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pubmed-article:21110974pubmed:issue24lld:pubmed
pubmed-article:21110974pubmed:dateCreated2010-12-7lld:pubmed
pubmed-article:21110974pubmed:abstractTextTCR-microclusters (MC) are generated upon TCR stimulation prior to the immune synapse formation independently of lipid rafts. TCR-MCs contain receptors, kinases and adaptors, and function as the signaling unit for T cell activation. The TCR complex, but not the signaling molecules, is transported to the center to form cSMAC. The co-stimulation receptor CD28 joins the signaling region of cSMAC and recruits PKC? and Carma1. CTLA-4 accumulates in the same region and competes with CD28 for negative regulation of T cell activation. T cell activation is therefore mediated by two spatially distinct signaling compartments: TCR signaling by the peripheral TCR-MC and co-stimulation signal by the central signaling cSMAC.lld:pubmed
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pubmed-article:21110974pubmed:issn1873-3468lld:pubmed
pubmed-article:21110974pubmed:authorpubmed-author:SaitoTakashiTlld:pubmed
pubmed-article:21110974pubmed:authorpubmed-author:YokosukaTadas...lld:pubmed
pubmed-article:21110974pubmed:authorpubmed-author:Hashimoto-Tan...lld:pubmed
pubmed-article:21110974pubmed:copyrightInfoCopyright © 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.lld:pubmed
pubmed-article:21110974pubmed:issnTypeElectroniclld:pubmed
pubmed-article:21110974pubmed:day15lld:pubmed
pubmed-article:21110974pubmed:volume584lld:pubmed
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pubmed-article:21110974pubmed:pagination4865-71lld:pubmed
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pubmed-article:21110974pubmed:year2010lld:pubmed
pubmed-article:21110974pubmed:articleTitleDynamic regulation of T cell activation and co-stimulation through TCR-microclusters.lld:pubmed
pubmed-article:21110974pubmed:affiliationLaboratory for Cell Signaling, RIKEN Research Center for Allergy and Immunology, Tsurumi-ku, Yokohama, Japan. saito@rcai.riken.jplld:pubmed
pubmed-article:21110974pubmed:publicationTypeJournal Articlelld:pubmed
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