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Recommendations, evaluation and validation of a semi-automated, fluorescent-based scoring protocol for micronucleus testing in human cells

Seager, Anna L.; Br�sehafer, Katja; Chapman, Katherine E.; Scott, Andrew D.; Doherty, Ann T.; Doak, Shareen H.; Johnson, George E.; Jenkins, Gareth J.S.; Thomas, Adam; Shah, Ume Kulsoom; Wills, John; Manshian, Bella

Authors

Anna L. Seager

Katja Br�sehafer

Katherine E. Chapman

Andrew D. Scott

Ann T. Doherty

Shareen H. Doak

George E. Johnson

Gareth J.S. Jenkins

Adam Thomas Adam7.Thomas@uwe.ac.uk
Senior Lecturer in Human Genetics and Genomics

Ume Kulsoom Shah

John Wills

Bella Manshian



Abstract

Micronucleus (MN) induction is an established cytogenetic end point for evaluating structural and numerical chromosomal alterations in genotoxicity testing. A semi-automated scoring protocol for the assessment of MN preparations from human cell lines and a 3D skin cell model has been developed and validated. Following exposure to a range of test agents, slides were stained with 4-6-diamidino-2-phenylindole (DAPI) and scanned by use of the MicroNuc module of metafer 4, after the development of a modified classifier for selecting MN in binucleate cells. A common difficulty observed with automated systems is an artefactual output of high false positives, in the case of the metafer system this is mainly due to the loss of cytoplasmic boundaries during slide preparation. Slide quality is paramount to obtain accurate results. We show here that to avoid elevated artefactual-positive MN outputs, diffuse cell density and low-intensity nuclear staining are critical. Comparisons between visual (Giemsa stained) and automated (DAPI stained) MN frequencies and dose-response curves were highly correlated (R2 = 0.70 for hydrogen peroxide, R2 = 0.98 for menadione, R2 = 0.99 for mitomycin C, R2 = 0.89 for potassium bromate and R2 = 0.68 for quantum dots), indicating the system is adequate to produce biologically relevant and reliable results. Metafer offers many advantages over conventional scoring including increased output and statistical power, and reduced scoring subjectivity, labour and costs. Further, the metafer system is easily adaptable for use with a range of different cells, both suspension and adherent human cell lines. Awareness of the points raised here reduces the automatic positive errors flagged and drastically reduces slide scoring time, making metafer an ideal candidate for genotoxic biomonitoring and population studies and regulatory genotoxic testing. © The Author 2014.

Citation

Jenkins, G. J., Johnson, G. E., Doak, S. H., Doherty, A. T., Scott, A. D., Chapman, K. E., …Thomas, A. (2014). Recommendations, evaluation and validation of a semi-automated, fluorescent-based scoring protocol for micronucleus testing in human cells. Mutagenesis, 29(3), 155-164. https://doi.org/10.1093/mutage/geu008

Journal Article Type Article
Acceptance Date Apr 4, 2014
Online Publication Date Apr 4, 2014
Publication Date Jan 1, 2014
Deposit Date Jul 2, 2019
Journal Mutagenesis
Print ISSN 0267-8357
Electronic ISSN 1464-3804
Publisher Oxford University Press (OUP)
Peer Reviewed Peer Reviewed
Volume 29
Issue 3
Pages 155-164
DOI https://doi.org/10.1093/mutage/geu008
Public URL https://uwe-repository.worktribe.com/output/1467292
Publisher URL https://doi.org/10.1093/mutage/geu008