Multiscale cytometry and regulation of 3D cell cultures on a chip
Sébastien Sart,
Raphaël F.-X. Tomasi,
Gabriel Amselem and
Charles N. Baroud ()
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Sébastien Sart: Ecole Polytechnique, CNRS-UMR7646
Raphaël F.-X. Tomasi: Ecole Polytechnique, CNRS-UMR7646
Gabriel Amselem: Ecole Polytechnique, CNRS-UMR7646
Charles N. Baroud: Ecole Polytechnique, CNRS-UMR7646
Nature Communications, 2017, vol. 8, issue 1, 1-13
Abstract:
Abstract 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.
Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00475-x
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DOI: 10.1038/s41467-017-00475-x
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