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Gene deregulation and chronic activation in natural killer cells deficient in the transcription factor ETS1

机译:在转录因子ETS1中缺乏的自然杀伤细胞中基因放松抑制和慢性激活

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摘要

Multiple transcription factors guide the development of mature functional natural killer (NK) cells yet little is known about their function. We used global gene expression and genome wide-binding analyses combined with developmental and functional studies to unveil three roles for the ETS1 transcription factor in NK cells. ETS1 functions at the earliest stages of NK cell development to promote expression of critical transcriptional regulators including T-BET and ID2, NK cell receptors (NKRs) including NKp46, Ly49H and Ly49D and signaling molecules essential for NKR function. As a consequence, Ets1−/− NK cells fail to degranulate after stimulation through activating NKRs. Nonetheless, these cells are hyper-responsive to cytokines and have characteristics of chronic stimulation including increased expression of inhibitory NKRs and multiple activation-associated genes. Therefore, ETS1 regulates a broad gene expression program in NK cells that promotes target cell recognition while limiting cytokine driven activation.
机译:多转录因子指导成熟功能自然杀伤(NK)细胞的发展尚未知道其功能。我们使用全局基因表达和基因组宽结合分析与发育和功能研究结合,以揭示NK细胞中ETS1转录因子的三个作用。 ETS1在NK细胞开发的最早阶段起作用,促进临界转录调节剂的表达,包括T-BET和ID2,NK细胞受体(NKR),包括NKP46,LY49H和LY49D和对NKR功能所必需的信号分子。结果,ETS1 - / - / - / - NK细胞通过激活NKRS刺激后不能降低。尽管如此,这些细胞对细胞因子具有超响应性,并且具有慢性刺激的特征,包括增加抑制性NKR和多种激活相关基因的表达。因此,ETS1调节NK细胞中的宽基因表达程序,其在限制细胞因子驱动激活时促进靶细胞识别。

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