High-throughput automated organoid culture via stem-cell aggregation in microcavity arrays

被引:281
作者
Brandenberg, Nathalie [1 ,7 ]
Hoehnel, Sylke [1 ,7 ]
Kuttler, Fabien [2 ]
Homicsko, Krisztian [3 ,4 ]
Ceroni, Camilla [1 ,7 ]
Ringel, Till [5 ]
Gjorevski, Nikolce [1 ,8 ]
Schwank, Gerald [5 ]
Coukos, George [3 ,4 ]
Turcatti, Gerardo [2 ]
Lutolf, Matthias P. [1 ,6 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Bioengn, Lab Stem Cell Bioengn, Sch Life Sci, Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Sch Life Sci, Biomol Screening Facil, Lausanne, Switzerland
[3] Univ Lausanne, Univ Hosp Lausanne, Dept Oncol, Lausanne, Switzerland
[4] Univ Lausanne, Lausanne Branch, Ludwig Inst Canc Res, Lausanne, Switzerland
[5] Swiss Fed Inst Technol, HPL, Inst Mol Hlth Sci, Zurich, Switzerland
[6] Ecole Polytech Fed Lausanne, Sch Basic Sci, Inst Chem Sci & Engn, Lausanne, Switzerland
[7] Startlab SUN Biosci, Batiment SE-B, Epalignes, Switzerland
[8] Roche Pharma Res & Early Dev, Basel, Switzerland
关键词
IN-VITRO; MODEL;
D O I
10.1038/s41551-020-0565-2
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Thousands of individual gastrointestinal organoids cultured on microcavity arrays without a solid extracellular matrix allow for high-throughput drug screening and for high-content image-based phenotypic analyses. Stem-cell-derived epithelial organoids are routinely used for the biological and biomedical modelling of tissues. However, the complexity, lack of standardization and quality control of stem cell culture in solid extracellular matrices hampers the routine use of the organoids at the industrial scale. Here, we report the fabrication of microengineered cell culture devices and scalable and automated methods for suspension culture and real-time analysis of thousands of individual gastrointestinal organoids trapped in microcavity arrays within a polymer-hydrogel substrate. The absence of a solid matrix substantially reduces organoid heterogeneity, which we show for mouse and human gastrointestinal organoids. We use the devices to screen for anticancer drug candidates with patient-derived colorectal cancer organoids, and apply high-content image-based phenotypic analyses to reveal insights into mechanisms of drug action. The scalable organoid-culture technology should facilitate the use of organoids in drug development and diagnostics.
引用
收藏
页码:863 / +
页数:15
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