury and repairinterestinterstitiallong bonelung developmentlung injurymacrophagemembrane-type matrix metalloproteinasemigrationmonocytemouse modelnovelperipheral bloodpostnatalprogramsrole modelsizeskillswasting
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Chronic obstructive pulmonary disease (COPD) is a disease of major proportion and a critical target for future research. The development of new investigators with expertise in ths field will be an essential step in progress towards our understanding of the pathogenesis and treatment of COPD. This grant proposal requests support for the transition in my career from a clinical scientist with knowledge in molecular and cellular biology of lung disorders into an independent investigator with a focus in utilizing molecular biology techniques in protease-mediated lung disorders, such as COPD. For the past several decades, the development of COPD has been attributed to cigarette smoke induced-inflammation and elastase production, but recently collagenases have been implicated in the development of emphysema. I have found that membrane-type 1 matrix metalloproteinase (MT1-MMP), a collagenase, is expressed by alveolar macrophages and airway epithelial cells in a mouse model of cigarette smoke exposure induced-COPD and in the airway after naphthalene-induced acute airway epithelial injury, suggesting it plays a role in lung injury and repair. Based on these observations, I hypothesize that MT1-MMP is involved in the pathogenesis of COPD. I will examine alveolar wall destruction, airway remodeling, macrophage migration and inflammation in the presence and absence of MT1-MMP to determine the role and consequences of MT1-MMP production that occurs during cigarette smoke exposure. The work proposed in this application will be performed at Washington University in the laboratory of Dr. Robert Senior in conjunction with an Advisory Committee composed of experts in the fields of transgenic mouse technologies, epithelial cell biology and extracellular matrix. This is an environment that has proven successful in the development of physician scientists for research careers. In addition to uncovering a novel target in the treatment of COPD, this proposal will provide career development, so that I will attain skills to do COPD research independently.
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会议论文
MOLECULAR MECHANISMS OF CHRONIC AIRWAY AND ALVEOLAR DISEASE IN HIV
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批准号:8637535
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项目类别:
-
资助金额:$59.87万
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财政年份:2013
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负责人:JEFFREY J ATKINSON
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依托单位:
MOLECULAR MECHANISMS OF CHRONIC AIRWAY AND ALVEOLAR DISEASE IN HIV
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批准号:8743253
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项目类别:
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资助金额:$63.61万
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财政年份:2013
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负责人:JEFFREY J ATKINSON
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依托单位:
Membrane-type 1 Matrix Metalloproteinase in COPD
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批准号:8286947
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项目类别:
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资助金额:$12.42万
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财政年份:2008
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负责人:JEFFREY J ATKINSON
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依托单位:
Membrane-type 1 Matrix Metalloproteinase in COPD
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批准号:8094286
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项目类别:
-
资助金额:$12.42万
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财政年份:2008
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负责人:JEFFREY J ATKINSON
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依托单位:
Membrane-type 1 Matrix Metalloproteinase in COPD
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批准号:7880083
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项目类别:
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资助金额:$12.41万
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财政年份:2008
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负责人:JEFFREY J ATKINSON
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依托单位:
Membrane-type 1 Matrix Metalloproteinase in COPD
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批准号:7656595
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项目类别:
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资助金额:$12.39万
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财政年份:2008
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负责人:JEFFREY J ATKINSON
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依托单位:
海外基金