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HDAC11 is a regulator of diverse immune functions
Authors:Cansu Yanginlar  Colin Logie
Affiliation:Department of Molecular Biology, Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands
Abstract:Histone deacetylases deacetylate histone and non-histone protein targets. Aberrant HDAC expression and function have been observed in several diseases, which make these enzymes attractive treatment targets. Here, we summarize recent literature that addresses the roles of HDAC11 on the regulation of different immune cells including neutrophils, myeloid derived suppressor cells and T-cells. HDAC11 was initially identified as a negative regulator of the well-known anti-inflammatory cytokine IL-10. Hence, antagonizing HDAC11 activity may have anti-tumor potential, whereas activating HDAC11 may be useful to treat chronic inflammation or autoimmunity. However, to anticipate biological side-effects of HDAC11 modulators, more molecular insights will be required.
Keywords:APC  antigen presenting cell  CTCL  cutaneous T-cell lymphoma  DAMP  Damage associated molecular pattern  DC  dendritic cell  FDA  U.S. Food and Drug Administration  GVHD  graft versus host disease  HAT  histone acetyltransferase  HDAC  histone deacetylase  HDACi  Histone deacetylase inhibitor  HEK293  Human embryonic kidney cells 293  IFN  interferon  IL  interleukin  miR145  microRNA 145  MDSC  myeloid derived suppressor cell  GO  gene ontology  PAMP  Pathogen associated molecular pattern  PTCL  peripheral T-cell lymphoma  SAHA  suberoylanilide hydroxamic acid  siRNA  Small interfering RNA  TcR  T cell receptor  Treg  regulatory T cell  TNF-ɑ  Tumor necrosis factor ɑ  UTR  Untranslated region  HDAC11  Epigenetics  Immune system  HDACi
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