Department of Microbiology and Immunology, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan.
J Biol Chem. 2011 Mar 4;286(9):7043-51. doi: 10.1074/jbc.M110.164632. Epub 2010 Dec 28.
The innate immune system elicits the first wave of immune responses against pathogen infection. Its operational modes are complex and have yet to be defined. Here, we report the identification of an innate immune regulator termed TAPE (TBK1-associated protein in endolysosomes), previously known as CC2D1A/Freud-1/Aki-1, which modulates the TLR3 and TLR4 pathways. We found that TAPE activated the TBK1, NF-κB, and ERK pathways leading to IFN-β and inflammatory cytokine induction. TAPE was shown to colocalize with endosomal marker Rab5 and lysosomal marker LAMP1 in mammalian cells, suggesting that TAPE resided in endolysosomes. Knockdown of TAPE selectively impaired the TLR3 and endocytic TLR4 pathways to IFN-β induction. Furthermore, TAPE interacted and synergized with Trif to activate IFN-β. TAPE knockdown failed to block Trif-mediated IFN-β induction, whereas Trif knockdown impaired the TLR3 and TAPE cooperation on IFN-β induction, suggesting that TAPE acts upstream of Trif. Together, our data demonstrate a central role for TAPE in linking TLR3 and TLR4 to innate immune defenses at an early step.
先天免疫系统引发了针对病原体感染的第一波免疫反应。其运作模式复杂,尚未得到明确界定。在这里,我们报告了一种先天免疫调节剂的鉴定,称为 TAPE(内体中的 TBK1 相关蛋白),以前称为 CC2D1A/Freud-1/Aki-1,它调节 TLR3 和 TLR4 途径。我们发现 TAPE 激活了 TBK1、NF-κB 和 ERK 途径,导致 IFN-β 和炎症细胞因子的诱导。TAPE 被证明与内体标记物 Rab5 和溶酶体标记物 LAMP1 在哺乳动物细胞中共定位,表明 TAPE 位于内体溶酶体中。TAPE 的敲低选择性地损害了 TLR3 和内吞 TLR4 途径对 IFN-β 的诱导。此外,TAPE 与 Trif 相互作用并协同激活 IFN-β。TAPE 敲低不能阻断 Trif 介导的 IFN-β 诱导,而 Trif 敲低则损害了 TLR3 和 TAPE 在 IFN-β 诱导上的合作,表明 TAPE 在前 Trif 阶段起作用。总之,我们的数据表明 TAPE 在将 TLR3 和 TLR4 连接到先天免疫防御的早期步骤中起着核心作用。