Evidence map›Paper›PMID 41387450›Full record

ArticleNature communications2025

Spatiotemporal coupling of caveolae mechanosensing and RhoA-GEFs regulates cell polarity and directional migration.

Vibha Singh, Victor Breton, Christine Viaris de Lesegno, Anne-Sophie Macé, Philippe Bun, Cédric M Blouin, Amit Singh Vishen, Pierre Sens, Christophe Lamaze

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Caveolae mechanics in cellular functions and disease.Nature reviews. Molecular cell biology · 2026
    Review
  3. Article
  4. 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

9 authors.

Vibha SinghInstitut Curie-Centre de Recherche, PSL Research University, Membrane Mechanics and Dynamics of Intracellular Signaling Laboratory, Paris, France.ORCID http://orcid.org/0000-0002-1280-6920
Victor BretonInstitut Curie-Centre de Recherche, PSL Research University, Membrane Mechanics and Dynamics of Intracellular Signaling Laboratory, Paris, France.ORCID http://orcid.org/0000-0003-4433-5665
Christine Viaris de LesegnoInstitut Curie-Centre de Recherche, PSL Research University, Membrane Mechanics and Dynamics of Intracellular Signaling Laboratory, Paris, France.
Anne-Sophie MacéCell and Tissue Imaging Facility (PICT-IBiSA), Institut Curie, PSL Research University, Paris, France.
Philippe BunInstitute of Psychiatry and Neuroscience of Paris (IPNP), Membrane Traffic in Healthy and Diseased Brain Laboratory, Université Paris Cité, Université Paris Cité, Paris, France.ORCID http://orcid.org/0000-0002-7975-1768
Cédric M BlouinInstitut Curie-Centre de Recherche, PSL Research University, Membrane Mechanics and Dynamics of Intracellular Signaling Laboratory, Paris, France.ORCID http://orcid.org/0000-0003-0800-0948
Amit Singh VishenLaboratoire Physics of Cells and Cancer, Institut Curie, PSL Research University, Sorbonne Université (CNRS UMR168), Sorbonne Université, Paris, France.
Pierre SensLaboratoire Physics of Cells and Cancer, Institut Curie, PSL Research University, Sorbonne Université (CNRS UMR168), Sorbonne Université, Paris, France. pierre.sens@curie.fr.ORCID http://orcid.org/0000-0003-4523-3791
Christophe LamazeInstitut Curie-Centre de Recherche, PSL Research University, Membrane Mechanics and Dynamics of Intracellular Signaling Laboratory, Paris, France. christophe.lamaze@curie.fr.ORCID http://orcid.org/0000-0001-5430-2707

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Migrating cells dynamically adapt their morphogenetic programs in response to microenvironmental changes, requiring coordinated spatiotemporal integration of mechanical and biochemical signals. The plasma membrane, through membrane tension and actin dynamics modulation, is essential for cell motility. Caveolae, small plasma membrane invaginations, act as mechanosensors to buffer tension changes under mechanical stress. Recent evidence suggests a role for caveolae in cell migration. Here, we demonstrate that breast cancer cells exhibit a front-rear asymmetry in caveolae and caveolin-1 scaffolds, which is regulated by membrane tension and is crucial for persistent migration and cell directionality. RhoA-driven cell contraction relies on the spatiotemporally coordinated assembly of caveolae and recruitment of RhoA-GEFs at the cell rear. These results are supported by a physical model establishing a feedback loop between local membrane tension and contractility, through caveolae formation and disruption. Our findings underscore the importance of caveolae mechanosensing in regulating RhoA activation and guiding cell migration.

Indexed as

CaveolaeCell MovementCell PolarityMechanotransduction, CellularrhoA GTP-Binding ProteinCaveolin 1Cell Line, TumorCell MembraneFemaleHumansCaveolin 1rhoA GTP-Binding ProteinRHOA protein, human

Identifiers

PMID41387450
PMCPMC12796338

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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.