B cell receptor expression level determines the fate of developing B lymphocytes

Receptor editing versus selection

Valerie Kouskoff, Georges Lacaud, Kathryn Pape, Marc Retter, David Nemazee

Research output: Contribution to journalArticle

63 Citations (Scopus)

Abstract

During B lymphocyte development, antibody genes are assembled by DNA recombination. Successful cell surface expression of IgM promotes developmental progression. However, when antigen receptors bind autoantigen, development is blocked and ongoing antibody gene recombination occurs, which often alters antibody specificity in a process called receptor editing. We demonstrate here a significant role of developmental block and receptor editing in B cell receptor quality control. During development a functional, non-self-reactive receptor undergoes receptor editing if its expression is below a certain threshold. Doubling the receptor gene dose promotes development in the absence of autoantigen, but allows editing when autoantigen is present. Thus, both underexpressed and harmful B cell receptors can undergo correction by receptor editing.

Original languageEnglish (US)
Pages (from-to)7435-7439
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume97
Issue number13
DOIs
StatePublished - Jun 20 2000

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Autoantigens
B-Lymphocytes
Genetic Recombination
Genes
Antigen Receptors
Antibody Specificity
Antibodies
Quality Control
Immunoglobulin M
DNA

Cite this

B cell receptor expression level determines the fate of developing B lymphocytes : Receptor editing versus selection. / Kouskoff, Valerie; Lacaud, Georges; Pape, Kathryn; Retter, Marc; Nemazee, David.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 97, No. 13, 20.06.2000, p. 7435-7439.

Research output: Contribution to journalArticle

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