Outer Membrane Vesicles Prime and Activate Macrophage Inflammasomes and Cytokine Secretion In Vitro and In Vivo

• Published in: Frontiers in immunology 2017-08, Vol.8, p.1017-1017
• Main Authors: Cecil, Jessica D, O'Brien-Simpson, Neil M, Lenzo, Jason C, Holden, James A, Singleton, William, Perez-Gonzalez, Alexis, Mansell, Ashley, Reynolds, Eric C
• Format: Article
• Language: English
• Subjects: Immunology; inflammasomes; macrophages; outer membrane vesicles; Porphyromonas gingivalis; Tannerella forsythia; Treponema denticola
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2017.01017

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.