A Rohwedder, S Knipp, F O Esteves, M Hale, S E Ketchen, D Treanor, A Brüning-Richardson
{"title":"'Cloudbuster': a Python-based open source application for three-dimensional reconstruction and quantification of stacked biological imaging samples.","authors":"A Rohwedder, S Knipp, F O Esteves, M Hale, S E Ketchen, D Treanor, A Brüning-Richardson","doi":"10.1098/rsfs.2022.0016","DOIUrl":null,"url":null,"abstract":"<p><p>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 <i>z</i>-stacks from confocal microscopy and histochemically labelled spheroid sectioning, and demonstrate the possibility to accurately characterize inhibitor effects in great detail.</p>","PeriodicalId":13795,"journal":{"name":"Interface Focus","volume":"12 5","pages":"20220016"},"PeriodicalIF":3.6000,"publicationDate":"2022-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372645/pdf/rsfs.2022.0016.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Interface Focus","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1098/rsfs.2022.0016","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/10/6 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
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 z-stacks from confocal microscopy and histochemically labelled spheroid sectioning, and demonstrate the possibility to accurately characterize inhibitor effects in great detail.
三维(3D)球形培养物在癌症研究(如评估新型小分子抑制剂的药理作用)中正引起越来越多的兴趣。这主要是因为这种三维结构比二维(2D)细胞培养物更忠实地反映了肿瘤的生理特征及其所处的细胞微环境;此外,它们还能减少动物实验,同时提供与人类密切相关的模型。此类类器官结构的定量以及主要基于切片的采集和三维球体的强制二维表示为相关生成数据的解释带来了挑战。在此,我们提供了一种新颖的开源工作流程,可在使用或不使用抗迁移小分子抑制剂的情况下,从切片记录的显微图像中重建三维实体。在可接受的时间范围内,利用一般的计算机处理器、内存和图形资源,这种重建方法可产生独特的点云,作为随后比较基本读出参数的基础。我们利用各种成像技术生成的三维数据(包括共聚焦显微镜的 Z 叠片和组织化学标记的球状切片)验证了这一工作流程的实用性,并证明了精确描述抑制剂效应细节的可能性。
期刊介绍:
Each Interface Focus themed issue is devoted to a particular subject at the interface of the physical and life sciences. Formed of high-quality articles, they aim to facilitate cross-disciplinary research across this traditional divide by acting as a forum accessible to all. Topics may be newly emerging areas of research or dynamic aspects of more established fields. Organisers of each Interface Focus are strongly encouraged to contextualise the journal within their chosen subject.