Evidence map›Paper›PMID 31607653›Full record

ArticleDevelopmental cell2019

Membrane Tension Orchestrates Rear Retraction in Matrix-Directed Cell Migration.

Joseph H R Hetmanski, Henry de Belly, Ignacio Busnelli, Thomas Waring, Roshna V Nair, Vanesa Sokleva, Oana Dobre, Angus Cameron, Nils Gauthier, Christophe Lamaze and 8 more

Abstract read
In one paragraph

Article in Developmental cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing 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

89 citing papers in PubMed.

  1. Article
  2. Caveolae mechanics in cellular functions and disease.Nature reviews. Molecular cell biology · 2026
    Review
  3. Bleb expansion requires transient membrane invaginations that sequester curvature-preferring proteins.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  19. Review
  20. Review

29 more citing papers are in PubMed but not listed here.

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

18 authors.

Joseph H R HetmanskiWellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK.
Henry de BellyMRC Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK; Institute for the Physics of Living Systems, University College London, London WC1E 6BT, UK.
Ignacio BusnelliINSERM UMR_S1109, Tumor Biomechanics, Strasbourg 67200, France; Université de Strasbourg, Strasbourg 67000, France; Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg 67000, France.
Thomas WaringInstitute of Translational Medicine, Cellular and Molecular Physiology, University of Liverpool, Liverpool L69 3BX, UK.
Roshna V NairINM, Leibniz Institute for New Materials, Campus D226, 66123 Saarbrücken, Germany.
Vanesa SoklevaWellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK.
Oana DobreWellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK.
Angus CameronBarts Cancer Institute, Queen Mary University of London, London EC1M 6BQ, UK.
Nils GauthierIFOM, the FIRC Institute for Molecular Oncology, Milan 20139, Italy.
Christophe LamazeInstitut Curie - Centre de Recherche, PSL Research University, CNRS UMR 3666, INSERM U1143, Membrane Dynamics and Mechanics of Intracellular Signaling Laboratory, 75248 Paris Cedex 05, France.
Joe SwiftWellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK.
Aránzazu Del CampoUniversité de Strasbourg, Strasbourg 67000, France.
Tobias StarborgWellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK.
Tobias ZechInstitute of Translational Medicine, Cellular and Molecular Physiology, University of Liverpool, Liverpool L69 3BX, UK.
Jacky G GoetzINSERM UMR_S1109, Tumor Biomechanics, Strasbourg 67200, France; Université de Strasbourg, Strasbourg 67000, France; Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg 67000, France.
Ewa K PaluchMRC Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK; Institute for the Physics of Living Systems, University College London, London WC1E 6BT, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, UK.
Jean-Marc SchwartzWellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK.
Patrick T CaswellWellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK. Electronic address: patrick.caswell@manchester.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/L024551/1Medical Research Council MR/M009114/1Medical Research Council MR/R009376/1Medical Research Council MR/S008632/1Wellcome TrustWellcome Trust 203128/Z/16/Z
6 · The paper itself

Abstract

In development, wound healing, and cancer metastasis, vertebrate cells move through 3D interstitial matrix, responding to chemical and physical guidance cues. Protrusion at the cell front has been extensively studied, but the retraction phase of the migration cycle is not well understood. Here, we show that fast-moving cells guided by matrix cues establish positive feedback control of rear retraction by sensing membrane tension. We reveal a mechanism of rear retraction in 3D matrix and durotaxis controlled by caveolae, which form in response to low membrane tension at the cell rear. Caveolae activate RhoA-ROCK1/PKN2 signaling via the RhoA guanidine nucleotide exchange factor (GEF) Ect2 to control local F-actin organization and contractility in this subcellular region and promote translocation of the cell rear. A positive feedback loop between cytoskeletal signaling and membrane tension leads to rapid retraction to complete the migration cycle in fast-moving cells, providing directional memory to drive persistent cell migration in complex matrices.

Indexed as

Actin CytoskeletonActinsAnimalsCaveolaeCell Line, TumorCell MembraneCell MovementCell PolarityCell Surface ExtensionsCytoskeletonCytosolExtracellular MatrixHumansMiceProtein Kinase CPseudopodiaActinsProtein Kinase Cprotein kinase NrhoA GTP-Binding ProteinRHOA protein, humanrho-Associated KinasesROCK1 protein, humancaveolaecell invasioncell migrationcytoskeletondurotaxisextracellular matrixmembrane tensionRhoGTPase

Identifiers

PMID31607653
PMCPMC6863396

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Registered trials

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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.