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Review
. 2003;27(2-3):309-30.
doi: 10.1385/IR:27:2-3:309.

Role of the BCR complex in B cell development, activation, and leukemic transformation

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Review

Role of the BCR complex in B cell development, activation, and leukemic transformation

Susan R Rheingold et al. Immunol Res. 2003.

Abstract

A primary focus of signal transduction in B cells, from the pre-B cell to the mature B cell, is the B cell receptor complex. Here we describe work demonstrating the importance of signaling via the pre-B cell receptor complex (pre-BCR) to the pre-B cell transition, the central checkpoint in B-cell development. We have shown tht pre-BCR complex components Igalpha and Igbeta are critical to allowing the pre-B cell to move through this transition, but may not be required for allelic exclusion. Pre-BCR expression also directly affects the response of leukemic cells to steroid treatment, suggesting that signals initiated by the pre-BCR complex may present therapeutic targets in acute leukemia. Additionally, interleukin-7 may also modulate the response of leukemic cells arising from early B-cell stages to treatment. This observation has lead directly to proposals to test drugs which may antagonize early B-cell growth signals, such as rapamycin, in acute lymphoid leukemia.

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References

    1. Curr Opin Cell Biol. 1995 Apr;7(2):163-75 - PubMed
    1. Int Immunol. 1993 Jun;5(6):647-56 - PubMed
    1. Proc Natl Acad Sci U S A. 1985 Dec;82(24):8658-62 - PubMed
    1. Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):474-8 - PubMed
    1. Nature. 1990 Jun 28;345(6278):810-3 - PubMed

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