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Ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis

Restoring the native structure of the tendon enthesis, where collagen fibers of the midsubstance are integrated within a fibrocartilaginous structure, is problematic following injury. As current surgical methods fail to restore this region adequately, engineers, biologists, and clinicians are workin...

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Autores principales: Breidenbach, Andrew P., Aschbacher‐Smith, Lindsey, Lu, Yinhui, Dyment, Nathaniel A., Liu, Chia‐Feng, Liu, Han, Wylie, Chris, Rao, Marepalli, Shearn, Jason T., Rowe, David W., Kadler, Karl E., Jiang, Rulang, Butler, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706742/
https://www.ncbi.nlm.nih.gov/pubmed/25807894
http://dx.doi.org/10.1002/jor.22899
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author Breidenbach, Andrew P.
Aschbacher‐Smith, Lindsey
Lu, Yinhui
Dyment, Nathaniel A.
Liu, Chia‐Feng
Liu, Han
Wylie, Chris
Rao, Marepalli
Shearn, Jason T.
Rowe, David W.
Kadler, Karl E.
Jiang, Rulang
Butler, David L.
author_facet Breidenbach, Andrew P.
Aschbacher‐Smith, Lindsey
Lu, Yinhui
Dyment, Nathaniel A.
Liu, Chia‐Feng
Liu, Han
Wylie, Chris
Rao, Marepalli
Shearn, Jason T.
Rowe, David W.
Kadler, Karl E.
Jiang, Rulang
Butler, David L.
author_sort Breidenbach, Andrew P.
collection PubMed
description Restoring the native structure of the tendon enthesis, where collagen fibers of the midsubstance are integrated within a fibrocartilaginous structure, is problematic following injury. As current surgical methods fail to restore this region adequately, engineers, biologists, and clinicians are working to understand how this structure forms as a prerequisite to improving repair outcomes. We recently reported on the role of Indian hedgehog (Ihh), a novel enthesis marker, in regulating early postnatal enthesis formation. Here, we investigate how inactivating the Hh pathway in tendon cells affects adult (12‐week) murine patellar tendon (PT) enthesis mechanics, fibrocartilage morphology, and collagen fiber organization. We show that ablating Hh signaling resulted in greater than 100% increased failure insertion strain (0.10 v. 0.05 mm/mm, p<0.01) as well as sub‐failure biomechanical deficiencies. Although collagen fiber orientation appears overtly normal in the midsubstance, ablating Hh signaling reduces mineralized fibrocartilage by 32%, leading to less collagen embedded within mineralized tissue. Ablating Hh signaling also caused collagen fibers to coalesce at the insertion, which may explain in part the increased strains. These results indicate that Ihh signaling plays a critical role in the mineralization process of fibrocartilaginous entheses and may be a novel therapeutic to promote tendon‐to‐bone healing. © 2015 The Authors. Journal of Orthopaedic Research published by Wiley Periodicals, Inc. on behalf of the Orthopaedic Research Society. J Orthop Res 33:1142–1151, 2015.
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spelling pubmed-47067422016-08-01 Ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis Breidenbach, Andrew P. Aschbacher‐Smith, Lindsey Lu, Yinhui Dyment, Nathaniel A. Liu, Chia‐Feng Liu, Han Wylie, Chris Rao, Marepalli Shearn, Jason T. Rowe, David W. Kadler, Karl E. Jiang, Rulang Butler, David L. J Orthop Res Research Articles Restoring the native structure of the tendon enthesis, where collagen fibers of the midsubstance are integrated within a fibrocartilaginous structure, is problematic following injury. As current surgical methods fail to restore this region adequately, engineers, biologists, and clinicians are working to understand how this structure forms as a prerequisite to improving repair outcomes. We recently reported on the role of Indian hedgehog (Ihh), a novel enthesis marker, in regulating early postnatal enthesis formation. Here, we investigate how inactivating the Hh pathway in tendon cells affects adult (12‐week) murine patellar tendon (PT) enthesis mechanics, fibrocartilage morphology, and collagen fiber organization. We show that ablating Hh signaling resulted in greater than 100% increased failure insertion strain (0.10 v. 0.05 mm/mm, p<0.01) as well as sub‐failure biomechanical deficiencies. Although collagen fiber orientation appears overtly normal in the midsubstance, ablating Hh signaling reduces mineralized fibrocartilage by 32%, leading to less collagen embedded within mineralized tissue. Ablating Hh signaling also caused collagen fibers to coalesce at the insertion, which may explain in part the increased strains. These results indicate that Ihh signaling plays a critical role in the mineralization process of fibrocartilaginous entheses and may be a novel therapeutic to promote tendon‐to‐bone healing. © 2015 The Authors. Journal of Orthopaedic Research published by Wiley Periodicals, Inc. on behalf of the Orthopaedic Research Society. J Orthop Res 33:1142–1151, 2015. John Wiley and Sons Inc. 2015-04-14 2015-08 /pmc/articles/PMC4706742/ /pubmed/25807894 http://dx.doi.org/10.1002/jor.22899 Text en © 2015 The Authors. Journal of Orthopaedic Research published by Wiley Periodicals, Inc. on behalf of the Orthopaedic Research Society. This is an open access article under the terms of the Creative Commons Attribution (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 Research Articles
Breidenbach, Andrew P.
Aschbacher‐Smith, Lindsey
Lu, Yinhui
Dyment, Nathaniel A.
Liu, Chia‐Feng
Liu, Han
Wylie, Chris
Rao, Marepalli
Shearn, Jason T.
Rowe, David W.
Kadler, Karl E.
Jiang, Rulang
Butler, David L.
Ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis
title Ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis
title_full Ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis
title_fullStr Ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis
title_full_unstemmed Ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis
title_short Ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis
title_sort ablating hedgehog signaling in tenocytes during development impairs biomechanics and matrix organization of the adult murine patellar tendon enthesis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706742/
https://www.ncbi.nlm.nih.gov/pubmed/25807894
http://dx.doi.org/10.1002/jor.22899
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