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Nuclear Factor of Activated T Cells Transcription Factor Nfatp Controls Superantigen-Induced Lethal Shock

机译:激活的T细胞的转录因子Nfatp的核因子控制超抗原诱导的致命性休克

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摘要

Tumor necrosis factor α (TNF-α) is the key mediator of superantigen-induced T cell lethal shock. Here, we show that nuclear factor of activated T cells transcription factor, NFATp, controls susceptibility to superantigen-induced lethal shock in mice through its activation of TNF-α gene transcription. In NFATp-deficient mice, T cell stimulation leads to delayed induction and attenuation of TNF-α mRNA levels, decreased TNF-α serum levels, and resistance to superantigen-induced lethal shock. By contrast, after lipopolysaccharide (LPS) challenge, serum levels of TNF-α and susceptibility to shock are unaffected. These results demonstrate that NFATp is an essential activator of immediate early TNF-α gene expression in T cells and they present in vivo evidence of the inducer- and cell type–specific regulation of TNF-α gene expression. Furthermore, they suggest NFATp as a potential selective target in the treatment of superantigen-induced lethal shock.
机译:肿瘤坏死因子α(TNF-α)是超抗原诱导的T细胞致死性休克的关键介质。在这里,我们显示激活的T细胞转录因子NFATp的核因子通过激活TNF-α基因转录来控制小鼠对超抗原诱发的致命性休克的敏感性。在NFATp缺陷型小鼠中,T细胞刺激导致TNF-αmRNA水平的诱导和减弱,TNF-α血清水平降低以及对超抗原诱导的致命性休克的抵抗。相比之下,脂多糖(LPS)攻击后,血清TNF-α水平和休克易感性均未受影响。这些结果表明,NFATp是T细胞中立即早期TNF-α基因表达的重要激活剂,它们提供了TNF-α基因表达的诱导物和细胞类型特异性调节的体内证据。此外,他们建议NFATp作为超抗原诱导的致死性休克的治疗中潜在的选择性靶标。

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