Aberrant B cell development and immune response in mice with a compromised BCR complex

被引:245
作者
Torres, RM
Flaswinkel, H
Reth, M
Rajewsky, K
机构
[1] UNIV COLOGNE,INST GENET,D-50931 COLOGNE,GERMANY
[2] MAX PLANCK INST IMMUNOBIOL,D-79108 FREIBURG,GERMANY
关键词
D O I
10.1126/science.272.5269.1804
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
The immunoglobulin alpha (Ig-alpha)-Ig-beta heterodimer is the signaling component of the antigen receptor complex on B cells (BCR) and B cell progenitors (pre-BCR). A mouse mutant that lacks most of the Ig-alpha cytoplasmic tail exhibits only a small impairment in early B cell development but a severe block in the generation of the peripheral B cell pool, revealing a checkpoint in B cell maturation that ensures the expression of a functional BCR on mature B cells. B cells that do develop demonstrate a differential dependence on Ig-alpha signaling in antibody responses such that a signaling-competent Ig-alpha appears to be critical for the response to T-independent, but not T-dependent, antigens.
引用
收藏
页码:1804 / 1808
页数:5
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