The laminin-keratin link shields the nucleus from mechanical deformation and signalling

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.date.updated2023-10-09T10:48:37Z
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.identifier.idimarina6602549
dc.identifier.issn1476-4660
dc.identifier.pmid37709930
dc.identifier.urihttps://hdl.handle.net/2445/202705
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.accessRightsinfo:eu-repo/semantics/openAccess
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

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