Vercammen Elisabeth, Staal Jens, Beyaert Rudi
Department for Molecular Biomedical Research, VIB, Ghent, Belgium.
Clin Microbiol Rev. 2008 Jan;21(1):13-25. doi: 10.1128/CMR.00022-07.
Toll-like receptors (TLRs) form a major group of transmembrane receptors that are involved in the detection of invading pathogens. Double-stranded RNA is a marker for viral infection that is recognized by TLR3. TLR3 triggering activates specific signaling pathways that culminate in the activation of NF-kappaB and IRF3 transcription factors, as well as apoptosis, enabling the host to mount an effective innate immune response through the induction of cytokines, chemokines, and other proinflammatory mediators. In this review, we describe the paradoxical role of TLR3 in innate immunity against different viruses and in viral pathogenesis but also the evidence for TLR3 as a "danger" receptor in nonviral diseases. We also discuss the structure and cellular localization of TLR3, as well as the complex signaling and regulatory events that contribute to TLR3-mediated immune responses.
Toll样受体(TLRs)构成了一类主要的跨膜受体,参与检测入侵的病原体。双链RNA是病毒感染的标志物,可被TLR3识别。TLR3的激活会启动特定的信号通路,最终导致核因子κB(NF-κB)和干扰素调节因子3(IRF3)转录因子的激活以及细胞凋亡,从而使宿主通过诱导细胞因子、趋化因子和其他促炎介质来启动有效的先天性免疫反应。在本综述中,我们描述了TLR3在针对不同病毒的先天性免疫和病毒发病机制中的矛盾作用,以及TLR3作为非病毒疾病中“危险”受体的证据。我们还讨论了TLR3的结构和细胞定位,以及促成TLR3介导的免疫反应的复杂信号传导和调节事件。