Tateno Chise, Fukumuro Masahito, Masumori Shoji, Kakuni Masakazu, Ishida Yuji, Shimada Takashi, Hayashi Makoto
PhoenixBio Co., Ltd., 3-4-1, Kagamiyama, Higashi-Hiroshima, 739-0046, Japan.
BioSafety Research Center, Inc., 582-2, Shio Shinden, Iwata, 437-1213, Japan.
Mutat Res Genet Toxicol Environ Mutagen. 2019 Mar;839:9-12. doi: 10.1016/j.mrgentox.2019.01.003. Epub 2019 Jan 14.
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.
遗传毒性试验的特点是有方法、体外或体内靶标以及终点。许多细胞类型都被用作靶标,包括细菌细胞、培养的哺乳动物细胞和体内的啮齿动物细胞。人类细胞是评估与接触化学物质相关的人类风险的最重要靶标。几乎无一例外,遗传毒性试验中使用的人类细胞都是培养细胞。在此,我们在PXB小鼠(肝脏已被人类肝细胞重新填充的嵌合小鼠)中测试了人类肝细胞,将其作为体内遗传毒性试验的靶细胞来源。我们应用单细胞凝胶电泳(彗星)试验来检测DNA损伤,并应用微核试验来评估染色体畸变。这些嵌合小鼠可作为遗传毒性试验的宝贵模型系统。