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    • PRODUZIONE SCIENTIFICA
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    • Dpto. Bioquímica y Biología Molecular y Fisiología
    • DEP06 - Artículos de revista
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    Por favor, use este identificador para citar o enlazar este ítem:https://uvadoc.uva.es/handle/10324/64301

    Título
    Protein kinase C-η controls CTLA-4–mediated regulatory T cell function
    Autor
    Kong, Kok-Fai
    Fu, Guo
    Zhang, Yaoyang
    Yokosuka, Tadashi
    Casas Requena, JavierAutoridad UVA Orcid
    Canonigo-Balancio, Ann J
    Becart, Stephane
    Kim, Gisen
    Yates, John R
    Kronenberg, Mitchell
    Saito, Takashi
    Gascoigne, Nicholas R J
    Altman, Amnon
    Año del Documento
    2014
    Descripción
    Producción Científica
    Documento Fuente
    Nature Immunology 15:465–472. https://doi.org/10.1038/ni.2866
    Abstract
    Regulatory 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.
    ISSN
    1529-2908
    Revisión por pares
    SI
    DOI
    10.1038/ni.2866
    Idioma
    eng
    URI
    https://uvadoc.uva.es/handle/10324/64301
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    openAccess
    Aparece en las colecciones
    • DEP06 - Artículos de revista [352]
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