gp49B-mediated negative regulation of antibody production by memory and marginal zone B cells

J Immunol. 2014 Jul 15;193(2):635-44. doi: 10.4049/jimmunol.1302772. Epub 2014 Jun 16.


The rapid Ab responses observed after primary and secondary immunizations are mainly derived from marginal zone (MZ) and memory B cells, respectively, but it is largely unknown how these responses are negatively regulated. Several inhibitory receptors have been identified and their roles have been studied, but mainly on follicular B cells and much less so on MZ B, and never on memory B cells. gp49B is an Ig superfamily member that contains two ITIMs in its cytoplasmic tail, and it has been shown to negatively regulate mast cell, macrophage, and NK cell responses. In this study, we demonstrate that gp49B is preferentially expressed on memory and MZ B cells. We show that gp49B(-/-) mice produce more IgM after a primary immunization and more IgM and IgG1 after a secondary immunization than gp49B(+/+) mice in T cell-dependent immune responses. Memory and MZ B cells from gp49B(-/-) mice also produce more Abs upon in vitro stimulation with CD40 than those from gp49B(+/+) mice. The in vitro IgM production by MZ B cells from gp49B(+/+), but not gp49B(-/-), mice is suppressed by interaction with a putative gp49B ligand, the integrin αvβ3 heterodimer. In addition, gp49B(-/-) mice exhibited exaggerated IgE production in the memory recall response. These results suggest that plasma cell development from memory and MZ B cells, as well as subsequent Ab production, are suppressed via gp49B. In memory B cells, this suppression also prevents excessive IgE production, thus curtailing allergic diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibody Formation / immunology*
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • BALB 3T3 Cells
  • Cell Differentiation / genetics
  • Cell Differentiation / immunology
  • Cells, Cultured
  • Chickens
  • Ficoll / analogs & derivatives
  • Ficoll / immunology
  • Flow Cytometry
  • Immunization / methods
  • Immunoglobulin E / immunology
  • Immunoglobulin E / metabolism
  • Immunoglobulin G / immunology
  • Immunoglobulin G / metabolism
  • Immunoglobulin M / immunology
  • Immunoglobulin M / metabolism
  • Immunologic Memory / immunology*
  • Integrin alphaVbeta3 / genetics
  • Integrin alphaVbeta3 / immunology
  • Integrin alphaVbeta3 / metabolism
  • Lymphoid Tissue / immunology*
  • Lymphoid Tissue / metabolism
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology*
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Plasma Cells / immunology
  • Plasma Cells / metabolism
  • Protein Binding / immunology
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / immunology*
  • Receptors, Immunologic / metabolism
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • gamma-Globulins / immunology


  • (4-hydroxy-3-nitrophenyl)acetyl-Ficoll
  • Immunoglobulin G
  • Immunoglobulin M
  • Integrin alphaVbeta3
  • Lilrb4 protein, mouse
  • Membrane Glycoproteins
  • Receptors, Immunologic
  • gamma-Globulins
  • Ficoll
  • Immunoglobulin E