等离子体电池
生物
B细胞
分泌物
抗体
B-1电池
记忆B细胞
幼稚B细胞
抗原
分子生物学
CD40
细胞生物学
免疫学
T细胞
抗原提呈细胞
体外
免疫系统
内分泌学
细胞毒性T细胞
遗传学
作者
Miriam A. Shelef,Kuo‐I Lin,Louise J. McHeyzer‐Williams,Jerry Liao,Michael G. McHeyzer‐Williams,Kathryn Calame
出处
期刊:Immunity
[Elsevier]
日期:2003-10-01
卷期号:19 (4): 607-620
被引量:790
标识
DOI:10.1016/s1074-7613(03)00267-x
摘要
Blimp-1 is a transcriptional repressor able to drive the terminal differentiation of B cells into Ig-secreting plasma cells. We have created mice with a B cell-specific deletion of prdm1, the gene encoding Blimp-1. B cell development and the number of B cells responding to antigen appear to be normal in these mice. However, in response to either TD or TI antigen, serum Ig, short-lived plasma cells, post-GC plasma cells, and plasma cells in a memory response are virtually absent, demonstrating that Blimp-1 is required for plasmacytic differentiation and Ig secretion. In the absence of Blimp-1, CD79b+B220− pre-plasma memory B cell development is also defective, providing evidence that this subset is an intermediate in plasma cell development. B cells lacking Blimp-1 cannot secrete Ig or induce μS mRNA when stimulated ex vivo. Furthermore, although prdm1−/− B cells fail to induce XBP-1, XBP-1 cannot rescue plasmacytic differentiation without Blimp-1.
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