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Tissue-Engineered Tendon for Enthesis Regeneration in a Rat Rotator Cuff Model

Healing of rotator cuff (RC) injuries with current suture or augmented scaffold techniques fails to regenerate the enthesis and instead forms a weaker fibrovascular scar that is prone to subsequent failure. Regeneration of the enthesis is the key to improving clinical outcomes for RC injuries. We hy...

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Autores principales: Smietana, Michael J., Moncada-Larrotiz, Pablo, Arruda, Ellen M., Bedi, Asheesh, Larkin, Lisa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515124/
https://www.ncbi.nlm.nih.gov/pubmed/28736687
http://dx.doi.org/10.1089/biores.2016.0042
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author Smietana, Michael J.
Moncada-Larrotiz, Pablo
Arruda, Ellen M.
Bedi, Asheesh
Larkin, Lisa M.
author_facet Smietana, Michael J.
Moncada-Larrotiz, Pablo
Arruda, Ellen M.
Bedi, Asheesh
Larkin, Lisa M.
author_sort Smietana, Michael J.
collection PubMed
description Healing of rotator cuff (RC) injuries with current suture or augmented scaffold techniques fails to regenerate the enthesis and instead forms a weaker fibrovascular scar that is prone to subsequent failure. Regeneration of the enthesis is the key to improving clinical outcomes for RC injuries. We hypothesized that the utilization of our tissue-engineered tendon to repair either an acute or a chronic full-thickness supraspinatus tear would regenerate a functional enthesis and return the biomechanics of the tendon back to that found in native tissue. Engineered tendons were fabricated from bone marrow-derived mesenchymal stem cells utilizing our well-described fabrication technology. Forty-three rats underwent unilateral detachment of the supraspinatus tendon followed by acute (immediate) or chronic (4 weeks retracted) repair by using either our engineered tendon or a trans-osseous suture technique. Animals were sacrificed at 8 weeks. Biomechanical and histological analyses of the regenerated enthesis and tendon were performed. Statistical analysis was performed by using a one-way analysis of variance with significance set at p < 0.05. Acute repairs using engineered tendon had improved enthesis structure and lower biomechanical failures compared with suture repairs. Chronic repairs with engineered tendon had a more native-like enthesis with increased fibrocartilage formation, reduced scar formation, and lower biomechanical failure compared with suture repair. Thus, the utilization of our tissue-engineered tendon showed improve enthesis regeneration and improved function in chronic RC repairs compared with suture repair. Clinical Significance: Our engineered tendon construct shows promise as a clinically relevant method for repair of RC injuries.
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spelling pubmed-55151242017-07-21 Tissue-Engineered Tendon for Enthesis Regeneration in a Rat Rotator Cuff Model Smietana, Michael J. Moncada-Larrotiz, Pablo Arruda, Ellen M. Bedi, Asheesh Larkin, Lisa M. Biores Open Access Original Research Article Healing of rotator cuff (RC) injuries with current suture or augmented scaffold techniques fails to regenerate the enthesis and instead forms a weaker fibrovascular scar that is prone to subsequent failure. Regeneration of the enthesis is the key to improving clinical outcomes for RC injuries. We hypothesized that the utilization of our tissue-engineered tendon to repair either an acute or a chronic full-thickness supraspinatus tear would regenerate a functional enthesis and return the biomechanics of the tendon back to that found in native tissue. Engineered tendons were fabricated from bone marrow-derived mesenchymal stem cells utilizing our well-described fabrication technology. Forty-three rats underwent unilateral detachment of the supraspinatus tendon followed by acute (immediate) or chronic (4 weeks retracted) repair by using either our engineered tendon or a trans-osseous suture technique. Animals were sacrificed at 8 weeks. Biomechanical and histological analyses of the regenerated enthesis and tendon were performed. Statistical analysis was performed by using a one-way analysis of variance with significance set at p < 0.05. Acute repairs using engineered tendon had improved enthesis structure and lower biomechanical failures compared with suture repairs. Chronic repairs with engineered tendon had a more native-like enthesis with increased fibrocartilage formation, reduced scar formation, and lower biomechanical failure compared with suture repair. Thus, the utilization of our tissue-engineered tendon showed improve enthesis regeneration and improved function in chronic RC repairs compared with suture repair. Clinical Significance: Our engineered tendon construct shows promise as a clinically relevant method for repair of RC injuries. Mary Ann Liebert, Inc. 2017-06-01 /pmc/articles/PMC5515124/ /pubmed/28736687 http://dx.doi.org/10.1089/biores.2016.0042 Text en © Michael J. Smietana et al. 2017; Published by Mary Ann Liebert, Inc. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Smietana, Michael J.
Moncada-Larrotiz, Pablo
Arruda, Ellen M.
Bedi, Asheesh
Larkin, Lisa M.
Tissue-Engineered Tendon for Enthesis Regeneration in a Rat Rotator Cuff Model
title Tissue-Engineered Tendon for Enthesis Regeneration in a Rat Rotator Cuff Model
title_full Tissue-Engineered Tendon for Enthesis Regeneration in a Rat Rotator Cuff Model
title_fullStr Tissue-Engineered Tendon for Enthesis Regeneration in a Rat Rotator Cuff Model
title_full_unstemmed Tissue-Engineered Tendon for Enthesis Regeneration in a Rat Rotator Cuff Model
title_short Tissue-Engineered Tendon for Enthesis Regeneration in a Rat Rotator Cuff Model
title_sort tissue-engineered tendon for enthesis regeneration in a rat rotator cuff model
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515124/
https://www.ncbi.nlm.nih.gov/pubmed/28736687
http://dx.doi.org/10.1089/biores.2016.0042
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