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Inducible progenitor-derived Wingless regulates adult midgut regeneration in Drosophila

The ability to regenerate following stress is a hallmark of self-renewing tissues. However, little is known about how regeneration differs from homeostatic tissue maintenance. Here, we study the role and regulation of Wingless (Wg)/Wnt signalling during intestinal regeneration using the Drosophila a...

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Autores principales: Cordero, Julia B, Stefanatos, Rhoda K, Scopelliti, Alessandro, Vidal, Marcos, Sansom, Owen J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463851/
https://www.ncbi.nlm.nih.gov/pubmed/22948071
http://dx.doi.org/10.1038/emboj.2012.248
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author Cordero, Julia B
Stefanatos, Rhoda K
Scopelliti, Alessandro
Vidal, Marcos
Sansom, Owen J
author_facet Cordero, Julia B
Stefanatos, Rhoda K
Scopelliti, Alessandro
Vidal, Marcos
Sansom, Owen J
author_sort Cordero, Julia B
collection PubMed
description The ability to regenerate following stress is a hallmark of self-renewing tissues. However, little is known about how regeneration differs from homeostatic tissue maintenance. Here, we study the role and regulation of Wingless (Wg)/Wnt signalling during intestinal regeneration using the Drosophila adult midgut. We show that Wg is produced by the intestinal epithelial compartment upon damage or stress and it is exclusively required for intestinal stem cell (ISC) proliferation during tissue regeneration. Reducing Wg or downstream signalling components from the intestinal epithelium blocked tissue regeneration. Importantly, we demonstrate that Wg from the undifferentiated progenitor cell, the enteroblast, is required for Myc-dependent ISC proliferation during regeneration. Similar to young regenerating tissues, ageing intestines required Wg and Myc for ISC hyperproliferation. Unexpectedly, our results demonstrate that epithelial but not mesenchymal Wg is essential for ISC proliferation in response to damage, while neither source of the ligand is solely responsible for ISC maintenance and tissue self-renewal in unchallenged tissues. Therefore, fine-tuning Wnt results in optimal balance between the ability to respond to stress without negatively affecting organismal viability.
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spelling pubmed-34638512012-10-04 Inducible progenitor-derived Wingless regulates adult midgut regeneration in Drosophila Cordero, Julia B Stefanatos, Rhoda K Scopelliti, Alessandro Vidal, Marcos Sansom, Owen J EMBO J Article The ability to regenerate following stress is a hallmark of self-renewing tissues. However, little is known about how regeneration differs from homeostatic tissue maintenance. Here, we study the role and regulation of Wingless (Wg)/Wnt signalling during intestinal regeneration using the Drosophila adult midgut. We show that Wg is produced by the intestinal epithelial compartment upon damage or stress and it is exclusively required for intestinal stem cell (ISC) proliferation during tissue regeneration. Reducing Wg or downstream signalling components from the intestinal epithelium blocked tissue regeneration. Importantly, we demonstrate that Wg from the undifferentiated progenitor cell, the enteroblast, is required for Myc-dependent ISC proliferation during regeneration. Similar to young regenerating tissues, ageing intestines required Wg and Myc for ISC hyperproliferation. Unexpectedly, our results demonstrate that epithelial but not mesenchymal Wg is essential for ISC proliferation in response to damage, while neither source of the ligand is solely responsible for ISC maintenance and tissue self-renewal in unchallenged tissues. Therefore, fine-tuning Wnt results in optimal balance between the ability to respond to stress without negatively affecting organismal viability. European Molecular Biology Organization 2012-10-03 2012-09-04 /pmc/articles/PMC3463851/ /pubmed/22948071 http://dx.doi.org/10.1038/emboj.2012.248 Text en Copyright © 2012, European Molecular Biology Organization https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial Share Alike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Article
Cordero, Julia B
Stefanatos, Rhoda K
Scopelliti, Alessandro
Vidal, Marcos
Sansom, Owen J
Inducible progenitor-derived Wingless regulates adult midgut regeneration in Drosophila
title Inducible progenitor-derived Wingless regulates adult midgut regeneration in Drosophila
title_full Inducible progenitor-derived Wingless regulates adult midgut regeneration in Drosophila
title_fullStr Inducible progenitor-derived Wingless regulates adult midgut regeneration in Drosophila
title_full_unstemmed Inducible progenitor-derived Wingless regulates adult midgut regeneration in Drosophila
title_short Inducible progenitor-derived Wingless regulates adult midgut regeneration in Drosophila
title_sort inducible progenitor-derived wingless regulates adult midgut regeneration in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463851/
https://www.ncbi.nlm.nih.gov/pubmed/22948071
http://dx.doi.org/10.1038/emboj.2012.248
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