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Efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen I scaffold

OBJECTIVES: Our main objective was to biologically improve rotator cuff healing in an elderly rat model using mesenchymal stem cells (MSCs) in combination with a collagen membrane and compared against other current techniques. METHODS: A chronic rotator cuff tear injury model was developed by unilat...

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Autores principales: Tornero-Esteban, Pilar, Hoyas, José Antonio, Villafuertes, Esther, Rodríguez-Bobada, Cruz, López-Gordillo, Yamila, Rojo, Francisco J., Guinea, Gustavo V., Paleczny, Anna, Lópiz-Morales, Yaiza, Rodriguez-Rodriguez, Luis, Marco, Fernando, Fernández-Gutiérrez, Benjamín
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535284/
https://www.ncbi.nlm.nih.gov/pubmed/26268217
http://dx.doi.org/10.1186/s13018-015-0269-6
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author Tornero-Esteban, Pilar
Hoyas, José Antonio
Villafuertes, Esther
Rodríguez-Bobada, Cruz
López-Gordillo, Yamila
Rojo, Francisco J.
Guinea, Gustavo V.
Paleczny, Anna
Lópiz-Morales, Yaiza
Rodriguez-Rodriguez, Luis
Marco, Fernando
Fernández-Gutiérrez, Benjamín
author_facet Tornero-Esteban, Pilar
Hoyas, José Antonio
Villafuertes, Esther
Rodríguez-Bobada, Cruz
López-Gordillo, Yamila
Rojo, Francisco J.
Guinea, Gustavo V.
Paleczny, Anna
Lópiz-Morales, Yaiza
Rodriguez-Rodriguez, Luis
Marco, Fernando
Fernández-Gutiérrez, Benjamín
author_sort Tornero-Esteban, Pilar
collection PubMed
description OBJECTIVES: Our main objective was to biologically improve rotator cuff healing in an elderly rat model using mesenchymal stem cells (MSCs) in combination with a collagen membrane and compared against other current techniques. METHODS: A chronic rotator cuff tear injury model was developed by unilaterally detaching the supraspinatus (SP) tendons of Sprague-Dawley rats. At 1 month postinjury, the tears were repaired using one of the following techniques: (a) classical surgery using sutures (n = 12), (b) type I collagen membranes (n = 15), and (c) type I collagen membranes + 1 × 106 allogeneic MSCs (n = 14). Lesion restoration was evaluated at 1, 2, and 3 months postinjury based on biomechanical criteria. Continuous variables were described using mean and standard deviation (SD). To analyse the effect of the different surgical treatments in the repaired tendons’ biomechanical capabilities (maximum load, stiffness, and deformity), a two-way ANOVA model was used, introducing an interaction between such factor and time (1, 2, and 3 months postinjury). RESULTS: With regard to maximum load, we observed an almost significant interaction between treatment and time (F = 2.62, df = 4, p = 0.053). When we analysed how this biomechanical capability changed with time for each treatment, we observed that repair with OrthADAPT and MSCs was associated with a significant increase in maximum load (p = 0.04) between months 1 and 3. On the other hand, when we compared the different treatments among themselves at different time points, we observed that the repair with OrthADAPT and MSCs has associated with a significant higher maximum load, when compared with the use of suture, but only at 3 months (p = 0.014). With regard to stiffness and deformity, no significant interaction was observed (F = 1.68, df = 4, p = 0.18; F = 0.40, df = 4, p = 0.81; respectively). CONCLUSIONS: The implantation of MSCs along with a collagen I scaffold into surgically created tendon defects is safe and effective. MSCs improved the tendon’s maximum load over time, indicating that MSCs could help facilitate the dynamic process of tendon repair.
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spelling pubmed-45352842015-08-14 Efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen I scaffold Tornero-Esteban, Pilar Hoyas, José Antonio Villafuertes, Esther Rodríguez-Bobada, Cruz López-Gordillo, Yamila Rojo, Francisco J. Guinea, Gustavo V. Paleczny, Anna Lópiz-Morales, Yaiza Rodriguez-Rodriguez, Luis Marco, Fernando Fernández-Gutiérrez, Benjamín J Orthop Surg Res Research Article OBJECTIVES: Our main objective was to biologically improve rotator cuff healing in an elderly rat model using mesenchymal stem cells (MSCs) in combination with a collagen membrane and compared against other current techniques. METHODS: A chronic rotator cuff tear injury model was developed by unilaterally detaching the supraspinatus (SP) tendons of Sprague-Dawley rats. At 1 month postinjury, the tears were repaired using one of the following techniques: (a) classical surgery using sutures (n = 12), (b) type I collagen membranes (n = 15), and (c) type I collagen membranes + 1 × 106 allogeneic MSCs (n = 14). Lesion restoration was evaluated at 1, 2, and 3 months postinjury based on biomechanical criteria. Continuous variables were described using mean and standard deviation (SD). To analyse the effect of the different surgical treatments in the repaired tendons’ biomechanical capabilities (maximum load, stiffness, and deformity), a two-way ANOVA model was used, introducing an interaction between such factor and time (1, 2, and 3 months postinjury). RESULTS: With regard to maximum load, we observed an almost significant interaction between treatment and time (F = 2.62, df = 4, p = 0.053). When we analysed how this biomechanical capability changed with time for each treatment, we observed that repair with OrthADAPT and MSCs was associated with a significant increase in maximum load (p = 0.04) between months 1 and 3. On the other hand, when we compared the different treatments among themselves at different time points, we observed that the repair with OrthADAPT and MSCs has associated with a significant higher maximum load, when compared with the use of suture, but only at 3 months (p = 0.014). With regard to stiffness and deformity, no significant interaction was observed (F = 1.68, df = 4, p = 0.18; F = 0.40, df = 4, p = 0.81; respectively). CONCLUSIONS: The implantation of MSCs along with a collagen I scaffold into surgically created tendon defects is safe and effective. MSCs improved the tendon’s maximum load over time, indicating that MSCs could help facilitate the dynamic process of tendon repair. BioMed Central 2015-08-14 /pmc/articles/PMC4535284/ /pubmed/26268217 http://dx.doi.org/10.1186/s13018-015-0269-6 Text en © Tornero-Esteban et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Tornero-Esteban, Pilar
Hoyas, José Antonio
Villafuertes, Esther
Rodríguez-Bobada, Cruz
López-Gordillo, Yamila
Rojo, Francisco J.
Guinea, Gustavo V.
Paleczny, Anna
Lópiz-Morales, Yaiza
Rodriguez-Rodriguez, Luis
Marco, Fernando
Fernández-Gutiérrez, Benjamín
Efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen I scaffold
title Efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen I scaffold
title_full Efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen I scaffold
title_fullStr Efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen I scaffold
title_full_unstemmed Efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen I scaffold
title_short Efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen I scaffold
title_sort efficacy of supraspinatus tendon repair using mesenchymal stem cells along with a collagen i scaffold
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535284/
https://www.ncbi.nlm.nih.gov/pubmed/26268217
http://dx.doi.org/10.1186/s13018-015-0269-6
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