Micronuclei detection by flow cytometry as a high-throughput approach for the genotoxicity testing of nanomaterials

Thousands of nanomaterials (NMs)-containing products are currently under development or incorporated in the consumer market, despite our very limited understanding of their genotoxic potential. Taking into account that the toxicity and genotoxicity of NMs strongly depend on their physicochemical cha...

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Detalles Bibliográficos
Autores: García Rodríguez, Alba|||0000-0002-1175-7418, Kazantseva, Liliya, Vila Vecilla, Laura|||0000-0001-5573-4886, Rubio Lorente, Laura|||0000-0002-2088-3803, Velázquez Henar, Antonia|||0000-0003-3254-4312, Ramírez de Haro, Ma. José|||0000-0003-1417-7731, Marcos Dauder, Ricardo|||0000-0001-7891-357X, Hernández Bonilla, Alba|||0000-0001-6938-1233
Tipo de recurso: artículo
Fecha de publicación:2019
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:216823
Acceso en línea:https://ddd.uab.cat/record/216823
https://dx.doi.org/urn:doi:10.3390/nano9121677
Access Level:acceso abierto
Palabra clave:BEAS-2B cells
Flow cytometry MN (FCMN) assay
TiO2NPs
ZnONPs
CeO2NPs
AgNPs
MWCNTs
Descripción
Sumario:Thousands of nanomaterials (NMs)-containing products are currently under development or incorporated in the consumer market, despite our very limited understanding of their genotoxic potential. Taking into account that the toxicity and genotoxicity of NMs strongly depend on their physicochemical characteristics, many variables must be considered in the safety evaluation of each given NM. In this scenario, the challenge is to establish high-throughput methodologies able to generate rapid and robust genotoxicity data that can be used to critically assess and/or predict the biological effects associated with those NMs being under development or already present in the market. In this study, we have evaluated the advantages of using a flow cytometry-based approach testing micronucleus (MNs) induction (FCMN assay). In the frame of the EU NANoREG project, we have tested six different NMs-namely NM100 and NM101 (TiO2NPs), NM110 (ZnONPs), NM212 (CeO2NPs), NM300K (AgNPs) and NM401 (multi-walled carbon nanotubes (MWCNTs)). The obtained results confirm the ability of AgNPs and MWCNTs to induce MN in the human bronchial epithelial BEAS-2B cell line, whereas the other tested NMs retrieved non-significant increases in the MN frequency. Based on the alignment of the results with the data reported in the literature and the performance of the FCMN assay, we strongly recommend this assay as a reference method to systematically evaluate the potential genotoxicity of NMs.