Institute of Chemical Safety, Chinese Academy of Inspection and Quarantine , Beijing 100124, People's Republic of China.
Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences , Beijing 100085, People's Republic of China.
J Agric Food Chem. 2016 Jul 27;64(29):5909-18. doi: 10.1021/acs.jafc.5b05923. Epub 2016 Jul 15.
Graphene has promising applications in food packaging, water purification, and detective sensors for contamination monitoring. However, the biological effects of graphene are not fully understood. It is necessary to clarify the potential risks of graphene exposure to humans through diverse routes, such as foods. In the present study, graphene, as the model nanomaterial, was used to test its potential effects on the cell proliferation based on multiple representative cell lines, including HepG2, A549, MCF-7, and HeLa cells. Graphene was characterized by Raman spectroscopy, particle size analysis, atomic force microscopy, and transmission electron microscopy. The cellular responses to graphene exposure were evaluated using flow cytometry, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, and alamarBlue assays. Rat cerebral astrocyte cultures, as the non-cancer cells, were used to assess the potential cytotoxicity of graphene as well. The results showed that graphene stimulation enhanced cell proliferation in all tested cell cultures and the highest elevation in cell growth was up to 60%. A western blot assay showed that the expression of epidermal growth factor (EGF) was upregulated upon graphene treatment. The phosphorylation of EGF receptor (EGFR) and the downstream proteins, ShC and extracellular regulating kinase (ERK), were remarkably induced, indicating that the activation of the mitogen-activated protein kinase (MAPK)/ERK signaling pathway was triggered. The activation of PI3 kinase p85 and AKT showed that the PI3K/AKT signaling pathway was also involved in graphene-induced cell proliferation, causing the increase of cell ratios in the G2/M phase. No influences on cell apoptosis were observed in graphene-treated cells when compared to the negative controls, proving the low cytotoxicity of this emerging nanomaterial. The findings in this study revealed the potential cellular biological effect of graphene, which may give useful hints on its biosafety evaluation and the further exploration of the bioapplication.
石墨烯在食品包装、水净化和污染监测的侦探传感器等方面具有广阔的应用前景。然而,石墨烯的生物学效应尚未完全了解。有必要通过多种途径,如食物,阐明石墨烯暴露对人类的潜在风险。在本研究中,使用石墨烯作为模型纳米材料,基于多个代表性细胞系,包括 HepG2、A549、MCF-7 和 HeLa 细胞,测试其对细胞增殖的潜在影响。通过拉曼光谱、粒度分析、原子力显微镜和透射电子显微镜对石墨烯进行了表征。使用流式细胞术、3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐和 alamarBlue 测定评估细胞对石墨烯暴露的反应。大鼠脑星形胶质细胞培养物作为非癌细胞,也用于评估石墨烯的潜在细胞毒性。结果表明,石墨烯刺激可增强所有测试细胞培养物中的细胞增殖,细胞生长的最高升高可达 60%。Western blot 检测表明,石墨烯处理后表皮生长因子 (EGF) 的表达上调。EGF 受体 (EGFR) 和下游蛋白 ShC 和细胞外调节激酶 (ERK) 的磷酸化显著诱导,表明丝裂原活化蛋白激酶 (MAPK)/ERK 信号通路被激活。PI3 激酶 p85 和 AKT 的磷酸化表明 PI3K/AKT 信号通路也参与了石墨烯诱导的细胞增殖,导致 G2/M 期细胞比例增加。与阴性对照组相比,在石墨烯处理的细胞中未观察到细胞凋亡的影响,证明这种新兴纳米材料的细胞毒性较低。本研究结果揭示了石墨烯的潜在细胞生物学效应,这可能为其生物安全性评价和进一步探索生物应用提供有用的线索。