Evidence map›Paper›PMID 42661757›Full record

ArticleCommunications physics2026

Partial fluidization theory of collective cell migration.

Igor S Aranson, Lev S Tsimring

Abstract read
In one paragraph

Article in Communications physics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Igor S AransonDepartments of Biomedical Engineering, Chemistry, and Mathematics, Pennsylvania State University, University Park, PA USA.ORCID 0000-0002-4062-5393
Lev S TsimringSynthetic Biology Institute, Department of Bioengineering, University of California, San Diego, La Jolla, CA USA.ORCID 0000-0003-0709-3548

Funding

Engineered Gene Circuits for Basic Science and BiotechnologyR01GM069811 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HASTY, JEFF M, TSIMRING, LEV S · 2004 to 2025
$13.6M
NIGMS NIH HHS R01 GM069811
6 · The paper itself

Abstract

Collective cell and tissue migration is crucial for various biological processes, including morphogenesis, wound healing, and cancer metastasis. Migrating cell monolayers often exhibit complex viscoelastic responses and coexistence of solid and liquid-like behaviors that are not well understood in the framework of existing theories. Here, we introduce a partial fluidization approach for collective cell migration. We treat the cell monolayer as a single albeit spatially and temporally non-uniform phase bridging two distinct states: a viscous liquid and a soft solid with an elastic response to shear. The continuous transition between these states is controlled by the fluidization order parameter that, in turn, depends on the normalized shear stress. The model successfully captures key experimental observations: solid-like plug flow of cells in a microfluidic channel, spatial coexistence of moving and immobile domains in cell monolayers, and solid body-like rotational flow of cells in a circular chamber. The approach provides insights into the physical mechanisms of cell migration. It can be extended to more realistic situations, such as confluent monolayers on curved, compliant, or degradable surfaces as well as three-dimensional proliferating tissues and chemical signaling.

Indexed as

Cellular motilityFluids

Identifiers

PMID42661757
PMCPMC13518239

What OpenQuestion holds

Textmetadata
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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.