Evidence map›Paper›PMID 28687667›Full record

ArticleThe Journal of cell biology2017

Membrane tension controls adhesion positioning at the leading edge of cells.

Bruno Pontes, Pascale Monzo, Laurent Gole, Anabel-Lise Le Roux, Anita Joanna Kosmalska, Zhi Yang Tam, Weiwei Luo, Sophie Kan, Virgile Viasnoff, Pere Roca-Cusachs and 2 more

Abstract readVideo-Audio Media
In one paragraph

Article in The Journal of cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing 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

65 citing papers in PubMed.

  1. Mechanical forces stimulate Golgi export.The Journal of cell biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Myosin 2 - A general contractor for the cytoskeleton.Current opinion in cell biology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Transient inhibition of meniscus cell migration following acute inflammatory challenge.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  20. Article

5 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

12 authors.

Bruno PontesMechanobiology Institute, National University of Singapore, Singapore.
Pascale MonzoMechanobiology Institute, National University of Singapore, Singapore.ORCID 0000-0002-0081-3701
Laurent GoleMechanobiology Institute, National University of Singapore, Singapore.
Anabel-Lise Le RouxInstitute for Bioengineering of Catalonia, The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID 0000-0003-4152-5658
Anita Joanna KosmalskaInstitute for Bioengineering of Catalonia, The Barcelona Institute of Science and Technology, Barcelona, Spain.
Zhi Yang TamMechanobiology Institute, National University of Singapore, Singapore.
Weiwei LuoMechanobiology Institute, National University of Singapore, Singapore.
Sophie KanMechanobiology Institute, National University of Singapore, Singapore.
Virgile ViasnoffMechanobiology Institute, National University of Singapore, Singapore.
Pere Roca-CusachsInstitute for Bioengineering of Catalonia, The Barcelona Institute of Science and Technology, Barcelona, Spain.
Lisa Tucker-KelloggMechanobiology Institute, National University of Singapore, Singapore.
Nils C GauthierMechanobiology Institute, National University of Singapore, Singapore nils.gauthier@ifom.eu.ORCID 0000-0003-1260-3477

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell migration is dependent on adhesion dynamics and actin cytoskeleton remodeling at the leading edge. These events may be physically constrained by the plasma membrane. Here, we show that the mechanical signal produced by an increase in plasma membrane tension triggers the positioning of new rows of adhesions at the leading edge. During protrusion, as membrane tension increases, velocity slows, and the lamellipodium buckles upward in a myosin II-independent manner. The buckling occurs between the front of the lamellipodium, where nascent adhesions are positioned in rows, and the base of the lamellipodium, where a vinculin-dependent clutch couples actin to previously positioned adhesions. As membrane tension decreases, protrusion resumes and buckling disappears, until the next cycle. We propose that the mechanical signal of membrane tension exerts upstream control in mechanotransduction by periodically compressing and relaxing the lamellipodium, leading to the positioning of adhesions at the leading edge of cells.

Indexed as

Cell AdhesionCell MovementMechanotransduction, CellularActinsAnimalsCell Adhesion MoleculesCell MembraneCells, CulturedCell ShapeComputer SimulationCytoskeletonFibroblastsMiceMicrofilament ProteinsMicroscopy, FluorescenceMicroscopy, VideoActinsCell Adhesion MoleculesMicrofilament ProteinsMyosin Type IIPhosphoproteinsVasodilator-Stimulated PhosphoproteinVinculin

Identifiers

PMID28687667
PMCPMC5584154

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.