Petnicki-Ocwieja Tanja, Kern Aurelie, Killpack Tess L, Bunnell Stephen C, Hu Linden T
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA 02111; and.
Department of Integrative Physiology and Pathobiology, Tufts University School of Medicine, Boston, MA 02111.
J Immunol. 2015 Nov 1;195(9):4331-40. doi: 10.4049/jimmunol.1501268. Epub 2015 Sep 30.
Innate immune engagement results in the activation of host defenses that produce microbe-specific inflammatory responses. A long-standing interest in the field of innate immunity is to understand how varied host responses are generated through the signaling of just a limited number of receptors. Recently, intracellular trafficking and compartmental partitioning have been identified as mechanisms that provide signaling specificity for receptors by regulating signaling platform assembly. We show that cytokine activation as a result of TLR2 stimulation occurs at different intracellular locations and is mediated by the phagosomal trafficking molecule adaptor protein-3 (AP-3). AP-3 is required for trafficking TLR2 purified ligands or the Lyme disease causing bacterium, Borrelia burgdorferi, to LAMP-1 lysosomal compartments. The presence of AP-3 is necessary for the activation of cytokines such as IL-6 but not TNF-α or type I IFNs, suggesting induction of these cytokines occurs from a different compartment. Lack of AP-3 does not interfere with the recruitment of TLR signaling adaptors TRAM and MyD88 to the phagosome, indicating that the TLR-MyD88 signaling complex is assembled at a prelysosomal stage and that IL-6 activation depends on proper localization of signaling molecules downstream of MyD88. Finally, infection of AP-3-deficient mice with B. burgdorferi resulted in altered joint inflammation during murine Lyme arthritis. Our studies further elucidate the effects of phagosomal trafficking on tailoring immune responses in vitro and in vivo.
固有免疫激活会引发宿主防御反应,产生针对微生物的特异性炎症反应。固有免疫领域长期以来的一个研究兴趣是,了解仅通过有限数量的受体信号传导如何产生多样的宿主反应。最近,细胞内运输和区室化分配已被确定为通过调节信号平台组装为受体提供信号特异性的机制。我们发现,Toll样受体2(TLR2)刺激导致的细胞因子激活发生在不同的细胞内位置,且由吞噬体运输分子衔接蛋白3(AP-3)介导。AP-3是将TLR2纯化配体或导致莱姆病的伯氏疏螺旋体运输至溶酶体相关膜蛋白1(LAMP-1)溶酶体区室所必需的。AP-3的存在对于白细胞介素6(IL-6)等细胞因子的激活是必需的,但对肿瘤坏死因子-α(TNF-α)或I型干扰素则不是,这表明这些细胞因子的诱导发生在不同的区室。缺乏AP-3并不干扰TLR信号衔接蛋白TRAM和髓样分化因子88(MyD88)募集至吞噬体,这表明TLR-MyD88信号复合物在溶酶体前阶段组装,且IL-6激活取决于MyD88下游信号分子的正确定位。最后,用伯氏疏螺旋体感染AP-3缺陷小鼠会导致小鼠莱姆关节炎期间关节炎症改变。我们的研究进一步阐明了吞噬体运输在体外和体内对定制免疫反应的影响。