Verstrepen L, Bekaert T, Chau T-L, Tavernier J, Chariot A, Beyaert R
Department of Molecular Biology, Ghent University, Technologiepark 927, 9052, Ghent, Belgium.
Cell Mol Life Sci. 2008 Oct;65(19):2964-78. doi: 10.1007/s00018-008-8064-8.
Toll-like receptors (TLRs) as well as the receptors for tumor necrosis factor (TNF-R) and interleukin-1 (IL-1R) play an important role in innate immunity by regulating the activity of distinct transcription factors such as nuclear factor-kappaB (NF-kappaB). TLR, IL-1R and TNF-R signaling to NF-kappaB converge on a common IkappaB kinase complex that phosphorylates the NF-kappaB inhibitory protein IkappaBalpha. However, upstream signaling components are in large part receptor-specific. Nevertheless, the principles of signaling are similar, involving the recruitment of specific adaptor proteins and the activation of kinase cascades in which protein-protein interactions are controlled by poly-ubiquitination. In this review, we will discuss our current knowledge of NF-kappaB signaling in response to TLR-4, TNF-R and IL-1R stimulation, with a special focus on the similarities and dissimilarities among these pathways.
Toll样受体(TLRs)以及肿瘤坏死因子受体(TNF-R)和白细胞介素-1受体(IL-1R)通过调节不同转录因子如核因子κB(NF-κB)的活性,在固有免疫中发挥重要作用。TLR、IL-1R和TNF-R向NF-κB的信号传导汇聚于一个共同的IκB激酶复合物,该复合物使NF-κB抑制蛋白IκBα磷酸化。然而,上游信号成分在很大程度上是受体特异性的。尽管如此,信号传导的原理是相似的,包括招募特定的衔接蛋白和激活激酶级联反应,其中蛋白质-蛋白质相互作用由多聚泛素化控制。在这篇综述中,我们将讨论目前关于NF-κB信号传导对TLR-4、TNF-R和IL-1R刺激反应的认识,特别关注这些途径之间的异同。