Asakura Yusuke, Fujiwara Yoshihiro, Kato Naoko, Sato Yuko, Komatsu Toru
Department of Anesthesiology, Aichi Medical University, Nagoya, Japan.
Am J Hematol. 2007 Jul;82(7):640-2. doi: 10.1002/ajh.20817.
Cells of the innate immune system discriminate between "noninfectious self" and "infectious nonself" via pattern recognition receptors known as Toll-like receptors (TLRs). Though TLRs and the related interleukin 1 receptors share considerable homology in their cytoplasmic domains and adaptor molecules, signaling cascades may substantially differ from one another depending on the adaptor proteins recruited. Here we show that ectopic overexpression of catalytically inactive dominant-negative PKR expression system suppressed NF- kappa B activation mediated by TLR3, TLR9, TNF receptor 1 and 2 (TNF-R 1/2), but not by TLR4. Physiological relevance of the observations described here are discussed.
先天性免疫系统的细胞通过被称为Toll样受体(TLR)的模式识别受体来区分“非感染性自身”和“感染性非自身”。尽管TLR和相关的白细胞介素1受体在其细胞质结构域和衔接分子中具有相当大的同源性,但信号级联可能会因所招募的衔接蛋白而有很大差异。在这里,我们表明催化失活的显性负性PKR表达系统的异位过表达抑制了由TLR3、TLR9、肿瘤坏死因子受体1和2(TNF-R 1/2)介导的NF-κB激活,但不抑制TLR4介导的NF-κB激活。本文讨论了此处所述观察结果的生理相关性。