Hu Qinglin, Jiao Bao, Shi Xinghua, Valle Russell P, Zuo Yi Y, Hu Guoqing
State Key Laboratory of Nonlinear Mechanics, Beijing Key Laboratory of Engineered Construction and Mechanobiology, Institute of Mechanics, Chinese Academy of Sciences, Beijing 100190, China.
Department of Mechanical Engineering, University of Hawaii at Manoa, Honolulu, Hawaii 96822, USA.
Nanoscale. 2015 Nov 21;7(43):18025-9. doi: 10.1039/c5nr05401j.
Graphene oxide (GO) is the most common derivative of graphene and has been used in a large range of biomedical applications. Despite considerable progress in understanding its cytotoxicity, its potential inhalation toxicity is still largely unknown. As the pulmonary surfactant (PS) film is the first line of host defense, interaction with the PS film determines the fate of the inhaled nanomaterials and their potential toxicity. Using a coarse-grained molecular dynamics model, we reported, for the first time, a novel mechanism of toxicity caused by the inhaled GO nanosheets. Upon deposition, the GO nanosheets induce pores in the PS film and thus have adverse effects on the ultrastructure and biophysical properties of the PS film. Notably, the pores induced by GO nanosheets result in increasing the compressibility of the PS film, which is an important indication of surfactant inhibition. In vitro experiments have also been conducted to study the interactions between GO and animal-derived natural PS films, qualitatively confirming the simulation results.
氧化石墨烯(GO)是石墨烯最常见的衍生物,已被广泛应用于众多生物医学领域。尽管在了解其细胞毒性方面取得了显著进展,但其潜在的吸入毒性仍 largely unknown。由于肺表面活性剂(PS)膜是宿主防御的第一道防线,与PS膜的相互作用决定了吸入纳米材料的命运及其潜在毒性。我们使用粗粒度分子动力学模型首次报道了吸入的GO纳米片引起毒性的新机制。沉积后,GO纳米片在PS膜中诱导形成孔,从而对PS膜的超微结构和生物物理性质产生不利影响。值得注意的是,GO纳米片诱导的孔导致PS膜的压缩性增加,这是表面活性剂抑制的一个重要指标。还进行了体外实验来研究GO与动物源性天然PS膜之间的相互作用,定性地证实了模拟结果。