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mTORC1 信号通过诱导 TIRAP 表达来控制 TLR2 介导的 T 细胞激活。

mTORC1 Signaling Controls TLR2-Mediated T-Cell Activation by Inducing TIRAP Expression.

机构信息

Laboratory for Cell Signaling, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Kanagawa 230-0045, Japan.

Laboratory for Cell Signaling, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Kanagawa 230-0045, Japan.

出版信息

Cell Rep. 2020 Jul 21;32(3):107911. doi: 10.1016/j.celrep.2020.107911.

Abstract

Effector, but not naïve, T cells are activated by toll-like receptor-2 (TLR2) stimulation, leading to cytokine production and proliferation. We found that the differential response is attributable to the lack of expression of the adaptor protein TIRAP in naive T cells. TIRAP expression is induced upon T-cell receptor (TCR) stimulation and sustained by strong interleukin-2 (IL-2) signals. Expression of TIRAP requires TCR- and IL-2-induced mTORC1 activation. TLR2 stimulation induced the activation of nuclear factor κB (NF-κB) and ERK, leading to much higher production of interferon-γ (IFN-γ) by T helper 1 (Th1) cells cultured in a high concentration of IL-2 than by those cultured in a low concentration of IL-2. In contrast, TLR2 stimulation induces mTORC1 activation through TIRAP, which is essential for TLR2-mediated IFN-γ production. These data demonstrate that the mTORC1 signal confers the response to TLR2 signaling by inducing TIRAP expression and that the TIRAP-mTORC1 axis is critical for TLR2-mediated IFN-γ production by effector T cells.

摘要

效应器 T 细胞而非幼稚 T 细胞可被 Toll 样受体 2(TLR2)刺激激活,从而导致细胞因子的产生和增殖。我们发现,这种差异反应归因于幼稚 T 细胞中衔接蛋白 TIRAP 的表达缺失。TIRAP 的表达在 T 细胞受体(TCR)刺激后被诱导,并受到强烈的白细胞介素 2(IL-2)信号的持续作用。TIRAP 的表达需要 TCR 和 IL-2 诱导的 mTORC1 激活。TLR2 刺激诱导核因子 κB(NF-κB)和 ERK 的激活,导致在高浓度 IL-2 中培养的 Th1 细胞产生的干扰素-γ(IFN-γ)比在低浓度 IL-2 中培养的细胞产生的 IFN-γ 高出许多。相比之下,TLR2 刺激通过 TIRAP 诱导 mTORC1 激活,这对于 TLR2 介导的 IFN-γ 产生是必需的。这些数据表明,mTORC1 信号通过诱导 TIRAP 表达赋予对 TLR2 信号的反应,并且 TIRAP-mTORC1 轴对于效应器 T 细胞中 TLR2 介导的 IFN-γ 产生至关重要。

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