Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function

Abstract Tight junction complexes are involved in the establishment and maintenance of cell polarity and the regulation of signalling pathways, controlling biological processes such as cell differentiation and cell proliferation. MarvelD3 is a tight junction protein expressed in adult epithelial and...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Charlotte Heymans, Ophélie Delcorte, Catherine Spourquet, Mylah Villacorte-Tabelin, Sébastien Dupasquier, Younes Achouri, Siam Mahibullah, Pascale Lemoine, Maria S. Balda, Karl Matter, Christophe E. Pierreux
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/2f0bd55705b64e16964177485120a440
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:2f0bd55705b64e16964177485120a440
record_format dspace
spelling oai:doaj.org-article:2f0bd55705b64e16964177485120a4402021-12-02T15:33:14ZSpatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function10.1038/s41598-021-93654-22045-2322https://doaj.org/article/2f0bd55705b64e16964177485120a4402021-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-93654-2https://doaj.org/toc/2045-2322Abstract Tight junction complexes are involved in the establishment and maintenance of cell polarity and the regulation of signalling pathways, controlling biological processes such as cell differentiation and cell proliferation. MarvelD3 is a tight junction protein expressed in adult epithelial and endothelial cells. In Xenopus laevis, MarvelD3 morphants present differentiation defects of several ectodermal derivatives. In vitro experiments further revealed that MarvelD3 couples tight junctions to the MEKK1-JNK pathway to regulate cell behaviour and survival. In this work, we found that MarvelD3 is expressed from early developmental stages in the exocrine and endocrine compartments of the pancreas, as well as in endothelial cells of this organ. We thoroughly characterized MarvelD3 expression pattern in developing pancreas and evaluated its function by genetic ablation. Surprisingly, inactivation of MarvelD3 in mice did not alter development and differentiation of the pancreatic tissue. Moreover, tight junction formation and organization, cell polarization, and activity of the JNK-pathway were not impacted by the deletion of MarvelD3.Charlotte HeymansOphélie DelcorteCatherine SpourquetMylah Villacorte-TabelinSébastien DupasquierYounes AchouriSiam MahibullahPascale LemoineMaria S. BaldaKarl MatterChristophe E. PierreuxNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Charlotte Heymans
Ophélie Delcorte
Catherine Spourquet
Mylah Villacorte-Tabelin
Sébastien Dupasquier
Younes Achouri
Siam Mahibullah
Pascale Lemoine
Maria S. Balda
Karl Matter
Christophe E. Pierreux
Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function
description Abstract Tight junction complexes are involved in the establishment and maintenance of cell polarity and the regulation of signalling pathways, controlling biological processes such as cell differentiation and cell proliferation. MarvelD3 is a tight junction protein expressed in adult epithelial and endothelial cells. In Xenopus laevis, MarvelD3 morphants present differentiation defects of several ectodermal derivatives. In vitro experiments further revealed that MarvelD3 couples tight junctions to the MEKK1-JNK pathway to regulate cell behaviour and survival. In this work, we found that MarvelD3 is expressed from early developmental stages in the exocrine and endocrine compartments of the pancreas, as well as in endothelial cells of this organ. We thoroughly characterized MarvelD3 expression pattern in developing pancreas and evaluated its function by genetic ablation. Surprisingly, inactivation of MarvelD3 in mice did not alter development and differentiation of the pancreatic tissue. Moreover, tight junction formation and organization, cell polarization, and activity of the JNK-pathway were not impacted by the deletion of MarvelD3.
format article
author Charlotte Heymans
Ophélie Delcorte
Catherine Spourquet
Mylah Villacorte-Tabelin
Sébastien Dupasquier
Younes Achouri
Siam Mahibullah
Pascale Lemoine
Maria S. Balda
Karl Matter
Christophe E. Pierreux
author_facet Charlotte Heymans
Ophélie Delcorte
Catherine Spourquet
Mylah Villacorte-Tabelin
Sébastien Dupasquier
Younes Achouri
Siam Mahibullah
Pascale Lemoine
Maria S. Balda
Karl Matter
Christophe E. Pierreux
author_sort Charlotte Heymans
title Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function
title_short Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function
title_full Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function
title_fullStr Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function
title_full_unstemmed Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function
title_sort spatio-temporal expression pattern and role of the tight junction protein marveld3 in pancreas development and function
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/2f0bd55705b64e16964177485120a440
work_keys_str_mv AT charlotteheymans spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT opheliedelcorte spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT catherinespourquet spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT mylahvillacortetabelin spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT sebastiendupasquier spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT younesachouri spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT siammahibullah spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT pascalelemoine spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT mariasbalda spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT karlmatter spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
AT christopheepierreux spatiotemporalexpressionpatternandroleofthetightjunctionproteinmarveld3inpancreasdevelopmentandfunction
_version_ 1718387073350631424