类有机物
干细胞
高通量筛选
药品
药物发现
吞吐量
计算生物学
计算机科学
生物
细胞生物学
药理学
生物信息学
操作系统
无线
作者
Xiaomeng Li,Guoxiang Fu,Long Zhang,Ruo‐Yu Guan,Peiyuan Tang,Jialing Zhang,Xinxin Rao,Shengzhi Chen,Xiaoya Xu,Yi Zhou,Yun Deng,Tao� Lv,Xingfeng He,Shaobo Mo,Peiyuan Mu,Jianjun Gao,Guoqiang Hua
标识
DOI:10.1186/s13287-022-02902-3
摘要
Organoids are three-dimensional structures that closely recapitulate tissue architecture and cellular composition, thereby holding great promise for organoid-based drug screening. Although growing in three-dimensional provides the possibility for organoids to recapitulate main features of corresponding tissues, it makes it incommodious for imaging organoids in two-dimensional and identifying surviving organoids from surrounding dead cells after organoids being treated by irradiation or chemotherapy. Therefore, significant work remains to establish high-quality controls to standardize organoid analyses and make organoid models more reproducible.In this study, the Z-stack imaging technique was used for the imaging of three-dimensional organoids to gather all the organoids' maximum cross sections in one imaging. The combination of live cell staining fluorescent dye Calcein-AM and ImageJ assessment was used to analyze the survival of organoids treated by irradiation or chemotherapy.We have established a novel quantitative high-throughput imaging assay that harnesses the scalability of organoid cultures. Using this assay, we can capture organoid growth over time, measure multiple whole-well organoid readouts, and show the different responses to drug treatments.In summary, combining the Z-stack imaging technique and fluorescent labeling methods, we established an assay for the imaging and analysis of three-dimensional organoids. Our data demonstrated the feasibility of using organoid-based platforms for high-throughput drug screening assays.
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