B-CELL DEVELOPMENT IS PERTURBED IN BONE-MARROW FROM C-FOS/V-JUN DOUBLY TRANSGENIC MICE

被引:14
作者
FUJITA, K
MIKI, N
MOJICA, MP
TAKAO, S
PHUCHAREON, J
NISHIKAWA, S
SUDO, T
TOKUHISA, T
机构
[1] KOBE UNIV,SCH MED,ICMR,DEPT IMMUNOL,7-5-1 KUSUNOKI CHO,CHUO KU,KOBE 650,JAPAN
[2] TORAY INDUSTRIES LTD,BASIC RES LABS,KAMAKURA 248,JAPAN
[3] KUMAMOTO UNIV,SCH MED,DEPT IMMUNOPATHOL,KUMAMOTO 860,JAPAN
关键词
AP-1; C-JUN; IL-7; STROMAL CELLS;
D O I
10.1093/intimm/5.2.227
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
c-fos and c-jun gene products form a heterodimeric complex (AP-1) that regulates target gene expression by binding to a specific DNA sequence motif. In order to study a role of AP-1 (Fos/Jun) in growth and differentiation of immature B lineage cells, we have established and mated two independent transgenic mice carrying the mouse c-fos gene or the viral v-jun gene fused to the H-2K promoter. IL-7 dependent bone marrow cell culture from doubly transgenic (H2-fos/jun) mice demonstrated severe delay of early B cell development. Proliferation of pre-B cells in the fresh bone marrow from H2-fos/jun mice to IL-7 stimulation was very low. These results suggest that the deregulated production of AP-1 perturbs IL-7 mediated proliferation and differentiation of immature B cells.
引用
收藏
页码:227 / 230
页数:4
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