Multiscale cytometry and regulation of 3D cell cultures on a chip

被引:118
作者
Sart, Sebastien [1 ]
Tomasi, Raphael F. -X. [1 ]
Amselem, Gabriel [1 ]
Baroud, Charles N. [1 ]
机构
[1] Ecole Polytech, Dept Mech, Lab Hydrodynam LadHyX, CNRS,UMR7646, F-91128 Palaiseau, France
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
基金
欧洲研究理事会;
关键词
DROPLET MICROFLUIDICS; MULTICELLULAR SPHEROIDS; HEPATOCYTE SPHEROIDS; ENDOTHELIAL-CELLS; MOUSE HEPATOCYTES; TUMOR SPHEROIDS; LIVER-CELLS; E-CADHERIN; IN-VITRO; METABOLISM;
D O I
10.1038/s41467-017-00475-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Three-dimensional cell culture is emerging as a more relevant alternative to the traditional two-dimensional format. Yet the ability to perform cytometry at the single cell level on intact three-dimensional spheroids or together with temporal regulation of the cell microenvironment remains limited. Here we describe a microfluidic platform to perform high-density three-dimensional culture, controlled stimulation, and observation in a single chip. The method extends the capabilities of droplet microfluidics for performing long-term culture of adherent cells. Using arrays of 500 spheroids per chip, in situ immunocytochemistry and image analysis provide multiscale cytometry that we demonstrate at the population scale, on 104 single spheroids, and over 105 single cells, correlating functionality with cellular location within the spheroids. Also, an individual spheroid can be extracted for further analysis or culturing. This will enable a shift towards quantitative studies on three-dimensional cultures, under dynamic conditions, with implications for stem cells, organs-on-chips, or cancer research.
引用
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页数:13
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