Interleukin 10 (IL-10)-mediated Immunosuppression: MARCH-I INDUCTION REGULATES ANTIGEN PRESENTATION BY MACROPHAGES BUT NOT DENDRITIC CELLS

J Biol Chem. 2015 Nov 6;290(45):27158-27167. doi: 10.1074/jbc.M115.682708. Epub 2015 Sep 25.

Abstract

Efficient immune responses require regulated antigen presentation to CD4 T cells. IL-10 inhibits the ability of dendritic cells (DCs) and macrophages to stimulate antigen-specific CD4 T cells; however, the mechanisms by which IL-10 suppresses antigen presentation remain poorly understood. We now report that IL-10 stimulates expression of the E3 ubiquitin ligase March-I in activated macrophages, thereby down-regulating MHC-II, CD86, and antigen presentation to CD4 T cells. By contrast, IL-10 does not stimulate March-I expression in DCs, does not suppress MHC-II or CD86 expression on either resting or activated DCs, and does not affect antigen presentation by activated DCs. IL-10 does, however, inhibit the process of DC activation itself, thereby reducing the efficiency of antigen presentation in a March-I-independent manner. Thus, IL-10 suppression of antigen presenting cell function in macrophages is March-I-dependent, whereas in DCs, suppression is March- I-independent.

Keywords: antigen presentation; dendritic cell; immunosuppression; interleukin; macrophage; major histocompatibility complex (MHC); ubiquitin ligase.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation*
  • B7-2 Antigen / metabolism
  • CD4-Positive T-Lymphocytes / immunology
  • Cell Differentiation / immunology
  • Dendritic Cells / cytology
  • Dendritic Cells / enzymology
  • Dendritic Cells / immunology
  • Down-Regulation
  • Enzyme Induction / immunology
  • Female
  • Histocompatibility Antigens Class II / metabolism
  • Immune Tolerance / physiology*
  • Interleukin-10 / immunology*
  • Lipopolysaccharides / immunology
  • Macrophages / enzymology*
  • Macrophages / immunology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Ovalbumin / immunology
  • Peptide Fragments / immunology
  • Ubiquitin-Protein Ligases / biosynthesis*
  • Ubiquitin-Protein Ligases / deficiency
  • Ubiquitin-Protein Ligases / genetics

Substances

  • B7-2 Antigen
  • Cd86 protein, mouse
  • Histocompatibility Antigens Class II
  • IL10 protein, mouse
  • Lipopolysaccharides
  • Peptide Fragments
  • ovalbumin (325-339)
  • Interleukin-10
  • Ovalbumin
  • MARCH1 protein, mouse
  • Ubiquitin-Protein Ligases