Evidence map›Paper›PMID 39394209›Full record

ArticleNature communications2024

N-cadherin crosstalk with integrin weakens the molecular clutch in response to surface viscosity.

Eva Barcelona-Estaje, Mariana A G Oliva, Finlay Cunniffe, Aleixandre Rodrigo-Navarro, Paul Genever, Matthew J Dalby, Pere Roca-Cusachs, Marco Cantini, Manuel Salmeron-Sanchez

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  11. Review
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  14. Article
  15. Environmental Toxicants and Their Disruption of Integrin Signaling in Lipid Rafts.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
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.

Eva Barcelona-EstajeCentre for the Cellular Microenvironment, Advanced Research Centre, University of Glasgow, Glasgow, UK.ORCID 0009-0008-7308-5806
Mariana A G OlivaCentre for the Cellular Microenvironment, Advanced Research Centre, University of Glasgow, Glasgow, UK.ORCID 0000-0002-3195-067X
Finlay CunniffeCentre for the Cellular Microenvironment, Advanced Research Centre, University of Glasgow, Glasgow, UK.
Aleixandre Rodrigo-NavarroCentre for the Cellular Microenvironment, Advanced Research Centre, University of Glasgow, Glasgow, UK.ORCID 0000-0002-3786-0464
Paul GeneverDepartment of Biology, University of York, York, UK.
Matthew J DalbyCentre for the Cellular Microenvironment, Advanced Research Centre, University of Glasgow, Glasgow, UK.ORCID 0000-0002-0528-3359
Pere Roca-CusachsInstitute for Bioengineering of Catalonia (IBEC), the Barcelona Institute of Technology (BIST), Barcelona, Spain. proca@ibecbarcelona.eu.ORCID 0000-0001-6947-961X
Marco CantiniCentre for the Cellular Microenvironment, Advanced Research Centre, University of Glasgow, Glasgow, UK. Marco.Cantini@glasgow.ac.uk.ORCID 0000-0003-0326-1508
Manuel Salmeron-SanchezCentre for the Cellular Microenvironment, Advanced Research Centre, University of Glasgow, Glasgow, UK. Manuel.Salmeron-Sanchez@glasgow.ac.uk.ORCID 0000-0002-8112-2100

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 101054728EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 874889Medical Research Council MR/S005412/1RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/X033554/1RCUK | MRC | Medical Research Foundation MR/S005412/1Royal Society RGS/R1/231400
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) interact with their surroundings via integrins, which link to the actin cytoskeleton and translate physical cues into biochemical signals through mechanotransduction. N-cadherins enable cell-cell communication and are also linked to the cytoskeleton. This crosstalk between integrins and cadherins modulates MSC mechanotransduction and fate. Here we show the role of this crosstalk in the mechanosensing of viscosity using supported lipid bilayers as substrates of varying viscosity. We functionalize these lipid bilayers with adhesion peptides for integrins (RGD) and N-cadherins (HAVDI), to demonstrate that integrins and cadherins compete for the actin cytoskeleton, leading to an altered MSC mechanosensing response. This response is characterised by a weaker integrin adhesion to the environment when cadherin ligation occurs. We model this competition via a modified molecular clutch model, which drives the integrin/cadherin crosstalk in response to surface viscosity, ultimately controlling MSC lineage commitment.

Indexed as

CadherinsIntegrinsMesenchymal Stem CellsActin CytoskeletonAnimalsCell AdhesionCell CommunicationHumansLipid BilayersMechanotransduction, CellularOligopeptidesViscosityarginyl-glycyl-aspartic acidCadherinsIntegrinsLipid BilayersOligopeptides

Identifiers

PMID39394209
PMCPMC11479646

What Socratic holds

Textmetadata
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 Socratic graph.