Cecil Jessica D, O'Brien-Simpson Neil M, Lenzo Jason C, Holden James A, Singleton William, Perez-Gonzalez Alexis, Mansell Ashley, Reynolds Eric C
Oral Health CRC, Melbourne Dental School, Bio21 Institute, The University of Melbourne, Melbourne, VIC, Australia.
Department of Molecular and Translational Science, Monash University, Clayton, VIC, Australia.
Front Immunol. 2017 Aug 25;8:1017. doi: 10.3389/fimmu.2017.01017. eCollection 2017.
Outer membrane vesicles (OMVs) are proteoliposomes blebbed from the surface of Gram-negative bacteria. Chronic periodontitis is associated with an increase in subgingival plaque of Gram-negative bacteria, , and . In this study, we investigated the immune-modulatory effects of , and OMVs on monocytes and differentiated macrophages. All of the bacterial OMVs were phagocytosed by monocytes, M(naïve) and M(IFNγ) macrophages in a dose-dependent manner. They also induced NF-κB activation and increased TNFα, IL-8, and IL-1β cytokine secretion. OMVs were also found to induce anti-inflammatory IL-10 secretion. Although unprimed monocytes and macrophages were resistant to OMV-induced cell death, lipopolysaccharide or OMV priming resulted in a significantly reduced cell viability. , and OMVs all activated inflammasome complexes, as monitored by IL-1β secretion and ASC speck formation. ASC was critical for OMV-induced inflammasome formation, while AIM2-/- and Caspase-1-/- cells had significantly reduced inflammasome formation and NLRP3-/- cells exhibited a slight reduction. OMVs were also found to provide both priming and activation of the inflammasome complex. High-resolution microscopy and flow cytometry showed that OMVs primed and activated macrophage inflammasomes with 80% of macrophages exhibiting inflammasome complex formation. In conclusion, periodontal pathogen OMVs were found to have significant immunomodulatory effects upon monocytes and macrophages and should therefore influence pro-inflammatory host responses associated with disease.
外膜囊泡(OMVs)是从革兰氏阴性菌表面泡出的蛋白脂质体。慢性牙周炎与革兰氏阴性菌龈下菌斑增加有关,以及。在本研究中,我们调查了、和OMVs对单核细胞和分化巨噬细胞的免疫调节作用。所有细菌OMVs均被单核细胞、M(幼稚)和M(IFNγ)巨噬细胞以剂量依赖方式吞噬。它们还诱导NF-κB活化并增加TNFα、IL-8和IL-1β细胞因子分泌。还发现OMVs诱导抗炎性IL-10分泌。尽管未致敏的单核细胞和巨噬细胞对OMV诱导的细胞死亡具有抗性,但脂多糖或OMV致敏导致细胞活力显著降低。、和OMVs均激活炎性小体复合物,通过IL-1β分泌和ASC斑点形成监测。ASC对OMV诱导的炎性小体形成至关重要,而AIM2 - / - 和Caspase - 1 - / - 细胞的炎性小体形成显著减少,NLRP3 - / - 细胞表现出轻微减少。还发现OMVs提供炎性小体复合物的致敏和激活。高分辨率显微镜和流式细胞术显示,OMVs致敏并激活巨噬细胞炎性小体,80%的巨噬细胞表现出炎性小体复合物形成。总之,发现牙周病原体OMVs对单核细胞和巨噬细胞具有显著的免疫调节作用,因此应影响与疾病相关的促炎宿主反应。