Department of Virology, Faculty of Medicine, Kyushu University, Maidashi, Higashi-ku, Fukuoka, Japan.
PLoS Pathog. 2012;8(8):e1002857. doi: 10.1371/journal.ppat.1002857. Epub 2012 Aug 9.
Nod-like receptors (NLRs) comprise a large family of intracellular pattern- recognition receptors. Members of the NLR family assemble into large multiprotein complexes, termed the inflammasomes. The NLR family, pyrin domain-containing 3 (NLRP3) is triggered by a diverse set of molecules and signals, and forms the NLRP3 inflammasome. Recent studies have indicated that both DNA and RNA viruses stimulate the NLRP3 inflammasome, leading to the secretion of interleukin 1 beta (IL-1β) and IL-18 following the activation of caspase-1. We previously demonstrated that the proton-selective ion channel M2 protein of influenza virus activates the NLRP3 inflammasome. However, the precise mechanism by which NLRP3 recognizes viral infections remains to be defined. Here, we demonstrate that encephalomyocarditis virus (EMCV), a positive strand RNA virus of the family Picornaviridae, activates the NLRP3 inflammasome in mouse dendritic cells and macrophages. Although transfection with RNA from EMCV virions or EMCV-infected cells induced robust expression of type I interferons in macrophages, it failed to stimulate secretion of IL-1β. Instead, the EMCV viroporin 2B was sufficient to cause inflammasome activation in lipopolysaccharide-primed macrophages. While cells untransfected or transfected with the gene encoding the EMCV non-structural protein 2A or 2C expressed NLRP3 uniformly throughout the cytoplasm, NLRP3 was redistributed to the perinuclear space in cells transfected with the gene encoding the EMCV 2B or influenza virus M2 protein. 2B proteins of other picornaviruses, poliovirus and enterovirus 71, also caused the NLRP3 redistribution. Elevation of the intracellular Ca(2+) level, but not mitochondrial reactive oxygen species and lysosomal cathepsin B, was important in EMCV-induced NLRP3 inflammasome activation. Chelation of extracellular Ca(2+) did not reduce virus-induced IL-1β secretion. These results indicate that EMCV activates the NLRP3 inflammasome by stimulating Ca(2+) flux from intracellular storages to the cytosol, and highlight the importance of viroporins, transmembrane pore-forming viral proteins, in virus-induced NLRP3 inflammasome activation.
核苷酸结合寡聚化结构域样受体(NLRs)是一类广泛存在于细胞内的模式识别受体。NLR 家族的成员组装成大型多蛋白复合物,称为炎性小体。NLR 家族成员,包含 pyrin 结构域的 3(NLRP3),可以被多种分子和信号触发,并形成 NLRP3 炎性小体。最近的研究表明,DNA 和 RNA 病毒都能刺激 NLRP3 炎性小体,导致白细胞介素 1β(IL-1β)和白细胞介素 18(IL-18)在半胱天冬酶 1 的激活后分泌。我们之前已经证明,流感病毒的质子选择性离子通道 M2 蛋白可以激活 NLRP3 炎性小体。然而,NLRP3 识别病毒感染的确切机制仍有待确定。在这里,我们证明,脑炎心肌炎病毒(EMCV),一种正链 RNA 病毒科的小 RNA 病毒,可在小鼠树突状细胞和巨噬细胞中激活 NLRP3 炎性小体。尽管用 EMCV 病毒粒子或感染细胞的 RNA 转染诱导了巨噬细胞中 I 型干扰素的强烈表达,但它未能刺激 IL-1β 的分泌。相反,EMCV 病毒孔蛋白 2B 足以在脂多糖预刺激的巨噬细胞中引起炎性小体的激活。虽然未转染或转染编码 EMCV 非结构蛋白 2A 或 2C 的基因的细胞在细胞质中均匀表达 NLRP3,但在转染编码 EMCV 2B 或流感病毒 M2 蛋白的基因的细胞中,NLRP3 被重新分布到核周空间。其他小 RNA 病毒,脊髓灰质炎病毒和肠道病毒 71 的 2B 蛋白也引起了 NLRP3 的重新分布。细胞内 Ca(2+)水平的升高,但不是线粒体活性氧和溶酶体组织蛋白酶 B,在 EMCV 诱导的 NLRP3 炎性小体激活中很重要。细胞外 Ca(2+)螯合并没有减少病毒诱导的 IL-1β 分泌。这些结果表明,EMCV 通过刺激细胞内储存的 Ca(2+)向细胞质内流来激活 NLRP3 炎性小体,并且突出了跨膜孔形成病毒蛋白,即病毒孔蛋白,在病毒诱导的 NLRP3 炎性小体激活中的重要性。