A novel micronucleus in vitro assay utilizing human hematopoietic stem cells

•An alternative in vitro micronucleus test based on human cells has been developed according to the 3Rs principle.•A model of ex vivo culture of human erythrocytes has been applied to test genotoxicity in vitro.•The developed test shows a high screening potential for genotoxicity testing in human pr...

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Veröffentlicht in:Toxicology in vitro 2015-10, Vol.29 (7), p.1897-1905
Hauptverfasser: Kotova, N., Hebert, N., Härnwall, E.-L., Vare, D., Mazurier, C., Douay, L., Jenssen, D., Grawé, J.
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Sprache:eng
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Zusammenfassung:•An alternative in vitro micronucleus test based on human cells has been developed according to the 3Rs principle.•A model of ex vivo culture of human erythrocytes has been applied to test genotoxicity in vitro.•The developed test shows a high screening potential for genotoxicity testing in human primary cell cultures. The induction of micronucleated reticulocytes in the bone marrow is a sensitive indicator of chromosomal damage. Therefore, the micronucleus assay in rodents is widely used in genotoxicity and carcinogenicity testing. A test system based on cultured human primary cells could potentially provide better prediction compared to animal tests, increasing patient safety while also implementing the 3Rs principle, i.e. replace, reduce and refine. Hereby, we describe the development of an in vitro micronucleus assay based on animal-free ex vivo culture of human red blood cells from hematopoietic stem cells. To validate the method, five clastogens with direct action, three clastogens requiring metabolic activation, four aneugenic and three non-genotoxic compounds have been tested. Also, different metabolic systems have been applied. Flow cytometry was used for detection and enumeration of micronuclei. Altogether, the results were in agreement with the published data and indicated that a sensitive and cost effective in vitro assay to assess genotoxicity with a potential to high-throughput screening has been developed.
ISSN:0887-2333
1879-3177
1879-3177
DOI:10.1016/j.tiv.2015.07.018