1 INFETTARE, Facultad de Medicina, Universidad Cooperativa de Colombia, Medellín, Colombia.
2 Grupo Inmunovirología, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Innate Immun. 2017 Nov;23(8):697-708. doi: 10.1177/1753425917738331.
In recent years, the potential use of silica nanoparticles (SiNPs) among different biomedical fields has grown. A deep understanding of the physicochemical properties of nanoparticles (NPs) and their regulation of specific biological responses is crucial for the successful application of NPs. Exposure to NP physicochemical properties (size, shape, porosity, etc.) could result in deleterious effects on cellular functions, including a pro-inflammatory response mediated via activation of the NLRP3 inflammasome. The aim of this study was to evaluate the potential in vitro immunomodulatory effect of 12-nm and 200-nm SiNPs on the expression of pro-inflammatory cytokines and NLRP3 inflammasome components in human primary neutrophils and PBMCs. This study demonstrates that regardless of the size of the nanoparticles, SiNPs induce the production of pro-inflammatory cytokines in a dose-dependent manner. Induced IL-1β production after exposure to SiNPs suggests the involvement of NLRP3 inflammasome components participation in this process. In conclusion, SiNPs induce the production of pro-inflammatory cytokines in a dose-dependent manner. Furthermore, our data suggest that the production and release of IL-1β possibly occurs through the formation of the NLRP3 inflammasome.
近年来,硅纳米颗粒(SiNPs)在不同的生物医学领域的潜在用途不断增加。深入了解纳米颗粒(NPs)的物理化学性质及其对特定生物反应的调节作用对于 NPs 的成功应用至关重要。暴露于 NP 的物理化学性质(大小、形状、孔隙率等)可能会对细胞功能产生有害影响,包括通过激活 NLRP3 炎性体介导的促炎反应。本研究旨在评估 12nm 和 200nm SiNPs 对人原代中性粒细胞和 PBMCs 中促炎细胞因子和 NLRP3 炎性体成分表达的潜在体外免疫调节作用。本研究表明,无论纳米颗粒的大小如何,SiNPs 均可诱导促炎细胞因子的产生呈剂量依赖性。SiNPs 暴露后诱导产生的 IL-1β 表明 NLRP3 炎性体成分参与了这一过程。总之,SiNPs 可诱导促炎细胞因子的产生呈剂量依赖性。此外,我们的数据表明,IL-1β 的产生和释放可能通过 NLRP3 炎性体的形成发生。