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PAPC mediates self/non–self-distinction during Snail1-dependent tissue separation

Cleft-like boundaries represent a type of cell sorting boundary characterized by the presence of a physical gap between tissues. We studied the cleft-like ectoderm–mesoderm boundary in Xenopus laevis and zebrafish gastrulae. We identified the transcription factor Snail1 as being essential for tissue...

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Autores principales: Luu, Olivia, Damm, Erich W., Parent, Serge E., Barua, Debanjan, Smith, Tamara H.L., Wen, Jason W.H., Lepage, Stephanie E., Nagel, Martina, Ibrahim-Gawel, Hady, Huang, Yunyun, Bruce, Ashley E.E., Winklbauer, Rudolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362454/
https://www.ncbi.nlm.nih.gov/pubmed/25778923
http://dx.doi.org/10.1083/jcb.201409026
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author Luu, Olivia
Damm, Erich W.
Parent, Serge E.
Barua, Debanjan
Smith, Tamara H.L.
Wen, Jason W.H.
Lepage, Stephanie E.
Nagel, Martina
Ibrahim-Gawel, Hady
Huang, Yunyun
Bruce, Ashley E.E.
Winklbauer, Rudolf
author_facet Luu, Olivia
Damm, Erich W.
Parent, Serge E.
Barua, Debanjan
Smith, Tamara H.L.
Wen, Jason W.H.
Lepage, Stephanie E.
Nagel, Martina
Ibrahim-Gawel, Hady
Huang, Yunyun
Bruce, Ashley E.E.
Winklbauer, Rudolf
author_sort Luu, Olivia
collection PubMed
description Cleft-like boundaries represent a type of cell sorting boundary characterized by the presence of a physical gap between tissues. We studied the cleft-like ectoderm–mesoderm boundary in Xenopus laevis and zebrafish gastrulae. We identified the transcription factor Snail1 as being essential for tissue separation, showed that its expression in the mesoderm depends on noncanonical Wnt signaling, and demonstrated that it enables paraxial protocadherin (PAPC) to promote tissue separation through two novel functions. First, PAPC attenuates planar cell polarity signaling at the ectoderm–mesoderm boundary to lower cell adhesion and facilitate cleft formation. Second, PAPC controls formation of a distinct type of adhesive contact between mesoderm and ectoderm cells that shows properties of a cleft-like boundary at the single-cell level. It consists of short stretches of adherens junction–like contacts inserted between intermediate-sized contacts and large intercellular gaps. These roles of PAPC constitute a self/non–self-recognition mechanism that determines the site of boundary formation at the interface between PAPC-expressing and -nonexpressing cells.
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spelling pubmed-43624542015-09-16 PAPC mediates self/non–self-distinction during Snail1-dependent tissue separation Luu, Olivia Damm, Erich W. Parent, Serge E. Barua, Debanjan Smith, Tamara H.L. Wen, Jason W.H. Lepage, Stephanie E. Nagel, Martina Ibrahim-Gawel, Hady Huang, Yunyun Bruce, Ashley E.E. Winklbauer, Rudolf J Cell Biol Research Articles Cleft-like boundaries represent a type of cell sorting boundary characterized by the presence of a physical gap between tissues. We studied the cleft-like ectoderm–mesoderm boundary in Xenopus laevis and zebrafish gastrulae. We identified the transcription factor Snail1 as being essential for tissue separation, showed that its expression in the mesoderm depends on noncanonical Wnt signaling, and demonstrated that it enables paraxial protocadherin (PAPC) to promote tissue separation through two novel functions. First, PAPC attenuates planar cell polarity signaling at the ectoderm–mesoderm boundary to lower cell adhesion and facilitate cleft formation. Second, PAPC controls formation of a distinct type of adhesive contact between mesoderm and ectoderm cells that shows properties of a cleft-like boundary at the single-cell level. It consists of short stretches of adherens junction–like contacts inserted between intermediate-sized contacts and large intercellular gaps. These roles of PAPC constitute a self/non–self-recognition mechanism that determines the site of boundary formation at the interface between PAPC-expressing and -nonexpressing cells. The Rockefeller University Press 2015-03-16 /pmc/articles/PMC4362454/ /pubmed/25778923 http://dx.doi.org/10.1083/jcb.201409026 Text en © 2015 Luu 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
Luu, Olivia
Damm, Erich W.
Parent, Serge E.
Barua, Debanjan
Smith, Tamara H.L.
Wen, Jason W.H.
Lepage, Stephanie E.
Nagel, Martina
Ibrahim-Gawel, Hady
Huang, Yunyun
Bruce, Ashley E.E.
Winklbauer, Rudolf
PAPC mediates self/non–self-distinction during Snail1-dependent tissue separation
title PAPC mediates self/non–self-distinction during Snail1-dependent tissue separation
title_full PAPC mediates self/non–self-distinction during Snail1-dependent tissue separation
title_fullStr PAPC mediates self/non–self-distinction during Snail1-dependent tissue separation
title_full_unstemmed PAPC mediates self/non–self-distinction during Snail1-dependent tissue separation
title_short PAPC mediates self/non–self-distinction during Snail1-dependent tissue separation
title_sort papc mediates self/non–self-distinction during snail1-dependent tissue separation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362454/
https://www.ncbi.nlm.nih.gov/pubmed/25778923
http://dx.doi.org/10.1083/jcb.201409026
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