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Fli-1 regulates the DN2 to DN3 thymocyte transition and promotes γδ T-cell commitment by enhancing TCR signal strength

机译:Fli-1调节的DN2 DN3胸腺细胞过渡,促进γδt细胞的承诺增强细胞信号强度

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摘要

Friend leukemia integration 1 (Fli-1) is a member of the Ets transcription factor family and is expressed during T-cell development; however, the role Fli-1 plays in early T-cell differentiation has not been elucidated. In this report, we demonstrate that in mouse, Fli-1 overexpression retards the CD4-CD8- double-negative (DN) to CD4+CD8+ doublepositive (DP) transition by deregulating normal DN thymocyte development. Specifically, Fli-1 expression moderates the DN2 and DN3 developmental transitions. We further show that Fli-1 overexpression partially mimics strong TCR signals in developing DN thymocytes and thereby enhances γδ T-cell development. Conversely, Fli-1 knockdown by small hairpin RNA reverses the lineage bias from γδ T cells and directs DN cells to the αβ lineage by attenuating TCR signaling. Therefore, Fli-1 plays a critical role in both the DN2 to DN3 transition and αβ/γδ lineage commitment.
机译:朋友白血病集成1 (Fli-1)是一个成员Ets的转录因子家族,表达了在t细胞发育;Fli-1早期t细胞分化中的作用尚未阐明。证明在鼠标,Fli-1超表达阻碍CD4-CD8——双重否定(DN)CD4 + CD8 + doublepositive (DP)过渡解除对DN胸腺细胞的正常发展。具体来说,温和派的DN2 Fli-1表达式和DN3发展转换。表明Fli-1超表达部分模仿强大的发展中DN胸腺细胞识别信号从而增强γδt细胞的发展。相反,小发夹RNA Fli-1击倒逆转的血统的偏见γδT细胞指导DN细胞αβ衰减血统细胞信号传导。作用在DN2 DN3过渡和αβ/γδ血统的承诺。

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