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dc.contributor.authorKong, Kok-Fai
dc.contributor.authorFu, Guo
dc.contributor.authorZhang, Yaoyang
dc.contributor.authorYokosuka, Tadashi
dc.contributor.authorCasas, Javier
dc.contributor.authorCanonigo-Balancio, Ann J
dc.contributor.authorBecart, Stephane
dc.contributor.authorKim, Gisen
dc.contributor.authorYates, John R
dc.contributor.authorKronenberg, Mitchell
dc.contributor.authorSaito, Takashi
dc.contributor.authorGascoigne, Nicholas R J
dc.contributor.authorAltman, Amnon
dc.date.accessioned2024-01-08T14:33:26Z
dc.date.available2024-01-08T14:33:26Z
dc.date.issued2014
dc.identifier.citationNature Immunology 15:465–472. https://doi.org/10.1038/ni.2866es
dc.identifier.issn1529-2908es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/64301
dc.descriptionProducción Científicaes
dc.description.abstractRegulatory T (Treg) cells, which maintain immune homeostasis and self-tolerance, form an immunological synapse (IS) with antigen-presenting cells (APCs). However, signaling events at the Treg cell IS remain unknown. Here we show that the kinase PKC-η associated with CTLA-4 and was recruited to the Treg cell IS. PKC-η-deficient Treg cells displayed defective suppressive activity, including suppression of tumor immunity but not of autoimmune colitis. Phosphoproteomic and biochemical analysis revealed an association between CTLA-4-PKC-η and the GIT2-αPIX-PAK complex, an IS-localized focal adhesion complex. Defective activation of this complex in PKC-η-deficient Treg cells was associated with reduced depletion of CD86 from APCs by Treg cells. These results reveal a CTLA-4-PKC-η signaling axis required for contact-dependent suppression and implicate this pathway as a potential cancer immunotherapy target.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleProtein kinase C-η controls CTLA-4–mediated regulatory T cell functiones
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1038/ni.2866es
dc.identifier.publicationfirstpage465es
dc.identifier.publicationissue5es
dc.identifier.publicationlastpage472es
dc.identifier.publicationtitleNature Immunologyes
dc.identifier.publicationvolume15es
dc.peerreviewedSIes
dc.identifier.essn1529-2916es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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