Evidence map›Paper›PMID 40203036›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Substrate stress relaxation regulates monolayer fluidity and leader cell formation for collectively migrating epithelia.

Frank Charbonier, Junqin Zhu, Raleigh Slyman, Cole Allan, Ovijit Chaudhuri

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Traction Force Microscopy for Viscoelastic Substrates: A Semi-Analytical Method.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Substrate stress relaxation regulates monolayer fluidity and leader cell formation for collectively migrating epithelia.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Frank Charbonier *Department of Mechanical Engineering, Stanford University, Stanford, CA 94305.ORCID 0000-0002-0367-6327
Junqin Zhu *Department of Biology, Stanford University, Stanford, CA 94305.ORCID 0000-0002-8159-6402
Raleigh SlymanDepartment of Mechanical Engineering, Stanford University, Stanford, CA 94305.
Cole AllanDepartment of Mechanical Engineering, Stanford University, Stanford, CA 94305.
Ovijit ChaudhuriDepartment of Mechanical Engineering, Stanford University, Stanford, CA 94305.ORCID 0000-0002-9287-3401

Funding

Role of extracellular matrix malleability in mediating breast cancer cell invasion and migrationR37CA214136 · NCI · STANFORD UNIVERSITY · PI CHAUDHURI, OVIJIT · 2018 to 2024
$2.5M
Regulation of Adherent Cell Proliferation by Matrix ViscoelasticityR01GM148535 · NIGMS · STANFORD UNIVERSITY · PI Ovijit Chaudhuri · 2023 to 2026
$1.5M
NCI NIH HHS R37 CA214136NIGMS NIH HHS R01 GM148535NSF (NSF) CMMI 1846367NSF | NSF Graduate Research Fellowship Program (GRFP) DGE-1656518)
6 · The paper itself

Abstract

Collective migration of epithelial tissues is a critical feature of developmental morphogenesis and tissue homeostasis. Coherent motion of cell collectives requires large-scale coordination of motion and force generation and is influenced by mechanical properties of the underlying substrate. While tissue viscoelasticity is a ubiquitous feature of biological tissues, its role in mediating collective cell migration is unclear. Here, we have investigated the impact of substrate stress relaxation on the migration of micropatterned epithelial monolayers. Epithelial monolayers exhibit faster collective migration on viscoelastic alginate substrates with slower relaxation timescales, which are more elastic, relative to substrates with faster stress relaxation, which exhibit more viscous loss. Faster migration on slow-relaxing substrates is associated with reduced substrate deformation, greater monolayer fluidity, and enhanced leader cell formation. In contrast, monolayers on fast-relaxing substrates generate substantial substrate deformations and are more jammed within the bulk, with reduced formation of transient lamellipodial protrusions past the monolayer edge leading to slower overall expansion. This work reveals features of collective epithelial dynamics on soft, viscoelastic materials and adds to our understanding of cell-substrate interactions at the tissue scale.

Indexed as

Cell MovementEpithelial CellsAlginatesAnimalsDogsElasticityEpitheliumMadin Darby Canine Kidney CellsStress, MechanicalViscosityAlginatescell–substrate interactionscollective cell migrationmechanotransductiontissue mechanicsviscoelastic substrates

Identifiers

PMID40203036
PMCPMC12012536

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.