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J Exp Med. 2004 Apr 19;199(8):1101-12. Epub 2004 Apr 12.

Receptor editing and marginal zone B cell development are regulated by the helix-loop-helix protein, E2A.

Author information

1
Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.

Abstract

Previous studies have indicated that the E2A gene products are required to initiate B lineage development. Here, we demonstrate that E2A(+/-) B cells that express an autoreactive B cell receptor fail to mature due in part to an inability to activate secondary immunoglobulin (Ig) light chain gene rearrangement. Both RAG1/2 gene expression and RS deletion are severely defective in E2A(+/-) mice. Additionally, we demonstrate that E2A(+/-) mice show an increase in the proportion of marginal zone B cells with a concomitant decrease in the proportion of follicular B cells. In contrast, Id3-deficient splenocytes show a decline in the proportion of marginal zone B cells. Based on these observations, we propose that E-protein activity regulates secondary Ig gene rearrangement at the immature B cell stage and contributes to cell fate determination of marginal zone B cells. Additionally, we propose a model in which E-proteins enforce the developmental checkpoint at the immature B cell stage.

PMID:
15078898
PMCID:
PMC2211894
DOI:
10.1084/jem.20031180
[Indexed for MEDLINE]
Free PMC Article

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