Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
PLoS One. 2013 Nov 6;8(11):e77955. doi: 10.1371/journal.pone.0077955. eCollection 2013.
Mycoplasma hyorhinis (M.hyorhinis, M.hy) is associated with development of gastric and prostate cancers. The NLRP3 inflammasome, a protein complex controlling maturation of important pro-inflammatory cytokines interleukin (IL)-1β and IL-18, is also involved in tumorigenesis and metastasis of various cancers.
METHODOLOGY/PRINCIPAL FINDINGS: To clarify whether M.hy promoted tumor development via inflammasome activation, we analyzed monocytes for IL-1β and IL-18 production upon M.hy challenge. When exposed to M.hy, human monocytes exhibited rapid and robust IL-1β and IL-18 secretion. We further identified that lipid-associated membrane protein (LAMP) from M.hy was responsible for IL-1β induction. Applying competitive inhibitors, gene specific shRNA and gene targeted mice, we verified that M.hy induced IL-1β secretion was NLRP3-dependent in vitro and in vivo. Cathepsin B activity, K(+) efflux, Ca(2+) influx and ROS production were all required for the NLRP3 inflammasome activation by M.hy. Importantly, it is IL-1β but not IL-18 produced from macrophages challenged with M.hy promoted gastric cancer cell migration and invasion.
Our data suggest that activation of the NLRP3 inflammasome by M.hy may be associated with its promotion of gastric cancer metastasis, and anti-M.hy therapy or limiting NLRP3 signaling could be effective approach for control of gastric cancer progress.
支原体(M.hyorhinis,M.hy)与胃癌和前列腺癌的发展有关。NLRP3 炎性小体是一种控制重要促炎细胞因子白细胞介素 (IL)-1β 和 IL-18 成熟的蛋白复合物,也参与各种癌症的肿瘤发生和转移。
方法/主要发现:为了阐明 M.hy 是否通过炎性小体激活促进肿瘤发展,我们分析了 M.hy 挑战后单核细胞中 IL-1β 和 IL-18 的产生。当暴露于 M.hy 时,人单核细胞表现出快速而强烈的 IL-1β 和 IL-18 分泌。我们进一步确定 M.hy 的脂质相关膜蛋白 (LAMP) 负责诱导 IL-1β。应用竞争抑制剂、基因特异性 shRNA 和基因靶向小鼠,我们验证了 M.hy 在体外和体内诱导的 IL-1β 分泌依赖于 NLRP3。溶酶体蛋白酶 B 活性、K(+) 外流、Ca(2+) 内流和 ROS 产生都是 M.hy 激活 NLRP3 炎性小体所必需的。重要的是,是巨噬细胞受到 M.hy 刺激后产生的 IL-1β 而不是 IL-18 促进了胃癌细胞的迁移和侵袭。
我们的数据表明,M.hy 激活 NLRP3 炎性小体可能与其促进胃癌转移有关,抗 M.hy 治疗或限制 NLRP3 信号可能是控制胃癌进展的有效方法。