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BAFF-R expression correlates with positive selection of immature B cells
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 1193846
Author(s) Tussiwand, Roxane; Rauch, Melanie; Flück, Lukas A; Rolink, Antonius G
Author(s) at UniBasel Rolink, Antonius G.
Tussiwand, Roxane
Year 2012
Title BAFF-R expression correlates with positive selection of immature B cells
Journal European journal of immunology
Volume 42
Number 1
Pages / Article-Number 206-16
Keywords BAFF-R, Immature B cells, Mature B cells, Receptor editing, Transitional B cells
Abstract The interaction between BAFF and BAFF-R is crucial for the development of mature B cells. Here, we report that the expression of BAFF-R is first detectable on a fraction of mouse CD19(+) CD93(+) IgM(+) CD23(-) and human CD19(+) CD10(+) IgM(+) BM B cells. This BAFF-R(+) BM B-cell population shows higher levels of surface IgM expression and decreased RAG-2 transcripts than BAFF-R(-) immature B cells. When cultured, mouse BAFF-R(-), but not BAFF-R(+) immature B cells spontaneously undergo B-cell receptor editing. However, BAFF-R(+) immature B cells cultured in the presence of an anti-kappa light chain antibody are induced to undergo receptor editing. This receptor editing correlates with down-modulation of surface BAFF-R expression and the up-regulation of RAG-2 at the RNA level. B-cell receptor (BCR) cross-linking on splenic T1 B cells results in down-modulation of the BAFF-R, and receptor editing and RAG-2 up-regulation in a minor fraction of B cells. BCR cross-linking on splenic T2/3 B cells results in partly down and partly up-modulation of BAFF-R expression and no evidence for receptor editing. Overall, our data indicate that BAFF-R expression is tightly regulated during B-cell development in mouse and human and its expression is correlated with positive selection.
Publisher Verlag Chemie
ISSN/ISBN 0014-2980
edoc-URL http://edoc.unibas.ch/dok/A6004084
Full Text on edoc No
Digital Object Identifier DOI 10.1002/eji.201141957
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/22028296
ISI-Number WOS:000298596600023
Document type (ISI) Journal Article
 
   

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