Evidence map›Paper›PMID 20100912›Full record

ArticleThe Journal of cell biology2010

Force transmission in migrating cells.

Maxime F Fournier, Roger Sauser, Davide Ambrosi, Jean-Jacques Meister, Alexander B Verkhovsky

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
9.2field-weighted citation impact, top 1% of its field
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

114 citing papers in PubMed, 234 citations in OpenAlex.

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  13. Friction patterns guide actin network contraction.Proceedings of the National Academy of Sciences of the United States of America · 2023
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54 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 2 countries.

Maxime F FournierLaboratoire de Biophysique Cellulaire, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland. maxime.fournier@epfl.ch
Roger Sauser
Davide Ambrosi
Jean-Jacques Meister
Alexander B Verkhovsky
École Polytechnique Fédérale de Lausanne · CHPolitecnico di Milano · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During cell migration, forces generated by the actin cytoskeleton are transmitted through adhesion complexes to the substrate. To investigate the mechanism of force generation and transmission, we analyzed the relationship between actin network velocity and traction forces at the substrate in a model system of persistently migrating fish epidermal keratocytes. Front and lateral sides of the cell exhibited much stronger coupling between actin motion and traction forces than the trailing cell body. Further analysis of the traction-velocity relationship suggested that the force transmission mechanisms were different in different cell regions: at the front, traction was generated by a gripping of the actin network to the substrate, whereas at the sides and back, it was produced by the network's slipping over the substrate. Treatment with inhibitors of the actin-myosin system demonstrated that the cell body translocation could be powered by either of the two different processes, actomyosin contraction or actin assembly, with the former associated with significantly larger traction forces than the latter.

Indexed as

Stress, MechanicalActin CytoskeletonAnimalsBiomechanical PhenomenaCell AdhesionCell MovementCell PolarityCells, CulturedCell ShapeCytochalasin DCytoskeletonFishesHeterocyclic Compounds, 4 or More RingsKeratinocytesModels, BiologicalMyosinsblebbistatinCytochalasin DHeterocyclic Compounds, 4 or More RingsMyosinsProtein Synthesis Inhibitors

Identifiers

PMID20100912
PMCPMC2812525
OpenAlexW2107750328

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

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.