Cargando…

VASP, zyxin and TES are tension-dependent members of Focal Adherens Junctions independent of the α-catenin-vinculin module

Mechanical forces are integrated at cadherin-based adhesion complexes to regulate morphology and strength of cell-cell junctions and organization of associated F-actin. A central mechanosensor at the cadherin complex is α-catenin, whose stretching recruits vinculin to regulate adhesion strength. The...

Descripción completa

Detalles Bibliográficos
Autores principales: Oldenburg, Joppe, van der Krogt, Gerard, Twiss, Floor, Bongaarts, Annika, Habani, Yasmin, Slotman, Johan A., Houtsmuller, Adriaan, Huveneers, Stephan, de Rooij, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661603/
https://www.ncbi.nlm.nih.gov/pubmed/26611125
http://dx.doi.org/10.1038/srep17225
_version_ 1782403007270354944
author Oldenburg, Joppe
van der Krogt, Gerard
Twiss, Floor
Bongaarts, Annika
Habani, Yasmin
Slotman, Johan A.
Houtsmuller, Adriaan
Huveneers, Stephan
de Rooij, Johan
author_facet Oldenburg, Joppe
van der Krogt, Gerard
Twiss, Floor
Bongaarts, Annika
Habani, Yasmin
Slotman, Johan A.
Houtsmuller, Adriaan
Huveneers, Stephan
de Rooij, Johan
author_sort Oldenburg, Joppe
collection PubMed
description Mechanical forces are integrated at cadherin-based adhesion complexes to regulate morphology and strength of cell-cell junctions and organization of associated F-actin. A central mechanosensor at the cadherin complex is α-catenin, whose stretching recruits vinculin to regulate adhesion strength. The identity of the F-actin regulating signals that are also activated by mechanical forces at cadherin-based junctions has remained elusive. Here we identify the actin-regulators VASP, zyxin and TES as members of punctate, tensile cadherin-based junctions called Focal Adherens Junctions (FAJ) and show that they display mechanosensitive recruitment similar to that of vinculin. However, this recruitment is not altered by destroying or over-activating the α-catenin/vinculin module. Structured Illumination Microscopy (SIM) indicates that these tension sensitive proteins concentrate at locations within FAJs that are distinct from the core cadherin complex proteins. Furthermore, localization studies using mutated versions of VASP and zyxin indicate that these two proteins require binding to each other in order to localize to the FAJs. We conclude that there are multiple force sensitive modules present at the FAJ that are activated at distinct locations along the cadherin-F-actin axis and regulate specific aspects of junction dynamics.
format Online
Article
Text
id pubmed-4661603
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-46616032015-12-01 VASP, zyxin and TES are tension-dependent members of Focal Adherens Junctions independent of the α-catenin-vinculin module Oldenburg, Joppe van der Krogt, Gerard Twiss, Floor Bongaarts, Annika Habani, Yasmin Slotman, Johan A. Houtsmuller, Adriaan Huveneers, Stephan de Rooij, Johan Sci Rep Article Mechanical forces are integrated at cadherin-based adhesion complexes to regulate morphology and strength of cell-cell junctions and organization of associated F-actin. A central mechanosensor at the cadherin complex is α-catenin, whose stretching recruits vinculin to regulate adhesion strength. The identity of the F-actin regulating signals that are also activated by mechanical forces at cadherin-based junctions has remained elusive. Here we identify the actin-regulators VASP, zyxin and TES as members of punctate, tensile cadherin-based junctions called Focal Adherens Junctions (FAJ) and show that they display mechanosensitive recruitment similar to that of vinculin. However, this recruitment is not altered by destroying or over-activating the α-catenin/vinculin module. Structured Illumination Microscopy (SIM) indicates that these tension sensitive proteins concentrate at locations within FAJs that are distinct from the core cadherin complex proteins. Furthermore, localization studies using mutated versions of VASP and zyxin indicate that these two proteins require binding to each other in order to localize to the FAJs. We conclude that there are multiple force sensitive modules present at the FAJ that are activated at distinct locations along the cadherin-F-actin axis and regulate specific aspects of junction dynamics. Nature Publishing Group 2015-11-27 /pmc/articles/PMC4661603/ /pubmed/26611125 http://dx.doi.org/10.1038/srep17225 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Oldenburg, Joppe
van der Krogt, Gerard
Twiss, Floor
Bongaarts, Annika
Habani, Yasmin
Slotman, Johan A.
Houtsmuller, Adriaan
Huveneers, Stephan
de Rooij, Johan
VASP, zyxin and TES are tension-dependent members of Focal Adherens Junctions independent of the α-catenin-vinculin module
title VASP, zyxin and TES are tension-dependent members of Focal Adherens Junctions independent of the α-catenin-vinculin module
title_full VASP, zyxin and TES are tension-dependent members of Focal Adherens Junctions independent of the α-catenin-vinculin module
title_fullStr VASP, zyxin and TES are tension-dependent members of Focal Adherens Junctions independent of the α-catenin-vinculin module
title_full_unstemmed VASP, zyxin and TES are tension-dependent members of Focal Adherens Junctions independent of the α-catenin-vinculin module
title_short VASP, zyxin and TES are tension-dependent members of Focal Adherens Junctions independent of the α-catenin-vinculin module
title_sort vasp, zyxin and tes are tension-dependent members of focal adherens junctions independent of the α-catenin-vinculin module
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661603/
https://www.ncbi.nlm.nih.gov/pubmed/26611125
http://dx.doi.org/10.1038/srep17225
work_keys_str_mv AT oldenburgjoppe vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule
AT vanderkrogtgerard vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule
AT twissfloor vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule
AT bongaartsannika vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule
AT habaniyasmin vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule
AT slotmanjohana vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule
AT houtsmulleradriaan vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule
AT huveneersstephan vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule
AT derooijjohan vaspzyxinandtesaretensiondependentmembersoffocaladherensjunctionsindependentoftheacateninvinculinmodule