Wnt signaling regulates B lymphocyte proliferation through a LEF-1 dependent mechanism

被引:358
|
作者
Reya, T
O'Riordan, M
Okamura, R
Devaney, E
Willert, K
Nusse, R
Grosschedl, R
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Stanford Univ, Dept Dev Biol, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
关键词
D O I
10.1016/S1074-7613(00)00004-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lymphocyte enhancer factor-1 (LEF-1) is a member of the LEF-1/TCF family of transcription factors, which have been implicated in Wnt signaling and tumorigenesis. LEF-1 was originally identified in pre-B and T cells, but its function in B lymphocyte development remains unknown. Here we report that LEF-1-deficient mice exhibit defects in pro-B cell proliferation and survival in vitro and in vivo. We further show that Lef1(-/-) pro-B cells display elevated levels of fas and c-myc transcription, providing a potential mechanism for their increased sensitivity to apoptosis. Finally, we establish a link between Wnt signaling and normal B cell development by demonstrating that Wnt proteins are mitogenic for pro-B cells and that this effect is mediated by LEF-1.
引用
收藏
页码:15 / 24
页数:10
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