Herzog Eva, Byrne Hugh J, Casey Alan, Davoren Maria, Lenz Anke-Gabriele, Maier Konrad L, Duschl Albert, Oostingh Gertie Janneke
Radiation and Environmental Science Centre (RESC), Focas Institute, Dublin Institute of Technology, Kevin Street, Dublin 8, Ireland.
Toxicol Appl Pharmacol. 2009 Feb 1;234(3):378-90. doi: 10.1016/j.taap.2008.10.015. Epub 2008 Nov 7.
Single-walled carbon nanotubes have gained enormous popularity due to a variety of potential applications which will ultimately lead to increased human and environmental exposure to these nanoparticles. This study was carried out in order to evaluate the inflammatory response of immortalised and primary human lung epithelial cells (A549 and NHBE) to single-walled carbon nanotube samples (SWCNT). Special focus was placed on the mediating role of lung surfactant on particle toxicity. The toxicity of SWCNT dispersed in cell culture medium was compared to that of nanotubes dispersed in dipalmitoylphosphatidylcholine (DPPC, the main component of lung lining fluid). Exposure was carried out for 6 to 48 h with the latter time-point showing the most significant responses. Moreover, exposure was performed in the presence of the pro-inflammatory stimulus tumour necrosis factor-alpha (TNF-alpha) in order to mimic exposure of stimulated cells, as would occur during infection. Endpoints evaluated included cell viability, proliferation and the analysis of inflammatory mediators such as interleukin (IL)-8, IL-6, TNF-alpha and macrophage chemoattractant protein-1 (MCP-1). Crocidolite asbestos was included as a well characterised, toxic fibre control. The results of this study showed that HiPco SWCNT samples suppress inflammatory responses of A549 and NHBE cells. This was also true for TNF-alpha stimulated cells. The use of DPPC improved the degree of SWCNT dispersion in A549 medium and in turn, leads to increased particle toxicity, however, it was not shown to modify NHBE cell responses.
单壁碳纳米管因其具有多种潜在应用而广受欢迎,这些应用最终将导致人类和环境对这些纳米颗粒的接触增加。本研究旨在评估永生化和原代人肺上皮细胞(A549和NHBE)对单壁碳纳米管样品(SWCNT)的炎症反应。特别关注肺表面活性剂在颗粒毒性中的介导作用。将分散在细胞培养基中的SWCNT的毒性与分散在二棕榈酰磷脂酰胆碱(DPPC,肺内衬液的主要成分)中的纳米管的毒性进行比较。暴露时间为6至48小时,后者时间点显示出最显著的反应。此外,在促炎刺激物肿瘤坏死因子-α(TNF-α)存在的情况下进行暴露,以模拟受刺激细胞的暴露,就像感染期间会发生的那样。评估的终点包括细胞活力、增殖以及对炎症介质如白细胞介素(IL)-8、IL-6、TNF-α和巨噬细胞趋化蛋白-1(MCP-1)的分析。将青石棉作为一种特征明确的有毒纤维对照物纳入研究。本研究结果表明,HiPco SWCNT样品可抑制A549和NHBE细胞的炎症反应。对于TNF-α刺激的细胞也是如此。使用DPPC可改善SWCNT在A549培养基中的分散程度,进而导致颗粒毒性增加,然而,并未显示其会改变NHBE细胞的反应。