Graduate Program in Genetics, Department of Genetics, Federal University of Paraná (UFPR).
Safety of Product Department, Grupo Boticário.
J Vis Exp. 2023 Jan 6(191). doi: 10.3791/64860.
Fish cell lines have become increasingly used in ecotoxicity studies, and cytotoxicity assays have been proposed as methods to predict fish acute toxicity. Thus, this protocol presents cytotoxicity assays modified to evaluate cell viability in zebrafish (Danio rerio) embryo (ZEM2S) and liver (ZFL) cell lines in 96-well plates. The cytotoxicity endpoints evaluated are mitochondrial integrity (Alamar Blue [AB] and MTT assays), membrane integrity via esterase activity (CFDA-AM assay), and lysosomal membrane integrity (Neutral Red [NR] assay). After the exposure of the test substances in a 96-well plate, the cytotoxicity assays are performed; here, AB and CFDA-AM are carried out simultaneously, followed by NR on the same plate, while the MTT assay is performed on a separate plate. The readouts for these assays are taken by fluorescence for AB and CFDA-AM, and absorbance for MTT and NR. The cytotoxicity assays performed with these fish cell lines can be used to study the acute toxicity of chemical substances on fish.
鱼类细胞系在生态毒性研究中得到了越来越广泛的应用,细胞毒性测定已被提议作为预测鱼类急性毒性的方法。因此,本方案提出了在 96 孔板中评估斑马鱼胚胎(ZEM2S)和肝脏(ZFL)细胞系细胞活力的细胞毒性测定方法的修改。评估的细胞毒性终点包括线粒体完整性(Alamar Blue [AB] 和 MTT 测定)、通过酯酶活性评估的膜完整性(CFDA-AM 测定)和溶酶体膜完整性(中性红 [NR] 测定)。在 96 孔板中暴露测试物质后,进行细胞毒性测定;在这里,AB 和 CFDA-AM 同时进行,然后在同一块板上进行 NR,而 MTT 测定则在另一块板上进行。这些测定的读数通过 AB 和 CFDA-AM 的荧光,以及 MTT 和 NR 的吸光度来获得。使用这些鱼类细胞系进行的细胞毒性测定可用于研究化学物质对鱼类的急性毒性。