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Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia
Expression of the Ret receptor tyrosine kinase is a defining feature of enteric neurons. Its importance is underscored by the effects of its mutation in Hirschsprung disease, leading to absence of gut innervation and severe gastrointestinal symptoms. We report a new and physiologically significant s...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641678/ https://www.ncbi.nlm.nih.gov/pubmed/28899900 http://dx.doi.org/10.15252/embj.201696247 |
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author | Perea, Daniel Guiu, Jordi Hudry, Bruno Konstantinidou, Chrysoula Milona, Alexandra Hadjieconomou, Dafni Carroll, Thomas Hoyer, Nina Natarajan, Dipa Kallijärvi, Jukka Walker, James A Soba, Peter Thapar, Nikhil Burns, Alan J Jensen, Kim B Miguel‐Aliaga, Irene |
author_facet | Perea, Daniel Guiu, Jordi Hudry, Bruno Konstantinidou, Chrysoula Milona, Alexandra Hadjieconomou, Dafni Carroll, Thomas Hoyer, Nina Natarajan, Dipa Kallijärvi, Jukka Walker, James A Soba, Peter Thapar, Nikhil Burns, Alan J Jensen, Kim B Miguel‐Aliaga, Irene |
author_sort | Perea, Daniel |
collection | PubMed |
description | Expression of the Ret receptor tyrosine kinase is a defining feature of enteric neurons. Its importance is underscored by the effects of its mutation in Hirschsprung disease, leading to absence of gut innervation and severe gastrointestinal symptoms. We report a new and physiologically significant site of Ret expression in the intestine: the intestinal epithelium. Experiments in Drosophila indicate that Ret is expressed both by enteric neurons and adult intestinal epithelial progenitors, which require Ret to sustain their proliferation. Mechanistically, Ret is engaged in a positive feedback loop with Wnt/Wingless signalling, modulated by Src and Fak kinases. We find that Ret is also expressed by the developing intestinal epithelium of mice, where its expression is maintained into the adult stage in a subset of enteroendocrine/enterochromaffin cells. Mouse organoid experiments point to an intrinsic role for Ret in promoting epithelial maturation and regulating Wnt signalling. Our findings reveal evolutionary conservation of the positive Ret/Wnt signalling feedback in both developmental and homeostatic contexts. They also suggest an epithelial contribution to Ret loss‐of‐function disorders such as Hirschsprung disease. |
format | Online Article Text |
id | pubmed-5641678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56416782017-10-18 Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia Perea, Daniel Guiu, Jordi Hudry, Bruno Konstantinidou, Chrysoula Milona, Alexandra Hadjieconomou, Dafni Carroll, Thomas Hoyer, Nina Natarajan, Dipa Kallijärvi, Jukka Walker, James A Soba, Peter Thapar, Nikhil Burns, Alan J Jensen, Kim B Miguel‐Aliaga, Irene EMBO J Articles Expression of the Ret receptor tyrosine kinase is a defining feature of enteric neurons. Its importance is underscored by the effects of its mutation in Hirschsprung disease, leading to absence of gut innervation and severe gastrointestinal symptoms. We report a new and physiologically significant site of Ret expression in the intestine: the intestinal epithelium. Experiments in Drosophila indicate that Ret is expressed both by enteric neurons and adult intestinal epithelial progenitors, which require Ret to sustain their proliferation. Mechanistically, Ret is engaged in a positive feedback loop with Wnt/Wingless signalling, modulated by Src and Fak kinases. We find that Ret is also expressed by the developing intestinal epithelium of mice, where its expression is maintained into the adult stage in a subset of enteroendocrine/enterochromaffin cells. Mouse organoid experiments point to an intrinsic role for Ret in promoting epithelial maturation and regulating Wnt signalling. Our findings reveal evolutionary conservation of the positive Ret/Wnt signalling feedback in both developmental and homeostatic contexts. They also suggest an epithelial contribution to Ret loss‐of‐function disorders such as Hirschsprung disease. John Wiley and Sons Inc. 2017-09-12 2017-10-16 /pmc/articles/PMC5641678/ /pubmed/28899900 http://dx.doi.org/10.15252/embj.201696247 Text en © 2017 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Perea, Daniel Guiu, Jordi Hudry, Bruno Konstantinidou, Chrysoula Milona, Alexandra Hadjieconomou, Dafni Carroll, Thomas Hoyer, Nina Natarajan, Dipa Kallijärvi, Jukka Walker, James A Soba, Peter Thapar, Nikhil Burns, Alan J Jensen, Kim B Miguel‐Aliaga, Irene Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia |
title | Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia |
title_full | Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia |
title_fullStr | Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia |
title_full_unstemmed | Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia |
title_short | Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia |
title_sort | ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641678/ https://www.ncbi.nlm.nih.gov/pubmed/28899900 http://dx.doi.org/10.15252/embj.201696247 |
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