4.5 Article

Biological Impacts of Reduced Graphene Oxide Affected by Protein Corona Formation

Journal

CHEMICAL RESEARCH IN TOXICOLOGY
Volume 35, Issue 7, Pages 1244-1256

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrestox.2c00042

Keywords

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Funding

  1. National Institute of Environmental Health Sciences (NIEHS) as part of the Nanotechnology Health Implications Research Consortium [U01ES027293]
  2. NIEHS [U24ES026946]
  3. Research Training Grant in Environmental Toxicology - NIEHS [T32ES018827]
  4. UC- Hispanic Serving Institutions Doctoral Diversity Initiative (UC-HIS DDI) award
  5. National Institutes of Health [T34GM062756]
  6. Institute for Integrative Genome Biology Proteomics Core at the University of California-Riverside (UCR) - NIH [S10 OD010669]
  7. UCR Stem Cell Core Facility

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This study assessed the toxic effects of reduced graphene oxide (rGO) on mammary epithelial cells and found that rGO dissolved in sodium cholate may influence cellular toxicity. Surface-modified c-rGO exhibited higher toxicity, oxidative stress, and mitochondrial disruption compared to rGO, indicating a strong correlation between dispersant coating and cellular impacts.
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 concentratedrGO (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 prorGO 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-crGO 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.

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