RAG2:GFP knockin mice reveal novel aspects of RAG2 expression in primary and peripheral lymphoid tissues

被引:144
作者
Monroe, RJ
Seidl, KJ
Gaertner, F
Han, SH
Chen, F
Sekiguchi, J
Wang, JY
Ferrini, R
Davidson, L
Kelsoe, G
Alt, FW
机构
[1] Childrens Hosp, Howard Hughes Med Inst, Ctr Blood Res, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[3] Duke Univ, Sch Med, Dept Immunol, Durham, NC 27710 USA
关键词
D O I
10.1016/S1074-7613(00)80095-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We generated mice in which a functional RAG2:GFP fusion gene is knocked in to the endogenous RAG2 locus. In bone marrow and thymus, RAG2:GFP expression occurs in appropriate stages of developing B and T cells as well as in immature bone marrow IgM(+) B cells. RAGS:GFP also is expressed in IgD(+) B cells following cross-linking of IgM on immature IgM(+)IgD(+) B cells generated in vitro. RAG2:GFP expression is undetectable in most immature splenic B cells; however, in young RAG2:GFP mice, there are substantial numbers of splenic RAG2:GFP(+) cells that mostly resemble pre-B cells. The tatter population decreases in size with age but reappears following immunization of older RAG2:GFP mice. We discuss the implications of these findings for current models of receptor assembly and diversification.
引用
收藏
页码:201 / 212
页数:12
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