Somatic activation of β-catenin bypasses pre-TCR signaling and TCR selection in thymocyte development

被引:154
|
作者
Gounari, F
Aifantis, I
Khazaie, K
Hoeflinger, S
Harada, N
Taketo, MM
von Boehmer, H
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA
[2] Merck, Banyu Tsukuba Res Inst, Tsukuba, Ibaraki 3002611, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Pharmacol, Sakyo Ku, Kyoto 6068501, Japan
关键词
D O I
10.1038/ni0901-863
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mutation or ablation of T cell factor I and lymphocyte enhancer factor I indicated involvement of the Wnt pathway in thymocyte development. The central effector of the Wnt pathway is beta -catenin, which undergoes stabilization upon binding of Wnt ligands to frizzled receptors. We report here that conditional stabilization of beta -catenin in immature thymocytes resulted in the generation of single positive T cells that lacked the alpha beta TCR and developed in the absence of pre-TCR signaling and TCR selection. Although active beta -catenin induced differentiation in the absence of TCRs, its action was associated with reduced proliferation and survival when compared to developmental changes induced by the pre-TCR or the alpha beta TCR.
引用
收藏
页码:863 / 869
页数:7
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