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An E-cadherin-actin clutch translates the mechanical force of cortical flow for cell-cell contact to inhibit epithelial cell locomotion.
Noordstra, Ivar; Hermoso, Mario Díez; Schimmel, Lilian; Bonfim-Melo, Alexis; Currin-Ross, Denni; Duong, Cao Nguyen; Kalappurakkal, Joseph Mathew; Morris, Richard G; Vestweber, Dietmar; Mayor, Satyajit; Gordon, Emma; Roca-Cusachs, Pere; Yap, Alpha S.
Afiliação
  • Noordstra I; Centre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia.
  • Hermoso MD; Institute for Bioengineering of Catalonia (IBEC), the Barcelona Institute of Technology (BIST), 08028 Barcelona, Spain.
  • Schimmel L; Centre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia.
  • Bonfim-Melo A; Centre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia.
  • Currin-Ross D; Centre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia; School of Physics & EMBL Australia Node in Single Molecule Science, School of Biomedical Sciences, University of New South Wales, Sydney, NSW 20
  • Duong CN; Department of Vascular Biology, Max Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.
  • Kalappurakkal JM; National Centre for Biological Science, Tata Institute for Fundamental Research, Bangalore 560065, India.
  • Morris RG; School of Physics & EMBL Australia Node in Single Molecule Science, School of Biomedical Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
  • Vestweber D; Department of Vascular Biology, Max Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.
  • Mayor S; National Centre for Biological Science, Tata Institute for Fundamental Research, Bangalore 560065, India.
  • Gordon E; Centre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia.
  • Roca-Cusachs P; Institute for Bioengineering of Catalonia (IBEC), the Barcelona Institute of Technology (BIST), 08028 Barcelona, Spain; Universitat de Barcelona, 08036 Barcelona, Spain. Electronic address: proca@ibecbarcelona.eu.
  • Yap AS; Centre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia. Electronic address: a.yap@uq.edu.au.
Dev Cell ; 58(18): 1748-1763.e6, 2023 09 25.
Article em En | MEDLINE | ID: mdl-37480844
ABSTRACT
Adherens junctions (AJs) allow cell contact to inhibit epithelial migration yet also permit epithelia to move as coherent sheets. How, then, do cells identify which contacts will inhibit locomotion? Here, we show that in human epithelial cells this arises from the orientation of cortical flows at AJs. When the leader cells from different migrating sheets make head-on contact with one another, they assemble AJs that couple together oppositely directed cortical flows. This applies a tensile signal to the actin-binding domain (ABD) of α-catenin, which provides a clutch to promote lateral adhesion growth and inhibit the lamellipodial activity necessary for migration. In contrast, AJs found between leader cells in the same migrating sheet have cortical flows aligned in the same direction, and no such mechanical inhibition takes place. Therefore, α-catenin mechanosensitivity in the clutch between E-cadherin and cortical F-actin allows cells to interpret the direction of motion via cortical flows and signal for contact to inhibit locomotion.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article