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首页> 外文期刊>Nature Communications >Glycogen synthase kinase 3β ubiquitination by TRAF6 regulates TLR3-mediated pro-inflammatory cytokine production
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Glycogen synthase kinase 3β ubiquitination by TRAF6 regulates TLR3-mediated pro-inflammatory cytokine production

机译:糖原合酶激酶3β被TRAF6泛素化调节TLR3介导的促炎性细胞因子的产生

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摘要

TRAF6 is critical for the production of inflammatory cytokines in various TLR-mediated signalling pathways. However, it is poorly understood how TRAF6 regulates TLR3 responses. Here we demonstrate that GSK3β interacts with TRAF6 and positively regulates the TLR3 -mediated signalling. Suppression of GSK3β expression or its kinase activity drastically reduces the production of inflammatory cytokines and the induction of c-Fos by decreasing ERK and p38 phosphorylation. GSK3β physically associates with TRAF6 in a TLR3 ligand poly I:C-dependent manner. TRAF6 is determined to be a direct E3 ligase for GSK3β , and TRAF6 -mediated GSK3β ubiquitination is essential for poly I:C-dependent cytokine production by promoting the TLR3 adaptor protein TRIF -assembled signalling complex.
机译:TRAF6对于各种TLR介导的信号传导途径中炎性细胞因子的产生至关重要。但是,人们对TRAF6如何调节TLR3反应的了解却很少。在这里,我们证明GSK3β与TRAF6相互作用并正向调节TLR3介导的信号传导。通过减少ERK和p38磷酸化,抑制GSK3β表达或其激酶活性可大大减少炎症细胞因子的产生和c-Fos的诱导。 GSK3β以TLR3配体poly I:C依赖性方式与TRAF6物理缔合。已确定TRAF6是GSK3β的直接E3连接酶,并且TRAF6介导的GSK3β泛素化通过促进TLR3衔接蛋白TRIF组装的信号复合物,对聚I:C依赖性细胞因子的产生至关重要。

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