| Literature DB >> 30744813 |
Chise Tateno1, Masahito Fukumuro2, Shoji Masumori2, Masakazu Kakuni3, Yuji Ishida3, Takashi Shimada3, Makoto Hayashi4.
Abstract
Genotoxicity assays are characterized by a method, an in vitro or in vivo target, and an endpoint. Many cell types have been used as targets, including bacterial cells, cultured mammalian cells, and rodent cells in vivo. Human cells are the most important target for evaluating the risk to humans associated with exposure to chemicals. Almost exclusively, the human cells used in genotoxicity tests have been cultured cells. Here, we have tested human hepatocytes in PXB-mice®, chimeric mice in which the liver has been repopulated with human hepatocytes, as a source of target cells for in vivo genotoxicity assays. We applied the single-cell gel electrophoresis (comet) assay to detect DNA damage and the micronucleus assay to evaluate chromosomal aberrations. These chimeric mice can serve as a valuable model system for genotoxicity assays.Entities:
Keywords: AFB1; Comet assay; ENU; In vivo; Liver micronucleus assay
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Year: 2019 PMID: 30744813 DOI: 10.1016/j.mrgentox.2019.01.003
Source DB: PubMed Journal: Mutat Res Genet Toxicol Environ Mutagen ISSN: 1383-5718 Impact factor: 2.873