Coxiella burnetii Regulation of Macrophage cAMP/PKA Signaling
Coxiella burnetii Regulation of Macrophage cAMP/PKA Signaling
批准号:
8566257
负责人:
Daniel E Voth
金额:
$20.14万
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:
2013-05-10 至 2015-04-30
关键词:
ActinsAcute DiseaseAddressAerosolsAlveolar MacrophagesApoptosisApoptoticBiogenesisBiological AssayCell CommunicationCell DeathCell physiologyCellsChronicCoxiella burnetiiCyclic AMPCyclic AMP-Dependent Protein KinasesCytoskeletonDataDiseaseEndocarditisEnsureEventExploratory/Developmental GrantFluorescent ProbesGenerationsGoalsHumanImmuneImmune responseInfectionInhibition of ApoptosisIntegration Host FactorsLysosomesMaintenanceMembraneMonitorNatureParasitesPhagolysosomePhagosomesPhosphotransferasesPreventionProductionProtein KinaseProtein Kinase CProteinsQ FeverRegulationResearchRoleSecond Messenger SystemsSignal TransductionSmall Interfering RNAStagingStimulusTestingTherapeuticTranscriptional RegulationVacuoleVirulenceVirulentbasecombatdesignfluin vivoinsightmacrophageparasitismpathogenpolymerizationpreventprogramsprotein transportpublic health relevanceresearch studyresponsesecond messengertherapeutic targettrafficking
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Coxiella burnetii is the intracellular bacterial agent of human Q fever, a debilitating flu-like illness that can also present as severe chronic endocarditis. C. burnetii is spread by contaminated aerosols and targets alveolar macrophages in vivo, where the pathogen regulates vesicular trafficking to establish a phagolysosome-like parasitophorous vacuole (PV) in which to replicate. Eukaryotic kinase signaling is heavily involved in phagosome maturation and host responses to bacterial pathogens; however, their involvement in C. burnetii infection has not been fully defined. The current proposal is designed to test the hypothesis that C. burnetii manipulates host cAMP/PKA signaling to generate the PV and prevent host cell death. Aim 1 will elucidate the role of PKA in PV formation. The experiments in this aim will explore the requirement for PKA and actin-related protein trafficking to the PV. Aim 2 will determine the role of PKA in C. burnetii anti-apoptotic activity. These experiments will assess PKA-dependent inactivation of pro-apoptotic Bad and the requirement of this event for prevention of apoptosis. Aim 3 will probe the overall role of cAMP production in PV formation, bacterial replication, apoptosis inhibition, and transcriptional regulation. Collectively, the aims in the current proposal will explore a multi-functional role for cAMP/PKA signaling in C. burnetii parasitism of macrophages.
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