Evidence map›Paper›PMID 27373558›Full record

ArticleScientific reports2016

On-Chip Quantitative Measurement of Mechanical Stresses During Cell Migration with Emulsion Droplets.

D Molino, S Quignard, C Gruget, F Pincet, Y Chen, M Piel, J Fattaccioli

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Review
  3. Measurement of adhesion and traction of cells at high yield reveals an energetic ratchet operating during nephron condensation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Review
  5. Article
  6. Quantifying local stiffness and forces in soft biological tissues using droplet optical microcavities.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Article
  8. Article
  9. A roadmap for translational cancer glycoimmunology at single cell resolution.Journal of experimental & clinical cancer research : CR · 2022
    Review
  10. Article
  11. Oncoimmunology Meets Organs-on-Chip.Frontiers in molecular biosciences · 2021
    Review
  12. Article
  13. Article
  14. Review
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.

D MolinoÉcole Normale Supérieure - PSL Research University, Département de Chimie, 24 rue Lhomond, F-75005 Paris, France.
S QuignardÉcole Normale Supérieure - PSL Research University, Département de Chimie, 24 rue Lhomond, F-75005 Paris, France.
C GrugetLaboratoire de Physique Statistique, Ecole Normale Supérieure, Université Pierre et Marie Curie, Université Paris Diderot, Centre National de la Recherche Scientifique UMR8550, 24 rue Lhomond, Paris 75005, France.
F PincetLaboratoire de Physique Statistique, Ecole Normale Supérieure, Université Pierre et Marie Curie, Université Paris Diderot, Centre National de la Recherche Scientifique UMR8550, 24 rue Lhomond, Paris 75005, France.
Y ChenÉcole Normale Supérieure - PSL Research University, Département de Chimie, 24 rue Lhomond, F-75005 Paris, France.
M PielInstitut Curie, CNRS UMR 144, 26 rue d'Ulm, 75005, Paris, France.
J FattaccioliÉcole Normale Supérieure - PSL Research University, Département de Chimie, 24 rue Lhomond, F-75005 Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability of immune cells to migrate within narrow and crowded spaces is a critical feature involved in various physiological processes from immune response to metastasis. Several in-vitro techniques have been developed so far to study the behaviour of migrating cells, the most recent being based on the fabrication of microchannels within which cells move. To address the question of the mechanical stress a cell is able to produce during the encounter of an obstacle while migrating, we developed a hybrid microchip made of parallel PDMS channels in which oil droplets are sparsely distributed and serve as deformable obstacles. We thus show that cells strongly deform droplets while passing them. Then, we show that the microdevice can be used to study the influence of drugs on migration at the population level. Finally, we describe a quantitative analysis method of the droplet deformation that allows measuring in real-time the mechanical stress exerted by a single cell. The method presented herein thus constitutes a powerful analytical tool for cell migration studies under confinement.

Indexed as

Cell MovementLab-On-A-Chip DevicesStress, MechanicalAmidesEmulsionsHL-60 CellsHumansNumerical Analysis, Computer-AssistedPyridinesSurface TensionTime-Lapse ImagingAmidesEmulsionsPyridinesY 27632

Identifiers

PMID27373558
PMCPMC4931467

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Registered trials

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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.