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Regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model

Although rotator cuff disease is a common cause of shoulder pain, there is still no treatment method that could halt or reveres its development and progression. The purpose of this study was to investigate the efficacy of umbilical cord-derived mesenchymal stem cells (UC MSCs) on the regeneration of...

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Autores principales: Yea, Ji-Hye, Kim, InJa, Sym, Gayoung, Park, Jin-Kyung, Lee, Ah-Young, Cho, Byeong Chan, Bae, Tae Soo, Kim, Byoung Jae, Jo, Chris Hyunchul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652329/
https://www.ncbi.nlm.nih.gov/pubmed/33166292
http://dx.doi.org/10.1371/journal.pone.0235239
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author Yea, Ji-Hye
Kim, InJa
Sym, Gayoung
Park, Jin-Kyung
Lee, Ah-Young
Cho, Byeong Chan
Bae, Tae Soo
Kim, Byoung Jae
Jo, Chris Hyunchul
author_facet Yea, Ji-Hye
Kim, InJa
Sym, Gayoung
Park, Jin-Kyung
Lee, Ah-Young
Cho, Byeong Chan
Bae, Tae Soo
Kim, Byoung Jae
Jo, Chris Hyunchul
author_sort Yea, Ji-Hye
collection PubMed
description Although rotator cuff disease is a common cause of shoulder pain, there is still no treatment method that could halt or reveres its development and progression. The purpose of this study was to investigate the efficacy of umbilical cord-derived mesenchymal stem cells (UC MSCs) on the regeneration of a full-thickness rotator cuff defect (FTD) in a rat model. We injected either UC MSCs or saline to the FTD and investigated macroscopic, histological and biomechanical results and cell trafficking. Treatment with UC MSCs improved macroscopic appearance in terms of tendon thickness at two weeks, and inflammation, defect size, swelling/redness and connection surrounding tissue and slidability at four weeks compared to the saline group. Histologically, UC MSCs induced the tendon matrix formation recovering collagen organization, nuclear aspect ratio and orientation angle of fibroblast as well as suppressing cartilage-related glycosaminoglycan compared to saline group at four weeks. The UC MSCs group also improved ultimate failure load by 25.0% and 19.0% and ultimate stress by 27.3% and 26.8% at two and four weeks compared to saline group. UC MSCs labeled with PKH26 exhibited 5.3% survival at four weeks compared to three hours after injection. This study demonstrated that UC MSCs regenerated the FTD with tendon tissue similar properties to the normal tendon in terms of macroscopic, histological and biomechanical characteristics in a rat model.
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spelling pubmed-76523292020-11-18 Regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model Yea, Ji-Hye Kim, InJa Sym, Gayoung Park, Jin-Kyung Lee, Ah-Young Cho, Byeong Chan Bae, Tae Soo Kim, Byoung Jae Jo, Chris Hyunchul PLoS One Research Article Although rotator cuff disease is a common cause of shoulder pain, there is still no treatment method that could halt or reveres its development and progression. The purpose of this study was to investigate the efficacy of umbilical cord-derived mesenchymal stem cells (UC MSCs) on the regeneration of a full-thickness rotator cuff defect (FTD) in a rat model. We injected either UC MSCs or saline to the FTD and investigated macroscopic, histological and biomechanical results and cell trafficking. Treatment with UC MSCs improved macroscopic appearance in terms of tendon thickness at two weeks, and inflammation, defect size, swelling/redness and connection surrounding tissue and slidability at four weeks compared to the saline group. Histologically, UC MSCs induced the tendon matrix formation recovering collagen organization, nuclear aspect ratio and orientation angle of fibroblast as well as suppressing cartilage-related glycosaminoglycan compared to saline group at four weeks. The UC MSCs group also improved ultimate failure load by 25.0% and 19.0% and ultimate stress by 27.3% and 26.8% at two and four weeks compared to saline group. UC MSCs labeled with PKH26 exhibited 5.3% survival at four weeks compared to three hours after injection. This study demonstrated that UC MSCs regenerated the FTD with tendon tissue similar properties to the normal tendon in terms of macroscopic, histological and biomechanical characteristics in a rat model. Public Library of Science 2020-11-09 /pmc/articles/PMC7652329/ /pubmed/33166292 http://dx.doi.org/10.1371/journal.pone.0235239 Text en © 2020 Yea et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yea, Ji-Hye
Kim, InJa
Sym, Gayoung
Park, Jin-Kyung
Lee, Ah-Young
Cho, Byeong Chan
Bae, Tae Soo
Kim, Byoung Jae
Jo, Chris Hyunchul
Regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model
title Regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model
title_full Regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model
title_fullStr Regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model
title_full_unstemmed Regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model
title_short Regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model
title_sort regeneration of a full-thickness defect in rotator cuff tendon with umbilical cord-derived mesenchymal stem cells in a rat model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652329/
https://www.ncbi.nlm.nih.gov/pubmed/33166292
http://dx.doi.org/10.1371/journal.pone.0235239
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