Evidence map›Paper›PMID 30273354›Full record

ArticlePLoS computational biology2018

Cooperation of dual modes of cell motility promotes epithelial stress relaxation to accelerate wound healing.

Michael F Staddon, Dapeng Bi, A Pasha Tabatabai, Visar Ajeti, Michael P Murrell, Shiladitya Banerjee

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Physical models of embryonic epithelial healing.PLoS computational biology · 2026
    Review
  3. Article
  4. Article
  5. Confinement induces internal flows in adherent cell aggregates.Journal of the Royal Society, Interface · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Mechanosensory feedback loops during chronic inflammation.Frontiers in cell and developmental biology · 2023
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Hindbrain neuropore tissue geometry determines asymmetric cell-mediated closure dynamics in mouse embryos.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Article
  18. Junctional and cytoplasmic contributions in wound healing.Journal of the Royal Society, Interface · 2020
    Article
  19. Article
  20. Polarity during tissue repair, a multiscale problem.Current opinion in cell biology · 2020
    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

6 authors at 3 institutions in 2 countries.

Michael F StaddonDepartment of Physics and Astronomy, University College London, London, United Kingdom.ORCID 0000-0002-8240-7554
Dapeng BiDepartment of Physics, Northeastern University, Boston, Massachusetts, United States of America.ORCID 0000-0003-4850-8666
A Pasha TabatabaiDepartment of Biomedical Engineering, Yale University, New Haven, Connecticut, United States of America.
Visar AjetiDepartment of Biomedical Engineering, Yale University, New Haven, Connecticut, United States of America.
Michael P MurrellDepartment of Biomedical Engineering, Yale University, New Haven, Connecticut, United States of America.
Shiladitya BanerjeeDepartment of Physics and Astronomy, University College London, London, United Kingdom.ORCID 0000-0001-8000-2556
Yale University · USUniversity College London · GBNortheastern University · US

Funding

Systems analysis of phenotypic switch in control of cancer invasionU54CA209992 · NCI · YALE UNIVERSITY · PI LEVCHENKO, ANDRE · 2016 to 2021
$10.1M
NCI NIH HHS U54 CA209992
6 · The paper itself

Abstract

Collective cell migration in cohesive units is vital for tissue morphogenesis, wound repair, and immune response. While the fundamental driving forces for collective cell motion stem from contractile and protrusive activities of individual cells, it remains unknown how their balance is optimized to maintain tissue cohesiveness and the fluidity for motion. Here we present a cell-based computational model for collective cell migration during wound healing that incorporates mechanochemical coupling of cell motion and adhesion kinetics with stochastic transformation of active motility forces. We show that a balance of protrusive motility and actomyosin contractility is optimized for accelerating the rate of wound repair, which is robust to variations in cell and substrate mechanical properties. This balance underlies rapid collective cell motion during wound healing, resulting from a tradeoff between tension mediated collective cell guidance and active stress relaxation in the tissue.

Indexed as

AnimalsCell MovementComputational BiologyDogsElastic ModulusEpithelial CellsFocal AdhesionsMadin Darby Canine Kidney CellsModels, BiologicalWound Healing

Identifiers

PMID30273354
PMCPMC6181425
OpenAlexW2886451184

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.