Evidence map›Paper›PMID 39787053›Full record

ArticlePLoS computational biology2025

Fast yet force-effective mode of supracellular collective cell migration due to extracellular force transmission.

Amrit Bagchi, Bapi Sarker, Jialiang Zhang, Marcus Foston, Amit Pathak

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Amrit BagchiDepartment of Mechanical Engineering & Materials Science, Washington University, St. Louis, Missouri, United States of America.ORCID 0000-0002-4145-6763
Bapi SarkerDepartment of Mechanical Engineering & Materials Science, Washington University, St. Louis, Missouri, United States of America.
Jialiang ZhangDepartment of Energy, Environmental & Chemical Engineering, Washington University, St. Louis, Missouri, United States of America.ORCID 0000-0002-7421-8024
Marcus FostonDepartment of Energy, Environmental & Chemical Engineering, Washington University, St. Louis, Missouri, United States of America.
Amit PathakDepartment of Mechanical Engineering & Materials Science, Washington University, St. Louis, Missouri, United States of America.ORCID 0000-0003-4006-5119

Funding

Epithelial Cell Mechanobiology in Mechanically Heterogeneous MicroenvironmentsR35GM128764 · NIGMS · WASHINGTON UNIVERSITY · PI PATHAK, AMIT · 2018 to 2022
$2.2M
NIGMS NIH HHS R35 GM128764
6 · The paper itself

Abstract

Cell collectives, like other motile entities, generate and use forces to move forward. Here, we ask whether environmental configurations alter this proportional force-speed relationship, since aligned extracellular matrix fibers are known to cause directed migration. We show that aligned fibers serve as active conduits for spatial propagation of cellular mechanotransduction through matrix exoskeleton, leading to efficient directed collective cell migration. Epithelial (MCF10A) cell clusters adhered to soft substrates with aligned collagen fibers (AF) migrate faster with much lesser traction forces, compared to random fibers (RF). Fiber alignment causes higher motility waves and transmission of normal stresses deeper into cell monolayer while minimizing shear stresses and increased cell-division based fluidization. By contrast, fiber randomization induces cellular jamming due to breakage in motility waves, disrupted transmission of normal stresses, and heightened shear driven flow. Using a novel motor-clutch model, we explain that such 'force-effective' fast migration phenotype occurs due to rapid stabilization of contractile forces at the migrating front, enabled by higher frictional forces arising from simultaneous compressive loading of parallel fiber-substrate connections. We also model 'haptotaxis' to show that increasing ligand connectivity (but not continuity) increases migration efficiency. According to our model, increased rate of front stabilization via higher resistance to substrate deformation is sufficient to capture 'durotaxis'. Thus, our findings reveal a new paradigm wherein the rate of leading-edge stabilization determines the efficiency of supracellular collective cell migration.

Indexed as

Cell MovementExtracellular MatrixMechanotransduction, CellularModels, BiologicalBiomechanical PhenomenaCollagenComputational BiologyHumansStress, MechanicalCollagen

Identifiers

PMID39787053
PMCPMC11717197

What OpenQuestion holds

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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.