Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/202705
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dc.contributor.authorKechagia, Zanetta-
dc.contributor.authorSáez, Pablo-
dc.contributor.authorGómez González, Manuel-
dc.contributor.authorCanales, Brenda-
dc.contributor.authorViswanadha, Srivatsava-
dc.contributor.authorZamarbide, Martín-
dc.contributor.authorAndreu, Ion-
dc.contributor.authorKoorman, Thijs-
dc.contributor.authorBeedle, Amy E. M.-
dc.contributor.authorElosegui Artola, Alberto-
dc.contributor.authorDerksen, Patrick W. B.-
dc.contributor.authorTrepat Guixer, Xavier-
dc.contributor.authorArroyo, Marino-
dc.contributor.authorRoca-Cusachs Soulere, Pere-
dc.date.accessioned2023-10-09T12:00:08Z-
dc.date.available2023-10-09T12:00:08Z-
dc.date.issued2023-09-14-
dc.identifier.issn1476-4660-
dc.identifier.urihttps://hdl.handle.net/2445/202705-
dc.description.abstractThe mechanical properties of the extracellular matrix dictate tissue behaviour. In epithelial tissues, laminin is a very abundant extracellular matrix component and a key supporting element. Here we show that laminin hinders the mechanoresponses of breast epithelial cells by shielding the nucleus from mechanical deformation. Coating substrates with laminin-111-unlike fibronectin or collagen I-impairs cell response to substrate rigidity and YAP nuclear localization. Blocking the laminin-specific integrin β4 increases nuclear YAP ratios in a rigidity-dependent manner without affecting the cell forces or focal adhesions. By combining mechanical perturbations and mathematical modelling, we show that β4 integrins establish a mechanical linkage between the substrate and keratin cytoskeleton, which stiffens the network and shields the nucleus from actomyosin-mediated mechanical deformation. In turn, this affects the nuclear YAP mechanoresponses, chromatin methylation and cell invasion in three dimensions. Our results demonstrate a mechanism by which tissues can regulate their sensitivity to mechanical signals.© 2023. The Author(s).-
dc.format.extent34 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Nature Limited-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/s41563-023-01657-3-
dc.relation.ispartofNature Materials, 2023, vol. 22, p. 1409–1420-
dc.relation.urihttps://doi.org/10.1038/s41563-023-01657-3-
dc.rightscc by (c) Kechagia, Zanetta et al., 2023-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC))-
dc.subject.classificationCèl·lules epitelials-
dc.subject.classificationGlicoproteïnes-
dc.subject.classificationEpithelial cells-
dc.subject.classificationBiomecànica-
dc.subject.otherGlycoproteins-
dc.subject.otherBiomechanics-
dc.titleThe laminin-keratin link shields the nucleus from mechanical deformation and signalling-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2023-10-09T10:48:37Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.idimarina6602549-
dc.identifier.pmid37709930-
Appears in Collections:Articles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC))

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