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Wnt-11 and Fz7 reduce cell adhesion in convergent extension by sequestration of PAPC and C-cadherin
Wnt-11/planar cell polarity signaling polarizes mesodermal cells undergoing convergent extension during Xenopus laevis gastrulation. These shape changes associated with lateral intercalation behavior require a dynamic modulation of cell adhesion. In this paper, we report that Wnt-11/frizzled-7 (Fz7)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514027/ https://www.ncbi.nlm.nih.gov/pubmed/22908314 http://dx.doi.org/10.1083/jcb.201110076 |
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author | Kraft, Bianca Berger, Corinna D. Wallkamm, Veronika Steinbeisser, Herbert Wedlich, Doris |
author_facet | Kraft, Bianca Berger, Corinna D. Wallkamm, Veronika Steinbeisser, Herbert Wedlich, Doris |
author_sort | Kraft, Bianca |
collection | PubMed |
description | Wnt-11/planar cell polarity signaling polarizes mesodermal cells undergoing convergent extension during Xenopus laevis gastrulation. These shape changes associated with lateral intercalation behavior require a dynamic modulation of cell adhesion. In this paper, we report that Wnt-11/frizzled-7 (Fz7) controls cell adhesion by forming separate adhesion-modulating complexes (AMCs) with the paraxial protocadherin (PAPC; denoted as AMCP) and C-cadherin (denoted as AMCC) via distinct Fz7 interaction domains. When PAPC was part of a Wnt-11–Fz7 complex, its Dynamin1- and clathrin-dependent internalization was blocked. This membrane stabilization of AMCP (Fz7/PAPC) by Wnt-11 prevented C-cadherin clustering, resulting in reduced cell adhesion and modified cell sorting activity. Importantly, Wnt-11 did not influence C-cadherin internalization; instead, it promoted the formation of AMCC (Fz7/Cadherin), which competed with cis-dimerization of C-cadherin. Because PAPC and C-cadherin did not directly interact and did not form a joint complex with Fz7, we suggest that Wnt-11 triggers the formation of two distinct complexes, AMCC and AMCP, that act in parallel to reduce cell adhesion by hampering lateral clustering of C-cadherin. |
format | Online Article Text |
id | pubmed-3514027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35140272013-02-20 Wnt-11 and Fz7 reduce cell adhesion in convergent extension by sequestration of PAPC and C-cadherin Kraft, Bianca Berger, Corinna D. Wallkamm, Veronika Steinbeisser, Herbert Wedlich, Doris J Cell Biol Research Articles Wnt-11/planar cell polarity signaling polarizes mesodermal cells undergoing convergent extension during Xenopus laevis gastrulation. These shape changes associated with lateral intercalation behavior require a dynamic modulation of cell adhesion. In this paper, we report that Wnt-11/frizzled-7 (Fz7) controls cell adhesion by forming separate adhesion-modulating complexes (AMCs) with the paraxial protocadherin (PAPC; denoted as AMCP) and C-cadherin (denoted as AMCC) via distinct Fz7 interaction domains. When PAPC was part of a Wnt-11–Fz7 complex, its Dynamin1- and clathrin-dependent internalization was blocked. This membrane stabilization of AMCP (Fz7/PAPC) by Wnt-11 prevented C-cadherin clustering, resulting in reduced cell adhesion and modified cell sorting activity. Importantly, Wnt-11 did not influence C-cadherin internalization; instead, it promoted the formation of AMCC (Fz7/Cadherin), which competed with cis-dimerization of C-cadherin. Because PAPC and C-cadherin did not directly interact and did not form a joint complex with Fz7, we suggest that Wnt-11 triggers the formation of two distinct complexes, AMCC and AMCP, that act in parallel to reduce cell adhesion by hampering lateral clustering of C-cadherin. The Rockefeller University Press 2012-08-20 /pmc/articles/PMC3514027/ /pubmed/22908314 http://dx.doi.org/10.1083/jcb.201110076 Text en © 2012 Kraft et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Kraft, Bianca Berger, Corinna D. Wallkamm, Veronika Steinbeisser, Herbert Wedlich, Doris Wnt-11 and Fz7 reduce cell adhesion in convergent extension by sequestration of PAPC and C-cadherin |
title | Wnt-11 and Fz7 reduce cell adhesion in convergent extension by
sequestration of PAPC and C-cadherin |
title_full | Wnt-11 and Fz7 reduce cell adhesion in convergent extension by
sequestration of PAPC and C-cadherin |
title_fullStr | Wnt-11 and Fz7 reduce cell adhesion in convergent extension by
sequestration of PAPC and C-cadherin |
title_full_unstemmed | Wnt-11 and Fz7 reduce cell adhesion in convergent extension by
sequestration of PAPC and C-cadherin |
title_short | Wnt-11 and Fz7 reduce cell adhesion in convergent extension by
sequestration of PAPC and C-cadherin |
title_sort | wnt-11 and fz7 reduce cell adhesion in convergent extension by
sequestration of papc and c-cadherin |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514027/ https://www.ncbi.nlm.nih.gov/pubmed/22908314 http://dx.doi.org/10.1083/jcb.201110076 |
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