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Primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis
The tendon enthesis is a fibrocartilaginous tissue critical for transfer of muscle forces to bone. Enthesis pathologies are common, and surgical repair of tendon to bone is plagued by high failure rates. At the root of these failures is a gap in knowledge of how the tendon enthesis is formed and mai...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608799/ https://www.ncbi.nlm.nih.gov/pubmed/33127677 http://dx.doi.org/10.1126/sciadv.abc1799 |
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author | Fang, Fei Schwartz, Andrea G. Moore, Emily R. Sup, McKenzie E. Thomopoulos, Stavros |
author_facet | Fang, Fei Schwartz, Andrea G. Moore, Emily R. Sup, McKenzie E. Thomopoulos, Stavros |
author_sort | Fang, Fei |
collection | PubMed |
description | The tendon enthesis is a fibrocartilaginous tissue critical for transfer of muscle forces to bone. Enthesis pathologies are common, and surgical repair of tendon to bone is plagued by high failure rates. At the root of these failures is a gap in knowledge of how the tendon enthesis is formed and maintained. We tested the hypothesis that the primary cilium is a hub for transducing biophysical and hedgehog (Hh) signals to regulate tendon enthesis formation and adaptation to loading. Primary cilia were necessary for enthesis development, and cilia assembly was coincident with Hh signaling and enthesis mineralization. Cilia responded inversely to loading; increased loading led to decreased cilia and decreased loading led to increased cilia. Enthesis responses to loading were dependent on Hh signaling through cilia. Results imply a role for tendon enthesis primary cilia as mechanical responders and Hh signal transducers, providing a therapeutic target for tendon enthesis pathologies. |
format | Online Article Text |
id | pubmed-7608799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-76087992020-11-13 Primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis Fang, Fei Schwartz, Andrea G. Moore, Emily R. Sup, McKenzie E. Thomopoulos, Stavros Sci Adv Research Articles The tendon enthesis is a fibrocartilaginous tissue critical for transfer of muscle forces to bone. Enthesis pathologies are common, and surgical repair of tendon to bone is plagued by high failure rates. At the root of these failures is a gap in knowledge of how the tendon enthesis is formed and maintained. We tested the hypothesis that the primary cilium is a hub for transducing biophysical and hedgehog (Hh) signals to regulate tendon enthesis formation and adaptation to loading. Primary cilia were necessary for enthesis development, and cilia assembly was coincident with Hh signaling and enthesis mineralization. Cilia responded inversely to loading; increased loading led to decreased cilia and decreased loading led to increased cilia. Enthesis responses to loading were dependent on Hh signaling through cilia. Results imply a role for tendon enthesis primary cilia as mechanical responders and Hh signal transducers, providing a therapeutic target for tendon enthesis pathologies. American Association for the Advancement of Science 2020-10-30 /pmc/articles/PMC7608799/ /pubmed/33127677 http://dx.doi.org/10.1126/sciadv.abc1799 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Fang, Fei Schwartz, Andrea G. Moore, Emily R. Sup, McKenzie E. Thomopoulos, Stavros Primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis |
title | Primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis |
title_full | Primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis |
title_fullStr | Primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis |
title_full_unstemmed | Primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis |
title_short | Primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis |
title_sort | primary cilia as the nexus of biophysical and hedgehog signaling at the tendon enthesis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608799/ https://www.ncbi.nlm.nih.gov/pubmed/33127677 http://dx.doi.org/10.1126/sciadv.abc1799 |
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