Differential effect of an Ig μ transgene on development of pre-B cells in fetal and adult SCID mice

被引:5
作者
Bosma, GC
Chang, Y
Karasuyama, H
Bosma, MJ
机构
[1] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[2] Arizona State Univ, Dept Microbiol, Tempe, AZ 85287 USA
[3] Tokyo Metropolitan Inst Med Sci, Dept Immunol, Tokyo 31822, Japan
关键词
B cell differentiation;
D O I
10.1073/pnas.96.21.11952
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Progression of pro-B lymphocytes to the pre-B stage depends on the expression of a pre-B cell receptor (pre-BCR), consisting of an 1g mu H chain, Ig surrogate light chain, and associated signal transducing chains. Mice that are unable to express a pre-BCR show an arrest of B cell development at the pro-B stage. Such is the case for severe combined immune deficient (SCID) mice in which mu chains are not made because of a defect in V(D)J recombination. When mu chains are made, as in SCID mice bearing a functional mu transgene, then B cell differentiation can proceed to the pre-B stage, However, as reported here, a mu transgene (M54) that promotes development of SCID pre-B cells in adult bone marrow fails to do so in fetal liver, We suggest that a pre-BCR containing the M54 mu chain cannot signal progression of pro-B cells to the pre-B stage in the fetal liver microenvironment.
引用
收藏
页码:11952 / 11957
页数:6
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