Evidence map›Paper›PMID 31400917›Full record

ArticleBiophysical journal2019

A Biophysical Model for Curvature-Guided Cell Migration.

Maxime Vassaux, Laurent Pieuchot, Karine Anselme, Maxence Bigerelle, Jean-Louis Milan

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 40 citations in OpenAlex.

  1. The role of geometry in morphogenesis.Development (Cambridge, England) · 2026
    Review
  2. Guiding of Cell Migration over Sloped Steps Using TiOJournal of functional biomaterials · 2026
    Article
  3. Article
  4. Review
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  8. A minimal physical model for curvotaxis driven by curved protein complexes at the cell's leading edge.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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 at 1 institution in 1 country.

Maxime VassauxAix Marseille Univ, CNRS, ISM, Marseille, France; Department of Orthopaedics and Traumatology, Institute for Locomotion, APHM, Sainte-Marguerite Hospital, Marseille, France. Electronic address: m.vassaux@ucl.ac.uk.
Laurent PieuchotUniversité de Haute-Alsace, CNRS, IS2M, UMR 7361, Mulhouse, France; Université de Strasbourg, Strasbourg, France. Electronic address: laurent.pieuchot@uha.fr.
Karine AnselmeUniversité de Haute-Alsace, CNRS, IS2M, UMR 7361, Mulhouse, France; Université de Strasbourg, Strasbourg, France.
Maxence BigerelleUniversité de Valenciennes et du Hainaut Cambrésis, Laboratoire d'Automatique, de Mécanique et d'Informatique industrielle et Humaine (LAMIH), UMR-CNRS 8201, Le Mont Houy, Valenciennes, France.
Jean-Louis MilanAix Marseille Univ, CNRS, ISM, Marseille, France; Department of Orthopaedics and Traumatology, Institute for Locomotion, APHM, Sainte-Marguerite Hospital, Marseille, France.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The latest experiments have shown that adherent cells can migrate according to cell-scale curvature variations via a process called curvotaxis. Despite identification of key cellular factors, a clear understanding of the mechanism is lacking. We employ a mechanical model featuring a detailed description of the cytoskeleton filament networks, the viscous cytosol, the cell adhesion dynamics, and the nucleus. We simulate cell adhesion and migration on sinusoidal substrates. We show that cell adhesion on three-dimensional curvatures induces a gradient of pressure inside the cell that triggers the internal motion of the nucleus. We propose that the resulting out-of-equilibrium position of the nucleus alters cell migration directionality, leading to cell motility toward concave regions of the substrate, resulting in lower potential energy states. Altogether, we propose a simple mechanism explaining how intracellular mechanics enable the cells to react to substratum curvature, induce a deterministic cell polarization, and break down cells basic persistent random walk, which correlates with latest experimental evidences.

Indexed as

Biophysical PhenomenaCell MovementCell ShapeModels, BiologicalCell NucleusCell Size

Identifiers

PMID31400917
PMCPMC6818171
OpenAlexW2963848519

What OpenQuestion holds

Textmetadata
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.