Rohwedder A, Knipp S, Esteves F O, Hale M, Ketchen S E, Treanor D, Brüning-Richardson A
Light Laboratories, School of Molecular and Cellular Biology, Faculty of Biological Sciences University of Leeds, Leeds, UK.
School of Applied Sciences, University of Huddersfield, Huddersfield, UK.
Interface Focus. 2022 Aug 12;12(5):20220016. doi: 10.1098/rsfs.2022.0016. eCollection 2022 Oct 6.
Three-dimensional (3D) spheroid cultures are generating increasing interest in cancer research, e.g. for the evaluation of pharmacological effects of novel small molecule inhibitors. This is mainly due to the fact that such 3D structures reflect physiological characteristics of tumours and the cellular microenvironments they reside in more faithfully than two-dimensional (2D) cell cultures; in addition, they allow the reduction of animal experiments while providing significantly relevant human-based models. Quantification of such organoid structures as well as the mainly slice-based acquisition and thus forced 2D representation of 3D spheroids provide a challenge for the interpretation of the associated generated data. Here, we provide a novel open-source workflow to reconstruct a 3D entity from slice-recorded microscopical images with or without treatment with anti-migratory small molecule inhibitors. This reconstruction produces distinct point clouds as basis for subsequent comparison of basic readout parameters using average computer processor, memory and graphics resources within an acceptable time frame. We were able to validate the usefulness of this workflow using 3D data generated by various imaging techniques, including -stacks from confocal microscopy and histochemically labelled spheroid sectioning, and demonstrate the possibility to accurately characterize inhibitor effects in great detail.
三维(3D)球体培养在癌症研究中越来越受到关注,例如用于评估新型小分子抑制剂的药理作用。这主要是因为这种3D结构比二维(2D)细胞培养更忠实地反映了肿瘤及其所处细胞微环境的生理特征;此外,它们在减少动物实验的同时提供了显著相关的基于人类的模型。对这种类器官结构的量化以及主要基于切片的采集,从而对3D球体进行强制二维表示,给相关生成数据的解释带来了挑战。在这里,我们提供了一种新颖的开源工作流程,用于从切片记录的显微镜图像重建3D实体,无论是否用抗迁移小分子抑制剂处理。这种重建产生独特的点云,作为后续在可接受的时间框架内使用普通计算机处理器、内存和图形资源比较基本读出参数的基础。我们能够使用各种成像技术生成的3D数据验证该工作流程的有用性,包括共聚焦显微镜的z-stack和组织化学标记的球体切片,并证明了详细准确地表征抑制剂作用的可能性。