Author
Listed:
- Rahul P. Langhe
(Zoological Institute, Cell and Developmental Biology, Karlsruhe Institute of Technology (KIT)
Present address: Institute of Neuroscience Paris-Saclay, UMR CNRS 9197, Université Paris-Sud, Orsay, France)
- Tetyana Gudzenko
(Center for Functional Nanostructures, Karlsruhe Institute of Technology (KIT))
- Michael Bachmann
(Zoological Institute, Cell and Neurobiology Biology, Karlsruhe Institute of Technology (KIT))
- Sarah F. Becker
(Zoological Institute, Cell and Developmental Biology, Karlsruhe Institute of Technology (KIT)
Present address: Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), CNRS UMR7104, INSERM U964, Université de Strasbourg, 1 rue Laurent Fries, 67404 Illkirch Cu Strasbourg, France)
- Carina Gonnermann
(Center for Functional Nanostructures, Karlsruhe Institute of Technology (KIT))
- Claudia Winter
(Zoological Institute, Cell and Developmental Biology, Karlsruhe Institute of Technology (KIT))
- Genevieve Abbruzzese
(University of Massachusetts)
- Dominique Alfandari
(University of Massachusetts)
- Marie-Claire Kratzer
(Zoological Institute, Cell and Developmental Biology, Karlsruhe Institute of Technology (KIT)
Laboratory for Applications of Synchrotron Radiation, Karlsruhe Institute of Technology (KIT))
- Clemens M. Franz
(Center for Functional Nanostructures, Karlsruhe Institute of Technology (KIT))
- Jubin Kashef
(Zoological Institute, Cell and Developmental Biology, Karlsruhe Institute of Technology (KIT)
Institute for Photon Science and Synchrotron Radiation, Karlsruhe Institute of Technology (KIT))
Abstract
Cadherin receptors have a well-established role in cell–cell adhesion, cell polarization and differentiation. However, some cadherins also promote cell and tissue movement during embryonic development and tumour progression. In particular, cadherin-11 is upregulated during tumour and inflammatory cell invasion, but the mechanisms underlying cadherin-11 stimulated cell migration are still incompletely understood. Here, we show that cadherin-11 localizes to focal adhesions and promotes adhesion to fibronectin in Xenopus neural crest, a highly migratory embryonic cell population. Transfected cadherin-11 also localizes to focal adhesions in different mammalian cell lines, while endogenous cadherin-11 shows focal adhesion localization in primary human fibroblasts. In focal adhesions, cadherin-11 co-localizes with β1-integrin and paxillin and physically interacts with the fibronectin-binding proteoglycan syndecan-4. Adhesion to fibronectin mediated by cadherin-11/syndecan-4 complexes requires both the extracellular domain of syndecan-4, and the transmembrane and cytoplasmic domains of cadherin-11. These results reveal an unexpected role of a classical cadherin in cell–matrix adhesion during cell migration.
Suggested Citation
Rahul P. Langhe & Tetyana Gudzenko & Michael Bachmann & Sarah F. Becker & Carina Gonnermann & Claudia Winter & Genevieve Abbruzzese & Dominique Alfandari & Marie-Claire Kratzer & Clemens M. Franz & Ju, 2016.
"Cadherin-11 localizes to focal adhesions and promotes cell–substrate adhesion,"
Nature Communications, Nature, vol. 7(1), pages 1-10, April.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10909
DOI: 10.1038/ncomms10909
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10909. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.