14
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Divergent roles of histone deacetylase 6 (HDAC6) and histone deacetylase 11 (HDAC11) on the transcriptional regulation of IL10 in antigen presenting cells.

      Molecular Immunology
      Animals, Antigen-Presenting Cells, immunology, Cell Line, Gene Expression Regulation, Histone Deacetylases, genetics, Immune Tolerance, Interleukin-10, Lymphocyte Activation, Macrophages, Male, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Mice, Knockout, Promoter Regions, Genetic, RNA Interference, RNA, Small Interfering, T-Lymphocytes, Transcription, Genetic, Transcriptional Activation

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The anti-inflammatory cytokine IL-10 is a key modulator of immune responses. A better understanding of the regulation of this cytokine offers the possibility of tipping the balance of the immune response toward either tolerance, or enhanced immune responses. Histone deacetylases (HDACs) have been widely described as negative regulators of transcriptional regulation, and in this context, the primarily nuclear protein HDAC11 was shown to repress il-10 gene transcriptional activity in antigen-presenting cells (APCs). Here we report that another HDAC, HDAC6, primarily a cytoplasmic protein, associates with HDAC11 and modulates the expression of IL-10 as a transcriptional activator. To our knowledge, this is the first demonstration of two different HDACs being recruited to the same gene promoter to dictate divergent transcriptional responses. This dynamic interaction results in dynamic changes in the expression of IL-10 and might help to explain the intrinsic plasticity of the APC to determine T-cell activation versus T-cell tolerance. Copyright © 2014 Elsevier Ltd. All rights reserved.

          Related collections

          Author and article information

          Comments

          Comment on this article