Role of Lung MSC in Emphysema
Role of Lung MSC in Emphysema
批准号:
8704827
负责人:
SUSAN M MAJKA
金额:
$47.13万
依托单位:
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:
2013-08-01 至 2017-05-31
关键词:
ABCG2 geneAblationAddressAdultAffectAlveolarApoptosisArchitectureBlood VesselsBlood capillariesCartilageCell DeathCell LineCell ProliferationCell physiologyCellsChronic Obstructive Airway DiseaseColony-forming unitsCommunitiesDataDevelopmentDistalEndotheliumEngineeringEpithelialEpitheliumFatty acid glycerol estersFutureGasesGoalsHistologyHomeostasisHypoxiaIn VitroInvestigationKnock-outKnowledgeLigandsLungLung diseasesMaintenanceMeasuresMedicalMesenchymal Stem CellsModelingMusMyofibroblastNational Heart, Lung, and Blood InstitutePathologyPathway interactionsPatientsPhenotypePlayProcessProtocols documentationPulmonary EmphysemaReagentReporterResourcesRoleRosaSignal PathwaySignal TransductionSmall Interfering RNASmokingStem cellsStructureSuperoxide DismutaseSurfaceSystemTamoxifenTherapeutic InterventionTimeTissuesToxinUnited StatesVascular Diseasesalveolar epitheliumbasebonecapillarycell typeeffective therapyextracellularin vivoinhibitor/antagonistinnovationinsightinterestmembermortalitymouse modelnoveloxidant stresspromoterpublic health relevancepulmonary functionregenerativestemnesstherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The proposed studies will use innovative approaches to expand upon our knowledge of lung stem cells to broaden treatment paradigms for NHLBI-related lung diseases. We therefore hypothesize that the maintenance of lung MSC function by Wnt/¿-catenin signaling is necessary for pulmonary tissue homeostasis. We propose to examine lung MSC-dependent mechanisms of abnormal pulmonary architecture and function using novel mouse models both in vitro and in vivo. We will determine the mechanism by which adult lung MSCs contribute to pulmonary tissue architecture and function in vivo. In addition, we will determine the mechanism by which Wnt/¿-catenin signaling regulates lung MSCs function and affects tissue homeostasis using both in vitro and in vivo novel systems. These models will enable us to identify a cell type which may be suited as a therapeutic target. Additionally, these studies will generate important resources and reagents that will be of vast interest to both the scientific and medical communities.
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会议论文
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海外基金