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氧化石墨烯和还原氧化石墨烯通过ERK信号通路诱导神经嗜铬细胞瘤衍生的PC12细胞系凋亡和细胞周期改变。

Graphene oxide and reduced graphene oxide induced neural pheochromocytoma-derived PC12 cell lines apoptosis and cell cycle alterations via the ERK signaling pathways.

作者信息

Kang Yiyuan, Liu Jia, Wu Junrong, Yin Qian, Liang Huimin, Chen Aijie, Shao Longquan

机构信息

Nanfang Hospital, Southern Medical University, Guangzhou, People's Republic of China.

出版信息

Int J Nanomedicine. 2017 Aug 2;12:5501-5510. doi: 10.2147/IJN.S141032. eCollection 2017.

Abstract

Given the novel applications of graphene materials in biomedical and electronics industry, the health hazards of these particles have attracted extensive worldwide attention. Although many studies have been performed on graphene material-induced toxic effects, toxicological data for the effect of graphene materials on the nervous system are lacking. In this study, we focused on the biological effects of graphene oxide (GO) and reduced graphene oxide (rGO) materials on PC12 cells, a type of traditional neural cell line. We found that GO and rGO exerted significant toxic effects on PC12 cells in a dose- and time-dependent manner. Moreover, apoptosis appeared to be a response to toxicity. A potent increase in the number of PC12 cells at G0/G1 phase after GO and rGO exposure was detected by cell cycle analysis. We found that phosphorylation levels of ERK signaling molecules, which are related to cell cycle regulation and apoptosis, were significantly altered after GO and rGO exposure. In conclusion, our results show that GO has more potent toxic effects than rGO and that apoptosis and cell cycle arrest are the main toxicity responses to GO and rGO treatments, which are likely due to ERK pathway regulation.

摘要

鉴于石墨烯材料在生物医学和电子工业中的新型应用,这些颗粒对健康的危害已引起全球广泛关注。尽管已经对石墨烯材料诱导的毒性作用进行了许多研究,但关于石墨烯材料对神经系统影响的毒理学数据仍然缺乏。在本研究中,我们聚焦于氧化石墨烯(GO)和还原氧化石墨烯(rGO)材料对PC12细胞(一种传统神经细胞系)的生物学效应。我们发现,GO和rGO对PC12细胞具有显著的剂量和时间依赖性毒性作用。此外,凋亡似乎是对毒性的一种反应。通过细胞周期分析检测到,GO和rGO暴露后,处于G0/G1期的PC12细胞数量显著增加。我们发现,与细胞周期调控和凋亡相关的ERK信号分子的磷酸化水平在GO和rGO暴露后发生了显著改变。总之,我们的结果表明,GO比rGO具有更强的毒性作用,并且凋亡和细胞周期停滞是对GO和rGO处理的主要毒性反应,这可能是由于ERK途径的调控所致。

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