Successful micronucleus testing with the EPI/001 3D reconstructed epidermis model: Preliminary findings

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• 作者：E. Andres^a ; ^{ericandres@natura.net} ; J. Molinari^a ; N. Remoué ; ^a ; V.M. Sá ; -Rocha^b ; C. Barrichello^a ; S.P. Hurtado^b
• 关键词：RHE ; reconstructed human epidermis ; MMC ; mitomycin C ; VB ; vinblastine ; MGG ; May&ndash ; Grü ; nwald&ndash ; Giemsa ; H&E ; Haematoxylin & Eosin ; MN ; micronucleus
• 刊名：Mutation Research/Genetic Toxicology and Environmental Mutagenesis
• 出版年：2012
• 期刊代码：31_13835718
• 类别：pha
• 出版时间：18 March, 2012
• 卷：743
• 期：1-2
• 页码：36-41
• 文件大小：477 K

摘要

Currently, the cosmetics industry relies on the results of in vitro genotoxicity tests to assess the safety of chemicals. Although the cytokinesis-block micronucleus (CBMN) test for the detection of cells that have divided once is routinely used and currently accepted by regulatory agencies, it has some limitations. Reconstituted human epidermis (RHE) is widely used in safety assessments because its physiological properties resemble those of the skin, and because it allows testing of substances such as hydrophobic compounds. Thus, the micronucleus test is being adapted for application in RHE-reconstructed tissues.

Here we investigated whether two different reconstructed epidermis models (EPI/001 from Straticell, and RHE/S/17 from Skinethic) are suitable for application of the micronucleus test. We found that acetone does not modify micronucleus frequency, cell viability, and model structure, compared with non-treated RHE. Treatment of the EPI/001 model with mitomycin C and vinblastine resulted in a dose-dependent increase of micronucleus frequency as well as a decrease of tissue viability and of binucleated cell rate, while no changes of the epidermal structure were observed. The number of binucleated cells obtained with the RHE/S/17 model was too small to permit micronucleus testing. These results indicate that the proliferative rate of the tissue used is a critical parameter in performing the micronucleus test on a 3D model.