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Neuron and glial cells exposed to cerium dioxide nanoparticles: results from MTT and γH2AX assays
* 1, 2 , 1, 2 , 3 , 4, 5, 6 , 4, 5, 6 , 4, 5, 6 , 4, 5, 6 , 2, 7 , 2, 7 , 1, 2
1  Universidade da Coruña, Grupo NanoToxGen, Centro Interdisciplinar de Química e Bioloxía - CICA, Departamento de Biología, Facultad de Ciencias, Campus A Zapateira s/n, 15071, A Coruña, Spain
2  Instituto de Investigación Biomédica de A Coruña (INIBIC). Oza, 15071 A Coruña, Spain
3  Universidade da Coruña, Departamento de Biología, Facultad de Ciencias, Campus A Zapateira s/n, 15071, A Coruña, Spain
4  EPIUnit - Instituto de Saúde Pública, Universidade do Porto, Rua das Taipas, nº 135, 4050-600 Porto, Portugal
5  Laboratory for Integrative and Translational Research in Population Health (ITR), Porto, Portugal
6  Environmental Health Department, INSA, Rua Alexandre Herculano 321, 4000-053 Porto, Portugal
7  Universidade da Coruña, Grupo DICOMOSA, Centro Interdisciplinar de Química e Bioloxía - CICA, Departamento de Psicología, Facultad de Ciencias de la Educación, Campus Elviña s/n, 15071, A Coruña, Spain
Academic Editor: José Luis Arias Mediano

Abstract:

Cerium dioxide nanoparticles (CeO2NP) show antioxidant enzyme-mimetic properties and ROS scavenging activity, making them a promising material for nanomedicine, although their potential adverse effects are not totally understood yet. The objective of this work was to assess the biological behaviour of CeO2NP in human neuronal SH-SY5Y and glial A172 cells. After carrying out the physical-chemical characterization of the CeO2NP and analysing their ability to be taken up by neuronal and glial cells, the possible alterations in cell viability and the induction of DNA double strand breaks was determined in the presence of these NP by means of MTT assay and γH2AX assay, respectively. The possible existence of interference of the NP with the assay methodologies was previously addressed and corrected when necessary. The results obtained showed that, even though there was a significant dose- and time-dependent internalization of the NP by both cell lines, the CeO2NP generally presented scarce cyto- or genotoxicity, essentially depending on the NP exposure time and being restricted to higher doses. These results provide a better understanding of CeO2NP interaction with cellular systems and their possible adverse effects, specifically at the level of the nervous system. These data may be used in risk assessment of exposure to these NP, and as a basis for establishing good practice guidelines for their management, in addition to contributing to increase the knowledge about the impact of CeO2NP on human health.

Funding: Ministry of Science and Innovation: MCIN/AEI/10.13039/501100011033 (Grant PID2020-114908GA-I00), Xunta de Galicia (ED431B 2022/16), CICA-Disrupting Project 2021SEM‐B2, Ministry of Education, Culture and Sport [BEAGAL18/00142 to V.V.], and FCT [SFRH/BPD/122112/2016 to A.T.R]. This communication is based upon work from COST Action "Nano2Clinic" CA17140, supported by COST (European Cooperation in Science and Technology).

Keywords: Cerium dioxide nanoparticles; cytotoxicity; genotoxicity; neuronal cells; glial cells
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