Laboratory of Ion Channel Research, Department of Cellular and Molecular Medicine, VIB Center for Brain & Disease Research, Herestraat 49, 3000 Leuven, Belgium.
Int J Mol Sci. 2021 Sep 21;22(18):10173. doi: 10.3390/ijms221810173.
Because of their low cost and easy production, silica nanoparticles (SiNPs) are widely used in multiple manufacturing applications as anti-caking, densifying and hydrophobic agents. However, this has increased the exposure levels of the general population and has raised concerns about the toxicity of this nanomaterial. SiNPs affect the function of the airway epithelium, but the biochemical pathways targeted by these particles remain largely unknown. Here we investigated the effects of SiNPs on the responses of 16HBE14o- cultured human bronchial epithelial (16HBE) cells to the damage-associated molecular pattern ATP, using fluorometric measurements of intracellular Ca concentration. Upon stimulation with extracellular ATP, these cells displayed a concentration-dependent increase in intracellular Ca, which was mediated by release from intracellular stores. SiNPs inhibited the Ca responses to ATP within minutes of application and at low micromolar concentrations, which are significantly faster and more potent than those previously reported for the induction of cellular toxicity and pro-inflammatory responses. SiNPs-induced inhibition is independent from the increase in intracellular Ca they produce, is largely irreversible and occurs via a non-competitive mechanism. These findings suggest that SiNPs reduce the ability of airway epithelial cells to mount ATP-dependent protective responses.
由于成本低、生产简单,硅纳米颗粒(SiNPs)被广泛应用于多种制造领域,用作抗结块剂、致密剂和疏水剂。然而,这增加了普通人群的暴露水平,并引发了人们对这种纳米材料毒性的担忧。SiNPs 会影响气道上皮细胞的功能,但这些颗粒靶向的生化途径在很大程度上仍不清楚。在这里,我们使用细胞内 Ca 浓度的荧光测量法,研究了 SiNPs 对培养的人支气管上皮细胞(16HBE)对损伤相关分子模式 ATP 反应的影响。在细胞外 ATP 的刺激下,这些细胞表现出浓度依赖性的细胞内 Ca 增加,这是通过细胞内储存的释放来介导的。SiNPs 在应用后的几分钟内以低微摩尔浓度抑制了对 ATP 的 Ca 反应,其速度明显快于先前报道的诱导细胞毒性和促炎反应的速度,作用也更强。SiNPs 诱导的抑制作用与它们产生的细胞内 Ca 增加无关,在很大程度上是不可逆的,并且通过非竞争性机制发生。这些发现表明,SiNPs 降低了气道上皮细胞产生依赖于 ATP 的保护反应的能力。