Role of Surfactant in Mycoplasma Pulmonary Infection and Exacerbation
Role of Surfactant in Mycoplasma Pulmonary Infection and Exacerbation
批准号:
7407098
负责人:
Julie Gunnells Ledford
金额:
$4.68万
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:
2008-01-01 至 2010-12-31
关键词:
A MouseAccountingAcuteAffinityAllergensAllergicAlveolar MacrophagesAntigensAsthmaAttenuatedBacteriaBindingBiological AssayBone MarrowBronchoalveolar LavageBronchoalveolar Lavage FluidCell MaturationCell physiologyCell surfaceChronicChronic Obstructive Airway DiseaseCommunitiesConditioned Culture MediaConfocal MicroscopyDendritic CellsDevelopmentDiseaseEnvironmental Risk FactorEpithelialExtrinsic asthmaFlow CytometryGeneral PopulationGentamicinsGrowthHost DefenseHumanHyperactive behaviorImmune systemImmunityIn VitroInfectionInflammationInflammatoryInvestigationKnockout MiceLinkLipopolysaccharidesLungLung diseasesMeasuresMediatingMediator of activation proteinMicrobeModelingMusMycoplasmaMycoplasma pneumoniaeNatural ImmunityNatural Killer CellsNot DefinedOpsoninOvalbuminPathogenicityPatientsPhagocytosisPlayPneumoniaProductionProteinsPulmonary Surfactant-Associated Protein ARangeResearchResearch DesignResistanceRoleSymptomsTestingVirusatypical pneumoniacytokinein vivomacrophagemicrobialneutrophilpathogenresearch studyresponsesurfactantuptake
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Hypothesis: The overall hypothesis to be tested in this proposal is that SP-A plays an important protective role in pulmonary host defense against M. pneumoniae (MP) infections and airway reactivity by modulating the transition from innate to adaptive immunity. Specific Aims: (1) to investigate the role of SP-A in regulating DC maturation and cytokine modulation in response to M. pneumoniae infection in vitro; (2) to determine if SP-A acts as an opsonin and aids in the uptake of M. pneumoniae by immature DCs and alveolar macrophages, thereby increasing clearance while decreasing epithelial binding and insult to the host; (3) to examine the effects of SP-A on M. pneumoniae induced airway hyperactivity using mice deficient in SP-A to better understand the role of SP-A in an experimental asthma setting. Study Design: The role of SP-A in regulating MP-induced DC maturation and cytokine modulation will first be examined by studying bone marrow derived dendritic cells cultured from wild type and SP-A null mice. These parameters will then be assessed using mice deficient in SP-A infected with M. pneumoniae. I will perform more comprehensive experiments examining MP clearance, uptake and epithelial damage and determine if SP-A mediates these activities. Experiments using SP-A null mice with experimental allergic asthma will be used to study the role of SP-A in MP induced asthma exacerbations. Relevance: The relationship between allergen, infection and asthma comprises a spectrum ranging from exacerbation of established disease to development and persistence of disease. The interactions between the innate and adaptive immune systems may be pivotal in ultimately determining the phenotypic presentation of asthma. Surfactant proteins have not been widely studied in asthma but are known to play important roles in host defense and modulation of inflammation which may contribute to the development and persistence of asthma. The research proposed in this project will aid in elucidating the role of Surfactant Protein-A in M. pneumoniae pulmonary infections specifically associated with asthma related symptoms.
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依托单位:
海外基金