Honda Kenya, Yanai Hideyuki, Mizutani Tatsuaki, Negishi Hideo, Shimada Naoya, Suzuki Nobutaka, Ohba Yusuke, Takaoka Akinori, Yeh Wen-Chen, Taniguchi Tadatsugu
Department of Immunology, Graduate School of Medicine and Faculty of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
Proc Natl Acad Sci U S A. 2004 Oct 26;101(43):15416-21. doi: 10.1073/pnas.0406933101. Epub 2004 Oct 18.
Toll-like receptor (TLR) activation is central to immunity, wherein the activation of the TLR9 subfamily members TLR9 and TLR7 results in the robust induction of type I IFNs (IFN-alpha/beta) by means of the MyD88 adaptor protein. However, it remains unknown how the TLR signal "input" can be processed through MyD88 to "output" the induction of the IFN genes. Here, we demonstrate that the transcription factor IRF-7 interacts with MyD88 to form a complex in the cytoplasm. We provide evidence that this complex also involves IRAK4 and TRAF6 and provides the foundation for the TLR9-dependent activation of the IFN genes. The complex defined in this study represents an example of how the coupling of the signaling adaptor and effector kinase molecules together with the transcription factor regulate the processing of an extracellular signal to evoke its versatile downstream transcriptional events in a cell. Thus, we propose that this molecular complex may function as a cytoplasmic transductional-transcriptional processor.
Toll样受体(TLR)激活是免疫的核心,其中TLR9亚家族成员TLR9和TLR7的激活通过MyD88衔接蛋白导致I型干扰素(IFN-α/β)的强烈诱导。然而,TLR信号“输入”如何通过MyD88进行处理以“输出”IFN基因的诱导仍不清楚。在这里,我们证明转录因子IRF-7与MyD88相互作用,在细胞质中形成复合物。我们提供的证据表明,该复合物还涉及IRAK4和TRAF6,并为IFN基因的TLR9依赖性激活奠定了基础。本研究中定义的复合物代表了信号衔接子和效应激酶分子与转录因子如何耦合以调节细胞外信号的处理,从而在细胞中引发其多样的下游转录事件的一个例子。因此,我们提出这种分子复合物可能作为一种细胞质转导-转录处理器发挥作用。