Inside-out regulation of E-cadherin conformation and adhesion
- 22 July 2021
- journal article
- research article
- Published by National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 118 (30)
Abstract
Significance: Cadherin cell–cell adhesion proteins play key roles in the formation and maintenance of tissues. Their adhesion is carefully regulated to orchestrate complex movement of cells. While cadherin ectodomains bind in two conformations with different adhesive properties, the mechanisms by which cells regulate the conformation (and consequently adhesion) of individual cadherins are unknown. Here, we demonstrate that the association of intracellular vinculin with the cadherin cytoplasmic region regulates cadherin adhesion by switching ectodomains from a weak binding to the strongly adhesive conformation. In contrast to the prevailing view which suggests that vinculin regulates adhesion solely by remodeling the cytoskeleton, we show that vinculin can directly modulate single cadherin ectodomain conformation and this process is mediated by changes in cytoskeletal tension.Keywords
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Funding Information
- HHS | NIH | National Institute of General Medical Sciences (R01GM121885)
- HHS | NIH | National Institute of General Medical Sciences (R01GM133880)
- National Science Foundation (PHY-1607550)
- HHS | NIH | National Institute of Biomedical Imaging and Bioengineering (R03EB021636)
- National Science Foundation (1562095)
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (016.Vidi.189.166)
This publication has 70 references indexed in Scilit:
- α-Catenin and Vinculin Cooperate to Promote High E-cadherin-based Adhesion StrengthJournal of Biological Chemistry, 2013
- Ideal, catch, and slip bonds in cadherin adhesionProceedings of the National Academy of Sciences, 2012
- E-cadherin is under constitutive actomyosin-generated tension that is increased at cell–cell contacts upon externally applied stretchProceedings of the National Academy of Sciences, 2012
- αE-catenin is an autoinhibited molecule that coactivates vinculinProceedings of the National Academy of Sciences, 2012
- Allosteric Cross Talk between Cadherin Extracellular DomainsBiophysical Journal, 2010
- Two-step adhesive binding by classical cadherinsNature Structural & Molecular Biology, 2010
- Loss of α-Catenin Decreases the Strength of Single E-cadherin Bonds between Human Cancer CellsJournal of Biological Chemistry, 2009
- Resolving cadherin interactions and binding cooperativity at the single-molecule levelProceedings of the National Academy of Sciences, 2009
- α-Catenin mediates initial E-cadherin-dependent cell–cell recognition and subsequent bond strengtheningProceedings of the National Academy of Sciences, 2008
- The Crystal Structure of Human E-cadherin Domains 1 and 2, and Comparison with other Cadherins in the Context of Adhesion MechanismJournal of Molecular Biology, 2007