| Literature DB >> 26869226 |
Noa Beatriz Martín-Cófreces1,2, Francisco Sánchez-Madrid1,2, Norman Núñez-Andrade1,2, Salvador Iborra3, Antonio Trullo4,5, Olga Moreno-Gonzalo1,2, Enrique Calvo6, Elena Catalán7, Gaël Menasche8, David Sancho3, Jesús Vázquez6, Tso-Pang Yao9.
Abstract
HDAC6 is a tubulin deacetylase involved in many cellular functions related to cytoskeleton dynamics, including cell migration and autophagy. In addition, HDAC6 affects antigen-dependent CD4(+)T cell activation. In this study, we show that HDAC6 contributes to the cytotoxic function of CD8(+)T cells. Immunization studies revealed defective cytotoxic activity in vivo in the absence of HDAC6. Adoptive transfer of wild-type or Hdac6(-/-)CD8(+)T cells to Rag1(-/-)mice demonstrated specific impairment in CD8(+)T cell responses against vaccinia infection. Mechanistically, HDAC6-deficient cytotoxic T lymphocytes (CTLs) showed defective in vitro cytolytic activity related to altered dynamics of lytic granules, inhibited kinesin-1-dynactin-mediated terminal transport of lytic granules to the immune synapse and deficient exocytosis, but not to target cell recognition, T cell receptor (TCR) activation or interferon (IFN)γ production. Our results establish HDAC6 as an effector of the immune cytotoxic response that acts by affecting the dynamics, transport and secretion of lytic granules by CTLs.Entities:
Keywords: Histone deacetylase 6; Kinesin 1; Lytic granule
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Year: 2016 PMID: 26869226 PMCID: PMC5023047 DOI: 10.1242/jcs.180885
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285