Abstract
As one of the typical actinide elements, the chemical and radioactive toxicities of uranium have attracted more attention. In this work, the toxicity mechanism of uranium-238 in HK-2 cells was studied in detail using in vitro approach. The results confirmed that exposure to uranium solution significantly reduced the viability of HK-2 cells. Flow cytometry and double fluorescence AO/PI staining suggested that apoptosis was the main cause of the death of HK-2 cells. Moreover, reactive oxygen species and mitochondrial membrane potential tests further demonstrated that HK-2 cells underwent apoptosis under the combined action of oxidative stress and mitochondrial damage. The tails in the comet assay and the abnormal nuclear morphology in DAPI staining confirmed the genotoxicity of uranium to HK-2 cells. In conclusion, uranium mainly causes apoptosis and genotoxicity after exposure, and the main mechanisms of apoptosis are mainly related to oxidative stress, mitochondrial damage, and DNA damage.
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Acknowledgements
Financial support was obtained from the National Natural Science Foundation of China (22276084 and 21906073), the “Youth Innovation Promotion Association of the Chinese Academy of Sciences”, and the Fundamental Research Funds for the Central Universities (lzujbky-2022-32)
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Qiang, S., Guo, K., Zhang, D. et al. The damage mechanism of uranium(VI) to HK-2 cells. J Radioanal Nucl Chem 332, 1277–1285 (2023). https://doi.org/10.1007/s10967-023-08843-2
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DOI: https://doi.org/10.1007/s10967-023-08843-2