The DC-HIL/syndecan-4 pathway regulates autoimmune responses through myeloid-derived suppressor cells

J Immunol. 2014 Mar 15;192(6):2576-84. doi: 10.4049/jimmunol.1301857. Epub 2014 Feb 10.

Abstract

Having discovered that the dendritic cell (DC)-associated heparan sulfate proteoglycan-dependent integrin ligand (DC-HIL) receptor on APCs inhibits T cell activation by binding to syndecan-4 (SD-4) on T cells, we hypothesized that the DC-HIL/SD-4 pathway may regulate autoimmune responses. Using experimental autoimmune encephalomyelitis (EAE) as a disease model, we noted an increase in SD-4(+) T cells in lymphoid organs of wild-type (WT) mice immunized for EAE. The autoimmune disease was also more severely induced (clinically, histologically, and immunophenotypically) in mice knocked out for SD-4 compared with WT cohorts. Moreover, infusion of SD-4(-/-) naive T cells during EAE induction into Rag2(-/-) mice also led to increased severity of EAE in these animals. Similar to SD-4 on T cells, DC-HIL expression was upregulated on myeloid cells during EAE induction, with CD11b(+)Gr-1(+) myeloid-derived suppressor cells (MDSCs) as the most expanded population and most potent T cell suppressor among the myeloid cells examined. The critical role of DC-HIL was supported by DC-HIL gene deletion or anti-DC-HIL treatment, which abrogated T cell suppressor activity of MDSCs, and also by DC-HIL activation inducing MDSC expression of IFN-γ, NO, and reactive oxygen species. Akin to SD-4(-/-) mice, DC-HIL(-/-) mice manifested exacerbated EAE. Adoptive transfer of MDSCs from EAE-affected WT mice into DC-HIL(-/-) mice reduced EAE severity to the level of EAE-immunized WT mice, an outcome that was precluded by depleting DC-HIL(+) cells from the infused MDSC preparation. Our findings indicate that the DC-HIL/SD-4 pathway regulates autoimmune responses by mediating the T cell suppressor function of MDSCs.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adoptive Transfer
  • Animals
  • Autoimmunity / genetics
  • Autoimmunity / immunology*
  • CD11b Antigen / immunology
  • CD11b Antigen / metabolism
  • Cells, Cultured
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology
  • DNA-Binding Proteins / metabolism
  • Encephalomyelitis, Autoimmune, Experimental / genetics
  • Encephalomyelitis, Autoimmune, Experimental / immunology
  • Encephalomyelitis, Autoimmune, Experimental / metabolism
  • Eye Proteins / genetics
  • Eye Proteins / immunology*
  • Eye Proteins / metabolism
  • Female
  • Flow Cytometry
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology*
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Cells / immunology*
  • Myeloid Cells / metabolism
  • Myeloid Cells / transplantation
  • Nitric Oxide / immunology
  • Nitric Oxide / metabolism
  • Reactive Oxygen Species / immunology
  • Reactive Oxygen Species / metabolism
  • Receptors, Chemokine / immunology
  • Receptors, Chemokine / metabolism
  • Spleen / immunology
  • Spleen / metabolism
  • Spleen / pathology
  • Syndecan-4 / genetics
  • Syndecan-4 / immunology*
  • Syndecan-4 / metabolism
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism

Substances

  • CD11b Antigen
  • DNA-Binding Proteins
  • Eye Proteins
  • Gpnmb protein, mouse
  • Gr-1 protein, mouse
  • Membrane Glycoproteins
  • Rag2 protein, mouse
  • Reactive Oxygen Species
  • Receptors, Chemokine
  • Syndecan-4
  • Nitric Oxide
  • Interferon-gamma