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

The 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 fr...

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Detalhes bibliográficos
Autores: Kechagia, Zanetta, Sáez, Pablo, Gómez González, Manuel, Canales, Brenda, Viswanadha, Srivatsava, Zamarbide, Martín, Andreu, Ion, Koorman, Thijs, Beedle, Amy E. M., Elosegui Artola, Alberto, Derksen, Patrick W. B., Trepat Guixer, Xavier, Arroyo, Marino, Roca-Cusachs Soulere, Pere
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/202705
Acesso em linha:https://hdl.handle.net/2445/202705
Access Level:acceso abierto
Palavra-chave:Cèl·lules epitelials
Glicoproteïnes
Biomecànica
Epithelial cells
Glycoproteins
Biomechanics
Descrição
Resumo:The 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).