Evidence map›Paper›PMID 39468334›Full record

ArticleNature materials2024

Rupture strength of living cell monolayers.

Julia Duque, Alessandra Bonfanti, Jonathan Fouchard, Lucia Baldauf, Sara R Azenha, Emma Ferber, Andrew Harris, Elias H Barriga, Alexandre J Kabla, Guillaume Charras

Abstract read
In one paragraph

Article in Nature materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Extracellular matrix chemistry tunes bacterial biofilm metabolism and optimizes fitness.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Article
  11. Article
  12. Shape, Strain, and Stability: Epithelia Under High Strain.bioRxiv : the preprint server for biology · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Cellular mechanisms of traumatic brain injury.npj biological physics and mechanics · 2025
    Review
  20. 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

10 authors.

Julia DuqueLondon Centre for Nanotechnology, University College London, London, UK. j.duque@ucl.ac.uk.ORCID 0000-0003-2805-5313
Alessandra BonfantiDepartment of Civil and Environmental Engineering, Politecnico di Milano, Milan, Italy.
Jonathan FouchardLondon Centre for Nanotechnology, University College London, London, UK.ORCID 0000-0002-9976-462X
Lucia BaldaufLondon Centre for Nanotechnology, University College London, London, UK.ORCID 0000-0001-5200-4044
Sara R AzenhaGulbenkian Institute of Science (IGC), Oeiras, Portugal.ORCID 0000-0003-2044-3768
Emma FerberLondon Centre for Nanotechnology, University College London, London, UK.
Andrew HarrisMechanical and Aerospace Engineering, Carleton University, Ottawa, Ontario, Canada.
Elias H BarrigaGulbenkian Institute of Science (IGC), Oeiras, Portugal.ORCID 0000-0003-2912-3613
Alexandre J KablaDepartment of Engineering, University of Cambridge, Cambridge, UK. ajk61@cam.ac.uk.ORCID 0000-0002-0280-3531
Guillaume CharrasLondon Centre for Nanotechnology, University College London, London, UK. g.charras@ucl.ac.uk.ORCID 0000-0002-7902-0279

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To fulfil their function, epithelial tissues need to sustain mechanical stresses and avoid rupture. Although rupture is usually undesired, it is central to some developmental processes, for example, blastocoel formation. Nonetheless, little is known about tissue rupture because it is a multiscale phenomenon that necessitates comprehension of the interplay between mechanical forces and biological processes at the molecular and cellular scales. Here we characterize rupture in epithelial monolayers using mechanical measurements, live imaging and computational modelling. We show that despite consisting of only a single layer of cells, monolayers can withstand surprisingly large deformations, often accommodating several-fold increases in their length before rupture. At large deformation, epithelia increase their stiffness multiple fold in a process controlled by a supracellular network of keratin filaments. Perturbing the keratin network organization fragilized the monolayers and prevented strain-stiffening. Although the kinetics of adhesive bond rupture ultimately control tissue strength, tissue rheology and the history of deformation set the strain and stress at the onset of fracture.

Indexed as

Stress, MechanicalAnimalsBiomechanical PhenomenaDogsEpithelial CellsKeratinsMadin Darby Canine Kidney CellsModels, BiologicalKeratins

Identifiers

PMID39468334
PMCPMC11525174

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.