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Ciliary Hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation
How tubular organs elongate is poorly understood. We found that attenuated ciliary Hedgehog signaling in the gut wall impaired patterning of the circumferential smooth muscle and inhibited proliferation and elongation of developing intestine and esophagus. Similarly, ablation of gut-wall smooth musc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664829/ https://www.ncbi.nlm.nih.gov/pubmed/34893605 http://dx.doi.org/10.1038/s41467-021-27319-z |
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author | Yang, Ying Paivinen, Pekka Xie, Chang Krup, Alexis Leigh Makela, Tomi P. Mostov, Keith E. Reiter, Jeremy F. |
author_facet | Yang, Ying Paivinen, Pekka Xie, Chang Krup, Alexis Leigh Makela, Tomi P. Mostov, Keith E. Reiter, Jeremy F. |
author_sort | Yang, Ying |
collection | PubMed |
description | How tubular organs elongate is poorly understood. We found that attenuated ciliary Hedgehog signaling in the gut wall impaired patterning of the circumferential smooth muscle and inhibited proliferation and elongation of developing intestine and esophagus. Similarly, ablation of gut-wall smooth muscle cells reduced lengthening. Disruption of ciliary Hedgehog signaling or removal of smooth muscle reduced residual stress within the gut wall and decreased activity of the mechanotransductive effector YAP. Removing YAP in the mesenchyme also reduced proliferation and elongation, but without affecting smooth muscle formation, suggesting that YAP interprets the smooth muscle-generated force to promote longitudinal growth. Additionally, we developed an intestinal culture system that recapitulates the requirements for cilia and mechanical forces in elongation. Pharmacologically activating YAP in this system restored elongation of cilia-deficient intestines. Thus, our results reveal that ciliary Hedgehog signaling patterns the circumferential smooth muscle to generate radial mechanical forces that activate YAP and elongate the gut. |
format | Online Article Text |
id | pubmed-8664829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86648292021-12-27 Ciliary Hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation Yang, Ying Paivinen, Pekka Xie, Chang Krup, Alexis Leigh Makela, Tomi P. Mostov, Keith E. Reiter, Jeremy F. Nat Commun Article How tubular organs elongate is poorly understood. We found that attenuated ciliary Hedgehog signaling in the gut wall impaired patterning of the circumferential smooth muscle and inhibited proliferation and elongation of developing intestine and esophagus. Similarly, ablation of gut-wall smooth muscle cells reduced lengthening. Disruption of ciliary Hedgehog signaling or removal of smooth muscle reduced residual stress within the gut wall and decreased activity of the mechanotransductive effector YAP. Removing YAP in the mesenchyme also reduced proliferation and elongation, but without affecting smooth muscle formation, suggesting that YAP interprets the smooth muscle-generated force to promote longitudinal growth. Additionally, we developed an intestinal culture system that recapitulates the requirements for cilia and mechanical forces in elongation. Pharmacologically activating YAP in this system restored elongation of cilia-deficient intestines. Thus, our results reveal that ciliary Hedgehog signaling patterns the circumferential smooth muscle to generate radial mechanical forces that activate YAP and elongate the gut. Nature Publishing Group UK 2021-12-10 /pmc/articles/PMC8664829/ /pubmed/34893605 http://dx.doi.org/10.1038/s41467-021-27319-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yang, Ying Paivinen, Pekka Xie, Chang Krup, Alexis Leigh Makela, Tomi P. Mostov, Keith E. Reiter, Jeremy F. Ciliary Hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation |
title | Ciliary Hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation |
title_full | Ciliary Hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation |
title_fullStr | Ciliary Hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation |
title_full_unstemmed | Ciliary Hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation |
title_short | Ciliary Hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation |
title_sort | ciliary hedgehog signaling patterns the digestive system to generate mechanical forces driving elongation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664829/ https://www.ncbi.nlm.nih.gov/pubmed/34893605 http://dx.doi.org/10.1038/s41467-021-27319-z |
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