A Distinct Signaling Pathway Used by the IgG-Containing B Cell Antigen Receptor

Author:

Wakabayashi Chisato1,Adachi Takahiro1,Wienands Jürgen2,Tsubata Takeshi1

Affiliation:

1. Department of Immunology, Medical Research Institute, Tokyo Medical and Dental University, 113-8510 Tokyo, Japan.

2. Department of Molecular Immunology, Biology III, Freiburg University and Max-Planck-Institute for Immunobiology, D-79108 Freiburg, Germany.

Abstract

The immunoglobulin G (IgG)–containing B lymphocyte antigen receptor (IgG-BCR) transmits a signal distinct from that of IgM-BCR or IgD-BCR, although all three use the same signal-transducing component, Igα/Igβ. Here we demonstrate that the inhibitory coreceptor CD22 down-modulates signaling through IgM-BCR and IgD-BCR, but not that through IgG-BCR, because of the IgG cytoplasmic tail, which prevents CD22 phosphorylation. These results suggest that the cytoplasmic tail of IgG specifically enhances IgG-BCR signaling by preventing CD22-mediated signal inhibition. Enhanced signaling through IgG-BCR may be involved in efficient IgG production, which is crucial for immunity to pathogens.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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