Evidence map›Paper›PMID 27512142›Full record

ArticleOpen biology2016

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

Tong Chen, Blanca Gomez-Escoda, Javier Munoz-Garcia, Julien Babic, Laurent Griscom, Pei-Yun Jenny Wu, Damien Coudreuse

Abstract read
In one paragraph

Article in Open biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Tong ChenSyntheCell team, Institute of Genetics and Development, CNRS UMR 6290, 2 avenue du Pr. Léon Bernard, 35043 Rennes, France.
Blanca Gomez-EscodaGenome Duplication and Maintenance team, Institute of Genetics and Development, CNRS UMR 6290, 2 avenue du Pr. Léon Bernard, 35043 Rennes, France.
Javier Munoz-GarciaSyntheCell team, Institute of Genetics and Development, CNRS UMR 6290, 2 avenue du Pr. Léon Bernard, 35043 Rennes, France.
Julien BabicSyntheCell team, Institute of Genetics and Development, CNRS UMR 6290, 2 avenue du Pr. Léon Bernard, 35043 Rennes, France.
Laurent GriscomSyntheCell team, Institute of Genetics and Development, CNRS UMR 6290, 2 avenue du Pr. Léon Bernard, 35043 Rennes, France.
Pei-Yun Jenny WuGenome Duplication and Maintenance team, Institute of Genetics and Development, CNRS UMR 6290, 2 avenue du Pr. Léon Bernard, 35043 Rennes, France pei-yun.wu@univ-rennes1.fr.
Damien CoudreuseSyntheCell team, Institute of Genetics and Development, CNRS UMR 6290, 2 avenue du Pr. Léon Bernard, 35043 Rennes, France damien.coudreuse@univ-rennes1.fr.ORCID 0000-0003-2534-1621

Funding

European Research Council 310849Worldwide Cancer Research 11-0685
6 · The paper itself

Abstract

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.

Indexed as

Equipment DesignHeLa CellsHumansMicrofluidicsReproducibility of ResultsTemperatureYeastscell biologycontrol of cellular environmentlive-cell imagingmicrofluidicsmicroscopy

Identifiers

PMID27512142
PMCPMC5008015

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.