Das Viswanath, Fürst Tomáš, Gurská Soňa, Džubák Petr, Hajdúch Marián
Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.
Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic
J Biomol Screen. 2016 Oct;21(9):923-30. doi: 10.1177/1087057116651867. Epub 2016 May 25.
Spheroid cultures of cancer cells reproduce the spatial dimension-induced in vivo tumor traits more effectively than the conventional two-dimensional cell cultures. With growing interest in spheroids for high-throughput screening (HTS) assays, there is an increasing demand for cost-effective miniaturization of reproducible spheroids in microtiter plates (MPs). However, well-to-well variability in spheroid size, shape, and growth is a frequently encountered problem with almost every culture method that has prevented the transfer of spheroids to the HTS platform. This variability partly arises due to increased susceptibility of MPs to edge effects and evaporation-induced changes in the growth of spheroids. In this study, we examined the effect of evaporation on the reproducibility of spheroids of tumor and nontumor cell lines in 384-well plates, and show that culture conditions that prevent evaporation-induced medium loss result in the formation of uniform spheroids across the plate. Additionally, we also present a few technical improvements to increase the scalability of the liquid-overlay spheroid culturing technique in MPs, together with a simple software routine for the quantification of spheroid size. We believe that these cost-effective improvements will aid in further improvement of spheroid cultures for HTS drug discovery.
与传统的二维细胞培养相比,癌细胞的球体培养能更有效地重现空间维度诱导的体内肿瘤特征。随着人们对用于高通量筛选(HTS)分析的球体的兴趣日益浓厚,对在微孔板(MPs)中实现可重复球体的经济高效小型化的需求也在增加。然而,球体大小、形状和生长的孔间变异性是几乎每种培养方法都经常遇到的问题,这阻碍了球体向HTS平台的转移。这种变异性部分是由于MPs对边缘效应的敏感性增加以及蒸发引起的球体生长变化所致。在本研究中,我们研究了蒸发对384孔板中肿瘤和非肿瘤细胞系球体重现性的影响,并表明防止蒸发引起的培养基损失的培养条件会导致整个平板形成均匀的球体。此外,我们还提出了一些技术改进措施,以提高MPs中液体覆盖球体培养技术的可扩展性,以及一个用于定量球体大小的简单软件程序。我们相信,这些经济高效的改进将有助于进一步改进用于HTS药物发现的球体培养。