PKC-theta function in RORgammat-regulated Th17 differentiation
PKC-theta function in RORgammat-regulated Th17 differentiation
批准号:
8580188
负责人:
Zuoming Sun
金额:
$41.5万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-06-01 至 2015-10-31
关键词:
AgreementAnimal ModelAutoimmune DiseasesAutoimmunityCell physiologyCellsCellular biologyCollaborationsDataDevelopmentDrug TargetingEquilibriumExperimental Autoimmune EncephalomyelitisGenerationsGoalsImmune responseImmune systemImmunityIn VitroInflammatoryKnowledgeLearningMediatingModelingMolecularMultiple SclerosisNuclear Orphan ReceptorPharmacologic SubstancePhosphorylationPreventionProtein Kinase CReceptor ActivationReceptor SignalingRecruitment ActivityRegulationRegulatory T-LymphocyteResearchRetinoidsRoleSteroid ReceptorsT-Cell ReceptorT-LymphocyteTestingTherapeuticTherapeutic UsesTimeWorkabstractingarmbaseclinical applicationin vivoinhibitor/antagonistinnovationmouse modelnovelpathogenpreventpublic health relevance
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Abstract Generation of robust Th17 immune responses required for clearance of certain pathogens depends on promoting Th17 while reciprocally inhibiting Treg formation. Whereas, effective prevention of Th17-mediated autoimmunity such as EAE depends on inhibiting pathogenic Th17 while reciprocally promoting Treg formation. However, little is known about the mechanisms responsible for coordination of Th17 and Treg differentiation. Our preliminary results demonstrated that PKC-theta is a critical checkpoint for reciprocal Th17 and Treg differentiation. The proposed studies will investigate the function of PKC- theta and RORyt in the reciprocal Th17 and iTreg differentiation. Based on the knowledge learned from the studies, we expect to develop PKC-8-based treatments for prevention of EAE, an animal model of multiple sclerosis. It is expected that such treatments will have a broader applicability in the prevention of Th17-mediated autoimmunity. In addition, the proposed research has significance to basic T cell biology, as it is expected to reveal novel molecular mechanisms for PKC- theta -mediated TCR signals in the coordination of Th17 and iTreg differentiation.
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