Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA.
Science. 2010 Sep 17;329(5998):1530-4. doi: 10.1126/science.1187029.
Endosomal Toll-like receptors (TLRs) 7 and 9 recognize viral pathogens and induce signals leading to the activation of nuclear factor κB (NF-κB)-dependent proinflammatory cytokines and interferon regulatory factor 7 (IRF7)-dependent type I interferons (IFNs). Recognition of viral nucleic acids by TLR9 requires its cleavage in the endolysosomal compartment. Here, we show that TLR9 signals leading to the activation of type I IFN, but not proinflammatory cytokine genes, require TLR9 trafficking from endosomes to a specialized lysosome-related organelle. Furthermore, we identify adapter protein-3 as the protein complex responsible for the trafficking of TLR9 to this subcellular compartment. Our results reveal an intracellular mechanism for bifurcation of TLR9 signals by selective receptor trafficking within the endosomal system.
内体 Toll 样受体 (TLR) 7 和 9 识别病毒病原体,并诱导导致核因子 κB (NF-κB) 依赖性促炎细胞因子和干扰素调节因子 7 (IRF7) 依赖性 I 型干扰素 (IFN) 的激活的信号。TLR9 识别病毒核酸需要其在内体溶酶体隔室中的切割。在这里,我们表明,导致 I 型 IFN 激活的 TLR9 信号,但不包括促炎细胞因子基因,需要 TLR9 从内体到专门的溶酶体相关细胞器的运输。此外,我们确定衔接蛋白-3 是负责 TLR9 向该细胞内隔室运输的蛋白复合物。我们的结果揭示了内体系统中选择性受体运输对内体 TLR9 信号分叉的细胞内机制。