Dayeh Vivian R, Bols Niels C, Tanneberger Katrin, Schirmer Kristin, Lee Lucy E J
Department of Biology, University of Waterloo, Waterloo, Ontario, Canada.
Curr Protoc Toxicol. 2013 May;Chapter 1:Unit1.5. doi: 10.1002/0471140856.tx0105s56.
Protocols for evaluating chemical toxicity at the cellular level using fish cell lines are described in this unit. Routine methodologies for growing salmonid cell lines, and using them in aquatic toxicology studies that support the mandate of the Organization for Economic Co-operation and Development (OECD) to reduce the use of whole animals in toxicity testing, are presented. Rapid, simple, cost-effective tests evaluating viability of cells with three indicator dyes per sample provides a broad overview of the sensitivity of cells to chemical contaminants. This fluorometric assay involves: (1) alamar blue for metabolic activity, (2) CFDA-AM for membrane integrity, and (3) neutral red for lysosomal function. These protocols are conveniently performed in semi-unison within the same multiwell plates and read at three different wavelengths. Detailed step-by-step descriptions of the assays, parameters to consider, troubleshooting, and guidelines for data interpretation are provided as essential tools for investigating environmental aquatic contaminants at the cellular level.
本单元介绍了使用鱼类细胞系在细胞水平评估化学毒性的方案。文中介绍了培养鲑鱼细胞系的常规方法,以及将其用于水生毒理学研究的方法,这些研究支持经济合作与发展组织(OECD)减少在毒性测试中使用整体动物的任务要求。使用三种指示染料对每个样品的细胞活力进行快速、简单且经济高效的测试,可全面了解细胞对化学污染物的敏感性。这种荧光测定法包括:(1)用于代谢活性的alamar蓝,(2)用于膜完整性的CFDA-AM,以及(3)用于溶酶体功能的中性红。这些方案可在同一多孔板中方便地半同步进行,并在三个不同波长下读取数据。文中提供了测定法的详细分步说明、需考虑的参数、故障排除方法以及数据解释指南,作为在细胞水平研究环境水生污染物的重要工具。