Transcriptional control in the macrophage response to pathogens
Transcriptional control in the macrophage response to pathogens
批准号:
7640348
负责人:
ALAN A ADEREM
金额:
$82.84万
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:
2008-03-01 至 2009-02-28
关键词:
ActinsBinding SitesBioinformaticsBurkholderia pseudomalleiCase StudyCaspase-1CellsClassCluster AnalysisCommunicationCommunitiesComputer SimulationDataDatabasesElementsFlagellinFrancisella tularensisFundingGene DeletionGene ExpressionGene TargetingGenesGenomeGram-Negative BacteriaImmuneImmune responseImmune systemIn VitroInfectionInflammatoryInflammatory ResponseInterferon Type IKnowledgeLaboratoriesLeadListeria monocytogenesMacrophage ActivationMicroarray AnalysisMolecular ProfilingMusNull LymphocytesPathway interactionsPattern recognition receptorRNA InterferenceReceptor SignalingRegulator GenesResourcesRoleSalmonella typhimuriumSentinelSignal PathwaySignal TransductionSignaling MoleculeSystemSystems BiologyTechniquesTherapeuticToll-like receptorsTranscriptional RegulationVirulence FactorsWorkactivating transcription factorbasebiodefensechemokinecytokinedefined contributionin vivomacrophagemolecular recognitionmutantpathogenpolymerizationprogramspromoterquorum sensingresearch studyresponsetranscription factor
中文摘要
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英文摘要
Macrophages are key cells that direct innate immune responses to pathogens that are detected through
specific pattern recognition receptors. We will analyze the transcriptomes of macrophages infected with
Burkholderia pseudomallei and determine the transcription factors and signaling molecules that are activated
in response to infection. By examining macrophages deficient for central signaling molecules, we will
ascribe specific transcriptional clusters to TLR signaling (MyD88/Trif null cells), NLR signaling (Rip2 or
caspase 1 null cells) or type I interferon signaling (IFNaRI null cells). In parallel, we will determine the
transcriptional response to specific bacterial virulence factors or PAMPs in B. pseudomallei, including the
type III and VI secretion systems, actin polymerization, flagellin and quorum sensing. We will
computationally identify specific transcription factors that are activated and identify the compendium of genes
that each of three transcription factor regulates. Finally, we will validate the transcriptional networks that are
defined and determine their effect on B. pseudomallei infection in vivo and in vitro.
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海外基金