CD3 e functions in T cells
CD3 e functions in T cells
批准号:
7685132
负责人:
NICOLAI Stanislas Cyrille VAN OERS
金额:
$39.25万
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:
2008-09-20 至 2010-08-31
关键词:
ADRBK1 geneAddressBindingCD3 AntigensCell Surface ReceptorsCell membraneCell physiologyCellsComplexCytoplasmic TailG protein coupled receptor kinaseGRKITAMImmune responseInterventionLigandsMediatingModificationPeptidesPhospholipid InteractionPhospholipidsPhosphotransferasesProtein-Serine-Threonine KinasesProteinsReceptor Cross-TalkReceptor SignalingRoleSignal TransductionStretchingT-Cell DevelopmentT-Cell ReceptorT-LymphocyteViralchemokine receptorextracellularhuman CD3E proteininsightnovel therapeuticspathogenreceptorreceptor functionreceptor internalizationresponsetransmission process
中文摘要
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英文摘要
6. Project Summary
The T cell receptor is a multi-subunit receptor complex with four proteins involved in
intracellular signal transduction. Almost all studies to date have focused on a signaling
motif that is common to all four subunits. We provide preliminary evidence of second
signaling motif that is only present in one of the four chains, the CD3 epsilon chain. We
term this sequence the basic rich stretch, and have determined that it can interact with a
serine/threonine kinase termed GRK2, and can also interact with phospholipids.
We will delineate the functional role of this basic rich stretch by modifying it and
characterizing the effects of these modifications on 1) T cell receptor and chemokine
receptor cross-talk, 2) phospholipid interactions, and 3) T cell development and T cell
effector functions.
The findings from our studies will yield new mechanistic insights into T cell functions
during normal and abnormal immune responses. Novel therapeutic strategies for
intervening in T cell functions could emanate from our studies.
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