SiO2 nanoparticles as disruptors of endogenous resolution mechanisms of inflammatory responses that exacerbate pneumonia

Abstract

Occupational exposure to engineered nanomaterials (ENMs) is increasing in the workplace and can impact human health. Amorphous silicon dioxide nanoparticles (SiO₂ NPs) are widely produced respirable ENMs used in commercial products. We have investigated their impact on lung inflammation resolution and bacterial defense. Mice exposed to SiO₂ NPs, followed by bacteria, exhibited increased lung inflammation, bacterial proliferation, and lung damage compared to mice not exposed to NPs. SiO₂ NPs increased human macrophage production of pro-inflammatory mediators and disrupted phagocytosis of bacteria and efferocytosis of apoptotic neutrophils - pivotal responses for host defense and inflammation resolution. A pro-resolving mediator, resolvin D5 (RvD5), restored macrophage phagocytosis of bacteria and partially controlled excess lung inflammation after SiO₂ NPs. These findings demonstrate that SiO₂ NPs disrupt endogenous resolution processes to give rise to heightened lung inflammation and infection. RvD5 reduced inflammation and partially restored endogenous resolution cellular processes, suggesting that RvD5 can reduce ENP disruption of resolution.

Keywords: Infection; Macrophages; Phagocytosis.; Resolution; Resolvin D5; SiO2 nanoparticles.