Redundant functions of TCF-1 and LEF-1 during T and NK cell development, but unique role of TCF-1 for Ly49 NK cell receptor acquisition

被引:56
作者
Held, W
Clevers, H
Grosschedl, R
机构
[1] Ludwig Inst Canc Res, Lausanne Branch, CH-1066 Epalinges, Switzerland
[2] Univ Lausanne, CH-1066 Epalinges, Switzerland
[3] Ctr Biomed Genet, Hubrecht Lab, Utrecht, Netherlands
[4] Univ Munich, Gene Ctr, Munich, Germany
[5] Univ Munich, Inst Biochem, Munich, Germany
关键词
T cell; NK cell; TCF-1; LEF-1; Ly49;
D O I
10.1002/eji.200323840
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Members of the TCF/LEF (T cell factor / lymphoid enhancer factor) family of DNA-binding factors play important roles during embryogenesis, the establishment and/or maintenance of self-renewing tissues such as the immune system and for malignant transformation. Specifically, it has been shown that TCF-1 is required for T cell development. A role for LEF-1 became apparent when mice harbored two hypomorphic TCF-1 alleles and consequently expressed low levels of TCF-1. Here we show that NK cell development is similarly regulated by redundant functions of TCF-1 and LEF-1, whereby TCF-1 contributes significantly more to NK cell development than LEF-1. Despite this role for INK cell development, LEF-1 is not required for the establishment of a repertoire of MHC class I-specific Ly49 receptors on INK cells. The proper formation of this repertoire depends to a large extent on TCF-1. These findings suggest common and distinct functions of TCF-1 and LEF-1 during lymphocyte development.
引用
收藏
页码:1393 / 1398
页数:6
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