The Role of the Pre-B Cell Receptor in B Cell Development, Repertoire Selection, and Tolerance

Around four decades ago, it had been observed that there were cell lines as well as cells in the fetal liver that expressed antibody μ heavy (μH) chains in the apparent absence of light chains. It was thus possible that these cells expressed another molecule(s), that assembled with μH chains. The en...

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Published inFrontiers in immunology Vol. 9; p. 2423
Main Authors Winkler, Thomas H., Mårtensson, Inga-Lill
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 15.11.2018
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ISSN1664-3224
1664-3224
DOI10.3389/fimmu.2018.02423

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Summary:Around four decades ago, it had been observed that there were cell lines as well as cells in the fetal liver that expressed antibody μ heavy (μH) chains in the apparent absence of light chains. It was thus possible that these cells expressed another molecule(s), that assembled with μH chains. The ensuing studies led to the discovery of the pre-B cell receptor (pre-BCR), which is assembled from Ig μH and surrogate light (SL) chains, together with the signaling molecules Igα and β. It is expressed on a fraction of pro-B (pre-BI) cells and most large pre-B(II) cells, and has been implicated in IgH chain allelic exclusion and down-regulation of the recombination machinery, assessment of the expressed μH chains and shaping the IgH repertoire, transition from the pro-B to pre-B stage, pre-B cell expansion, and cessation.
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Reviewed by: Bonnie B. Blomberg, University of Miami, United States; Raul M. Torres, University of Colorado, United States
Edited by: Harry W. Schroeder, University of Alabama at Birmingham, United States
This article was submitted to B Cell Biology, a section of the journal Frontiers in Immunology
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2018.02423