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A high-throughput three-dimensional cell migration assay for toxicity screening with mobile device-based macroscopic image analysis

机译:用于基于移动设备的宏观图像分析进行毒性筛选的高通量三维细胞迁移测定

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摘要

There is a growing demand for in vitro assays for toxicity screening in three-dimensional (3D)environments. In this study, 3D cell culture using magnetic levitation was used to create an assay in whichcells were patterned into 3D rings that close over time. The rate of closure was determined from time-lapseimages taken with a mobile device and related to drug concentration. Rings of human embryonic kidneycells (HEK293) and tracheal smooth muscle cells (SMCs) were tested with ibuprofen and sodium dodecylsulfate (SDS). Ring closure correlated with the viability and migration of cells in two dimensions (2D).Images taken using a mobile device were similar in analysis to images taken with a microscope. Ring closuremay serve as a promising label-free and quantitative assay for high-throughput in vivo toxicity in 3Dcultures.
机译:对于在三维(3D)环境中进行毒性筛查的体外测定法,存在越来越高的需求。在这项研究中,使用磁悬浮的3D细胞培养被用于创建一种检测方法,其中将细胞图案化为随时间关闭的3D环。根据移动设备拍摄的延时图像确定闭合率,并与药物浓度相关。用布洛芬和十二烷基硫酸钠(SDS)测试了人类胚胎肾细胞(HEK293)和气管平滑肌细胞(SMC)的环。闭环与二维细胞的活力和迁移有关(2D)。使用移动设备拍摄的图像在分析中与使用显微镜拍摄的图像相似。闭环可以作为3D培养物中高通量体内毒性的有希望的无标记和定量测定方法。

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