CD40 expression and function in murine B cell ontogeny

被引:23
作者
Castigli, E
Young, F
Carossino, AM
Alt, FW
Geha, RS
机构
[1] HARVARD UNIV,CHILDRENS HOSP,HOWARD HUGHES MED INST,CTR BLOOD RES,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,DEPT GENET,BOSTON,MA 02115
[3] HARVARD UNIV,SCH MED,DEPT PEDIAT,BOSTON,MA 02115
关键词
B cell precursors; B cell transgenics; lymphoid development; RAG-2-deficient mice;
D O I
10.1093/intimm/8.3.405
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The CD40 antigen, a member of the nerve growth factor/tumor necrosis factor receptor family, is expressed on all mature B lymphocytes and plays a crucial role in B cell activation, T cell-dependent antigen-driven isotype switching and germinal center formation, We have analyzed CD40 expression and function during mouse B cell development by examining B cell precursors in normal mice and in transgenic animals in which B cell development is frozen at discrete stages, These models included RAG-2(-/-) mice, and transgenic littermates that express a mu heavy chain and/or the bcl-2 proto-oncogene transgene, CD40 was undetectable at the pro-B cell stage, but was expressed, although at low levels, on pre-B cells, However, pre-B cells failed to respond to CD40 triggering either by expression of CD23 or by proliferation in the presence of IL-4. Overexpression of bcl-2 increased the density of CD40 expression on pre-B cells: these cells respond to CD40 ligation by expressing CD23 and by proliferating in the presence of IL-4.
引用
收藏
页码:405 / 411
页数:7
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