Graduate Program in Genetics, Department of Genetics, Federal University of Paraná (UFPR), Paraná, Brazil.
Grupo Boticário, R&D Department, São José dos Pinhais, Paraná, Brazil.
Ecotoxicology. 2021 Nov;30(9):1893-1909. doi: 10.1007/s10646-021-02459-6. Epub 2021 Aug 11.
Fish cell spheroids are promising 3D culture models for vertebrate replacement in ecotoxicology. However, new alternative ecotoxicological methods must be adapted for applications in industry and for regulatory purposes; such methods must be cost-effective, simple to manipulate and provide rapid results. Therefore, we compared the effectiveness of the traditional hanging drop (HD), orbital shaking (OS), and HD combined with OS (HD+OS) methods on the formation of zebrafish cell line spheroids (ZFL and ZEM2S). Time in HD (3-5 days) and different 96-well plates [flat-bottom or ultra-low attachment of round-bottom (ULA-plates)] in OS were evaluated. Easy handling, rapid spheroid formation, uniform-sized spheroids, and circularity were assessed to identify the best spheroid protocol. Traditional HD alone did not result in ZFL spheroid formation, whereas HD (5 days)+OS did. When using the OS, spheroids only formed on the ULA-plate. Both HD+OS and OS were reproducible in size (177.50 ± 2.81 µm and 225.62 ± 19.20 µm, respectively) and circularity (0.83 ± 0.02 and 0.80 ± 0.01, respectively) of ZFL spheroids. Nevertheless, HD+OS required a considerable time to completely form spheroids (10 days) and intensive handling, whereas the OS was fast (5 days of incubation) and simple. OS also yielded reproducible ZEM2S spheroids in 1 day (226.23 ± 0.57 µm diameter and 0.80 ± 0.01 circularity). In conclusion, OS in ULA-plate is an effective and simple spheroid protocol for high-throughput ecotoxicity testing. This study contributes to identify a fast, reproducible, and simple protocol of single piscine spheroid formation in 96-well plates and supports the application of fish 3D model in industry and academia.
鱼类细胞球体是替代脊椎动物进行生态毒理学研究的有前途的 3D 培养模型。然而,新的替代生态毒理学方法必须适应工业和监管目的的应用;这些方法必须具有成本效益,易于操作,并能提供快速结果。因此,我们比较了传统的悬滴(HD)、轨道摇晃(OS)和 HD 与 OS 结合(HD+OS)方法在斑马鱼细胞系球体(ZFL 和 ZEM2S)形成中的效果。评估了 HD 中的时间(3-5 天)和 OS 中的不同 96 孔板[平底或圆底超低附着(ULA 板)]。为了确定最佳球体方案,评估了操作的简便性、球体的快速形成、球体的均匀大小和球体的圆度。单独的传统 HD 不能使 ZFL 形成球体,而 HD(5 天)+OS 可以。在使用 OS 时,只有在 ULA 板上才能形成球体。HD+OS 和 OS 在 ZFL 球体的大小(分别为 177.50±2.81μm 和 225.62±19.20μm)和圆度(分别为 0.83±0.02 和 0.80±0.01)方面均具有重现性。然而,HD+OS 完全形成球体(10 天)需要相当多的时间和密集的操作,而 OS 则非常快速(孵育 5 天)且简单。OS 还能在 1 天内产生重现性好的 ZEM2S 球体(直径 226.23±0.57μm,圆度 0.80±0.01)。总之,ULA 板中的 OS 是一种有效的、简单的高通量生态毒性测试球体方案。本研究有助于确定一种快速、可重现和简单的方案,用于在 96 孔板中形成单个鱼类球体,并支持鱼类 3D 模型在工业和学术界的应用。