Du Ziyun, Wei Lai, Murti Aruna, Pfeffer Susan R, Fan Meiyun, Yang Chuan He, Pfeffer Lawrence M
Department of Pathology and Laboratory Medicine, University of Tennessee Health Science Center, University of Tennessee Cancer Institute, Memphis, Tennessee 38163, USA.
J Cell Biochem. 2007 Dec 1;102(5):1087-94. doi: 10.1002/jcb.21535.
Type I interferons (IFNs) regulate diverse cellular functions by modulating the expression of IFN-stimulated genes (ISGs) through the activation of the well established signal transduction pathway of the Janus Kinase (JAK) and signal transducers and activators of transcription (STAT) proteins. Although the JAK-STAT signal transduction pathway is critical in mediating IFN's antiviral and antiproliferative activities, other signaling pathways are activated by IFNs and regulate cellular response to IFN. The NF-kappaB transcription factor regulates the expression of genes involved in cell survival and immune responses. We have identified a novel IFN mediated signal pathway that leads to NF-kappaB activation and demonstrate that a subset of ISGs that play key roles in cellular response to IFN is regulated by NF-kappaB. This review focuses on the IFN-induced NF-kappaB activation pathway and the role of NF-kappaB in ISG expression, antiviral activity and apoptosis, and the therapeutic application of IFN in cancer and infectious disease.
I型干扰素(IFNs)通过激活已确立的Janus激酶(JAK)信号转导途径和转录信号转导子及激活子(STAT)蛋白来调节干扰素刺激基因(ISGs)的表达,从而调控多种细胞功能。尽管JAK-STAT信号转导途径在介导IFN的抗病毒和抗增殖活性中至关重要,但其他信号通路也会被IFNs激活并调节细胞对IFN的反应。核因子κB(NF-κB)转录因子调节参与细胞存活和免疫反应的基因表达。我们鉴定出了一条新的IFN介导的信号通路,该通路可导致NF-κB激活,并证明在细胞对IFN的反应中起关键作用的一部分ISGs受NF-κB调控。本综述聚焦于IFN诱导的NF-κB激活途径以及NF-κB在ISG表达、抗病毒活性和细胞凋亡中的作用,以及IFN在癌症和传染病治疗中的应用。