Assessment of genotoxicity induced by subchronic exposure to graphene in HaCaT human skin cell line.

Autor: Frontiñan-Rubio J; Medical School, University of Castilla-La Mancha, Ciudad Real, Spain.; CRIB, Centro Regional de Investigaciones Biomédicas, Universidad de Castilla-La Mancha, Ciudad Real, Spain., García-Carpintero S; Medical School, University of Castilla-La Mancha, Ciudad Real, Spain.; CRIB, Centro Regional de Investigaciones Biomédicas, Universidad de Castilla-La Mancha, Ciudad Real, Spain., González VJ; Instituto Regional de Investigación Científica Aplicada (IRICA), University of Castilla-La Mancha, Ciudad Real, Spain., Vázquez E; Instituto Regional de Investigación Científica Aplicada (IRICA), University of Castilla-La Mancha, Ciudad Real, Spain.; Faculty of Chemical Science and Technology, Universidad de Castilla-La Mancha, Ciudad Real, Spain., Durán-Prado M; Medical School, University of Castilla-La Mancha, Ciudad Real, Spain.; CRIB, Centro Regional de Investigaciones Biomédicas, Universidad de Castilla-La Mancha, Ciudad Real, Spain.
Jazyk: angličtina
Zdroj: Nanotoxicology [Nanotoxicology] 2023 Feb; Vol. 17 (1), pp. 42-61. Date of Electronic Publication: 2023 Mar 11.
DOI: 10.1080/17435390.2023.2183653
Abstrakt: The applications of graphene-based materials (GBMs) and their processing involve prolonged contact with cellular barriers such as human skin. Even though the potential cytotoxicity of graphene has been studied in recent years, the impact of long-term graphene exposure has rarely been explored. We tested in the HaCaT epithelial cells, in vitro , the effect of subchronic treatments with sublethal doses of four different, well-characterized GBMs, two commercial graphene oxides (GO) and two few-layer graphenes (FLG). Cells were exposed weekly to low doses of the GBMs for 14 days, 30 days, 3 months, and 6 months. GBMs-cells uptake was assessed by confocal microscopy. Cell death and cell cycle were determined by fluorescence microscopy and cytometry. DNA damage was measured by comet assay and γ-H2AX staining, followed by the determination of p-p53 and p-ATR by immunolabeling. Subchronic exposure to different GBMs at noncytotoxic doses has potential genotoxic effects on HaCaT epithelial cells that can be recovered depending on the GBM and exposure time. Specifically, GO-induced genotoxicity can be detected after 14 and 30 days from treatment. At this time, FLG appears less genotoxic than GO, and cells can recover more quickly when genotoxic pressure disappears after some days of removal of the GBM. Long-term exposure, 3 and 6 months, to different GBMs induces permanent, nonreversible, genotoxic damage comparable to the exerted by arsenite. This should be considered for the production and future applications of GBMs in scenarios where low concentrations of the material interact chronically with epithelial barriers.
Databáze: MEDLINE
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