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<dc:title>Protein kinase C-η controls CTLA-4–mediated regulatory T cell function</dc:title>
<dc:creator>Kong, Kok-Fai</dc:creator>
<dc:creator>Fu, Guo</dc:creator>
<dc:creator>Zhang, Yaoyang</dc:creator>
<dc:creator>Yokosuka, Tadashi</dc:creator>
<dc:creator>Casas Requena, Javier</dc:creator>
<dc:creator>Canonigo-Balancio, Ann J</dc:creator>
<dc:creator>Becart, Stephane</dc:creator>
<dc:creator>Kim, Gisen</dc:creator>
<dc:creator>Yates, John R</dc:creator>
<dc:creator>Kronenberg, Mitchell</dc:creator>
<dc:creator>Saito, Takashi</dc:creator>
<dc:creator>Gascoigne, Nicholas R J</dc:creator>
<dc:creator>Altman, Amnon</dc:creator>
<dc:description>Producción Científica</dc:description>
<dc:description>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.</dc:description>
<dc:date>2024-01-08T14:33:26Z</dc:date>
<dc:date>2024-01-08T14:33:26Z</dc:date>
<dc:date>2014</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
<dc:identifier>Nature Immunology 15:465–472. https://doi.org/10.1038/ni.2866</dc:identifier>
<dc:identifier>1529-2908</dc:identifier>
<dc:identifier>https://uvadoc.uva.es/handle/10324/64301</dc:identifier>
<dc:identifier>10.1038/ni.2866</dc:identifier>
<dc:identifier>465</dc:identifier>
<dc:identifier>5</dc:identifier>
<dc:identifier>472</dc:identifier>
<dc:identifier>Nature Immunology</dc:identifier>
<dc:identifier>15</dc:identifier>
<dc:identifier>1529-2916</dc:identifier>
<dc:language>eng</dc:language>
<dc:rights>Atribución 4.0 Internacional</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
<dc:format>application/pdf</dc:format>
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