Environmental Toxicology Graduate Program, University of California, Riverside, California 92521, United States.
Department of Biochemistry, University of California, Riverside, California 92521, United States.
Chem Res Toxicol. 2022 Jul 18;35(7):1244-1256. doi: 10.1021/acs.chemrestox.2c00042. Epub 2022 Jun 15.
Applications of reduced graphene oxide (rGO) in many different areas have been gradually increasing owing to its unique physicochemical characteristics, demanding more understanding of their biological impacts. Herein, we assessed the toxicological effects of rGO in mammary epithelial cells. Because the as-synthesized rGO was dissolved in sodium cholate to maintain a stable aqueous dispersion, we hypothesize that changing the cholate concentration in the dispersion may alter the surface property of rGO and subsequently affect its cellular toxicity. Thus, four types of rGO were prepared and compared: rGO dispersed in 4 and 2 mg/mL sodium cholate, labeled as rGO and concentrated-rGO (c-rGO), respectively, and rGO and c-rGO coated with a protein corona through 1 h incubation in culture media, correspondingly named pro-rGO and pro-c-rGO. Notably, c-rGO and pro-c-rGO exhibited higher toxicity than rGO and pro-rGO and also caused higher reactive oxygen species production, more lipid membrane peroxidation, and more significant disruption of mitochondrial-based ATP synthesis. In all toxicological assessments, pro-c-rGO induced more severe adverse impacts than c-rGO. Further examination of the material surface, protein adsorption, and cellular uptake showed that the surface of c-rGO was coated with a lower content of surfactant and adsorbed more proteins, which may result in the higher cellular uptake observed with pro-c-rGO than pro-rGO. Several proteins involved in cellular redox mediation were also more enriched in pro-c-rGO. These results support the strong correlation between dispersant coating and corona formation and their subsequent cellular impacts. Future studies in this direction could reveal a deeper understanding of the correlation and the specific cellular pathways involved and help gain knowledge on how the toxicity of rGO could be modulated through surface modification, guiding the sustainable applications of rGO.
由于还原氧化石墨烯(rGO)具有独特的物理化学特性,其在许多不同领域的应用逐渐增加,因此需要更多地了解其生物影响。在此,我们评估了 rGO 在乳腺上皮细胞中的毒理学效应。由于合成的 rGO 溶解在胆酸钠中以保持稳定的水相分散体,我们假设改变分散体中的胆酸钠浓度可能会改变 rGO 的表面性质,从而影响其细胞毒性。因此,我们制备并比较了四种类型的 rGO:分别标记为 rGO 和浓缩-rGO(c-rGO)的 rGO 分散在 4 和 2mg/mL 胆酸钠中,以及通过在培养基中孵育 1 小时分别被蛋白质冠包裹的 rGO 和 c-rGO,分别命名为 pro-rGO 和 pro-c-rGO。值得注意的是,c-rGO 和 pro-c-rGO 的毒性比 rGO 和 pro-rGO 更高,并且还导致更高的活性氧产生、更多的脂质膜过氧化以及更显著的线粒体 ATP 合成破坏。在所有毒理学评估中,pro-c-rGO 引起的不利影响比 c-rGO 更严重。对材料表面、蛋白质吸附和细胞摄取的进一步检查表明,c-rGO 的表面覆盖有较低含量的表面活性剂并吸附了更多的蛋白质,这可能导致与 pro-rGO 相比,pro-c-rGO 具有更高的细胞摄取率。还发现几种参与细胞氧化还原调节的蛋白质在 pro-c-rGO 中更为丰富。这些结果支持了分散剂涂层和冠形成及其随后的细胞影响之间的强相关性。在这一方向的未来研究可能会揭示更深层次的相关性以及涉及的特定细胞途径,并有助于了解如何通过表面改性来调节 rGO 的毒性,从而指导 rGO 的可持续应用。