Literature DB >> 26004919

How B cells remember? A sophisticated cytoplasmic tail of mIgG is pivotal for the enhanced transmembrane signaling of IgG-switched memory B cells.

Xiangjun Chen1, Gen Li2, Zhengpeng Wan2, Ce Liu2, Yingyue Zeng2, Wanli Liu3.   

Abstract

Antibody memory is critical for protection against many human infectious diseases and is the basis for nearly all current human vaccines. Isotype switched immunoglobulin (Ig) G-expressing memory B cells are considered as one of the fundaments for the rapid, high affinity and high-titered memory antibody response. The detailed molecular mechanism of the enhanced activation of IgG-switched memory B cells upon BCR engagement with antigens has been an elusive question in immunology. In this review, we tried to discuss all the exciting new advances revealing the molecular mechanisms of the transmembrane signaling through mIgG cytoplasmic tail in IgG-switched memory B cells.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  B cell receptor; CD22; Grb2; Memory B cell; SAP97; mIgG cytoplasmic tail

Mesh:

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Year:  2015        PMID: 26004919     DOI: 10.1016/j.pbiomolbio.2015.04.010

Source DB:  PubMed          Journal:  Prog Biophys Mol Biol        ISSN: 0079-6107            Impact factor:   3.667


  2 in total

1.  Transmembrane signaling: A multiplex problem with converging solutions.

Authors:  James J Chou; Jia-huai Wang
Journal:  Prog Biophys Mol Biol       Date:  2015-07-02       Impact factor: 3.667

Review 2.  A cold-blooded view of adaptive immunity.

Authors:  Martin F Flajnik
Journal:  Nat Rev Immunol       Date:  2018-07       Impact factor: 53.106

  2 in total

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