V-set and Ig domain-containing 4 (VSIG4)-expressing hepatic F4/80+ cells regulate oral antigen-specific responses in mouse

Eur J Immunol. 2018 Apr;48(4):632-643. doi: 10.1002/eji.201747212. Epub 2018 Jan 18.

Abstract

Oral tolerance can prevent unnecessary immune responses against dietary antigens. Members of the B7 protein family play critical roles in the positive and/or negative regulation of T cell responses to interactions between APCs and T cells. V-set and Ig domain-containing 4 (VSIG4), a B7-related co-signaling molecule, has been known to act as a co-inhibitory ligand and may be critical in establishing immune tolerance. Therefore, we investigated the regulation of VSIG4 signaling in a food allergy and experimental oral tolerance murine models. We analyzed the contributions of the two main sites involved in oral tolerance, the mesenteric lymph node (MLN) and the liver, in VSIG4-mediated oral tolerance induction. Through the comparative analysis of major APCs, dendritic cells (DCs) and macrophages, we found that Kupffer cells play a critical role in inducing regulatory T cells (Tregs) and establishing immune tolerance against oral antigens via VSIG4 signaling. Taken together, these results suggest the possibility of VSIG4 signaling-based regulation of orally administered antigens.

Keywords: F4/80+ cells; Kupffer cell; Oral tolerance; Regulatory T cell; V-set and Ig domain-containing 4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation / metabolism
  • B7 Antigens / immunology
  • Cells, Cultured
  • Dendritic Cells / immunology*
  • Female
  • Immune Tolerance / immunology*
  • Immunoglobulin G / immunology
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / immunology
  • Kupffer Cells / immunology*
  • Liver / cytology
  • Liver / immunology*
  • Lymph Nodes / immunology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Ovalbumin / administration & dosage
  • Ovalbumin / immunology
  • Receptors, CCR7 / genetics
  • Receptors, Complement / genetics
  • Receptors, Complement / immunology*
  • Signal Transduction
  • T-Lymphocytes, Regulatory / immunology*

Substances

  • Antigens, Differentiation
  • B7 Antigens
  • Ccr7 protein, mouse
  • Immunoglobulin G
  • Receptors, CCR7
  • Receptors, Complement
  • VSIG4 protein, mouse
  • monocyte-macrophage differentiation antigen
  • Ovalbumin