A drug-compatible and temperature controlled microfluidic device for live-cell imaging

被引:19
作者
Chen, Tong [1 ]
Gomez-Escoda, Blanca [2 ]
Munoz-Garcia, Javier [1 ]
Babic, Julien [1 ]
Griscom, Laurent [1 ]
Wu, Pei-Yun Jenny [2 ]
Coudreuse, Damien [1 ]
机构
[1] CNRS UMR 6290, Inst Genet & Dev, SyntheCell Team, 2 Ave Pr Leon Bernard, F-35043 Rennes, France
[2] CNRS UMR 6290, Inst Genet & Dev, Genome Duplicat & Maintenance Team, 2 Ave Pr Leon Bernard, F-35043 Rennes, France
基金
欧洲研究理事会;
关键词
live-cell imaging; cell biology; microfluidics; control of cellular environment; microscopy; YEAST SCHIZOSACCHAROMYCES-POMBE; FISSION YEAST; SMALL MOLECULES; F-ACTIN; ABSORPTION; POLY(DIMETHYLSILOXANE); CHIPS; CYCLE; DNA; FABRICATION;
D O I
10.1098/rsob.160156
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Monitoring cellular responses to changes in growth conditions and perturbation of targeted pathways is integral to the investigation of biological processes. However, manipulating cells and their environment during live-cell-imaging experiments still represents a major challenge. While the coupling of microfluidics with microscopy has emerged as a powerful solution to this problem, this approach remains severely underexploited. Indeed, most microdevices rely on the polymer polydimethylsiloxane (PDMS), which strongly absorbs a variety of molecules commonly used in cell biology. This effect of the microsystems on the cellular environment hampers our capacity to accurately modulate the composition of the medium and the concentration of specific compounds within the microchips, with implications for the reliability of these experiments. To overcome this critical issue, we developed new PDMS-free microdevices dedicated to live-cell imaging that show no interference with small molecules. They also integrate a module for maintaining precise sample temperature both above and below ambient as well as for rapid temperature shifts. Importantly, changes in medium composition and temperature can be efficiently achieved within the chips while recording cell behaviour by microscopy. Compatible with different model systems, our platforms provide a versatile solution for the dynamic regulation of the cellular environment during live-cell imaging.
引用
收藏
页数:14
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