Myosin VI and vinculin cooperate during the morphogenesis of cadherin cell–cell contacts in mammalian epithelial cells
Open Access
- 30 July 2007
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 178 (3), 529-540
- https://doi.org/10.1083/jcb.200612042
Abstract
Cooperation between cadherins and the actin cytoskeleton controls many aspects of epithelial biogenesis. We report here that myosin VI critically regulates the morphogenesis of epithelial cell–cell contacts. As epithelial monolayers mature in culture, discontinuous cell–cell contacts are initially replaced by continuous (cohesive) contacts. Myosin VI is recruited to cell contacts as they become linear and cohesive, where it forms a biochemical complex with epithelial cadherin (E-cadherin). Myosin VI is necessary for strong cadherin adhesion, for cells to form cohesive linear contacts, and for the integrity of the apical junctional complex. We find that vinculin mediates this effect of myosin VI. Myosin VI is necessary for vinculin and E-cadherin to interact. A combination of gain and loss of function approaches identifies vinculin as a downstream effector of myosin VI that is necessary for the integrity of intercellular contacts. We propose that myosin VI and vinculin form a molecular apparatus that generates cohesive cell–cell contacts in cultured mammalian epithelia.Keywords
This publication has 42 references indexed in Scilit:
- Myosin VI is required for sorting of AP-1B–dependent cargo to the basolateral domain in polarized MDCK cellsThe Journal of cell biology, 2007
- Myosin VI Stabilizes an Actin Network duringDrosophilaSpermatid IndividualizationMolecular Biology of the Cell, 2006
- Ena/VASP Proteins Can Regulate Distinct Modes of Actin Organization at Cadherin-adhesive ContactsMolecular Biology of the Cell, 2006
- Three-Dimensional Structure of Vinculin Bound to Actin FilamentsMolecular Cell, 2006
- The ins and outs of E-cadherin traffickingTrends in Cell Biology, 2004
- Minimal Mutation of the Cytoplasmic Tail Inhibits the Ability of E-cadherin to Activate Rac but Not Phosphatidylinositol 3-Kinase: DIRECT EVIDENCE OF A ROLE FOR CADHERIN-ACTIVATED Rac SIGNALING IN ADHESION AND CONTACT FORMATIONPublished by Elsevier ,2003
- Cadherin-Directed Actin AssemblyCurrent Biology, 2002
- Characterization of Two F‐Actin‐Binding and Oligornerization Sites in the Cell‐Contact Protein VinculinEuropean Journal of Biochemistry, 1997
- F-actin binding site masked by the intramolecular association of vinculin head and tail domainsNature, 1995
- Characterization of an F-actin-binding domain in the cytoskeletal protein vinculin.The Journal of cell biology, 1994