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β-连环蛋白的体细胞激活在胸腺细胞发育过程中绕过了前T细胞受体信号传导和T细胞受体选择。

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

作者信息

Gounari F, Aifantis I, Khazaie K, Hoeflinger S, Harada N, Taketo M M, von Boehmer H

机构信息

Department of Pathology, Harvard Medical School, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

出版信息

Nat Immunol. 2001 Sep;2(9):863-9. doi: 10.1038/ni0901-863.

Abstract

Mutation or ablation of T cell factor 1 and lymphocyte enhancer factor 1 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.

摘要

T细胞因子1和淋巴细胞增强因子1的突变或缺失表明Wnt信号通路参与胸腺细胞发育。Wnt信号通路的核心效应分子是β-连环蛋白,当Wnt配体与卷曲受体结合时,β-连环蛋白会发生稳定化。我们在此报告,未成熟胸腺细胞中β-连环蛋白的条件性稳定导致产生缺乏αβTCR的单阳性T细胞,且这些细胞在没有前TCR信号和TCR选择的情况下发育。尽管活性β-连环蛋白在没有TCR的情况下诱导分化,但其作用与前TCR或αβTCR诱导的发育变化相比,增殖和存活能力降低。

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