Cargando…

Immunomodulation of Pluripotent Stem Cell-Derived Mesenchymal Stem Cells in Rotator Cuff Tears Model

Background: Rotator cuff tears (RCTs) induce chronic muscle weakness and shoulder pain. Treatment of RCT using surgery or drugs causes lipid infiltration and fibrosis, which hampers tissue regeneration and complete recovery. The pluripotent stem cell-derived multipotent mesenchymal stem cells (M-MSC...

Descripción completa

Detalles Bibliográficos
Autores principales: Baek, Jieun, Ryu, Bokyeong, Kim, Jin, Lee, Seul-Gi, Oh, Min-Seok, Hong, Ki-Sung, Kim, Eun-Young, Kim, C-Yoon, Chung, Hyung-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312476/
https://www.ncbi.nlm.nih.gov/pubmed/35884853
http://dx.doi.org/10.3390/biomedicines10071549
_version_ 1784753849898106880
author Baek, Jieun
Ryu, Bokyeong
Kim, Jin
Lee, Seul-Gi
Oh, Min-Seok
Hong, Ki-Sung
Kim, Eun-Young
Kim, C-Yoon
Chung, Hyung-Min
author_facet Baek, Jieun
Ryu, Bokyeong
Kim, Jin
Lee, Seul-Gi
Oh, Min-Seok
Hong, Ki-Sung
Kim, Eun-Young
Kim, C-Yoon
Chung, Hyung-Min
author_sort Baek, Jieun
collection PubMed
description Background: Rotator cuff tears (RCTs) induce chronic muscle weakness and shoulder pain. Treatment of RCT using surgery or drugs causes lipid infiltration and fibrosis, which hampers tissue regeneration and complete recovery. The pluripotent stem cell-derived multipotent mesenchymal stem cells (M-MSCs) represent potential candidate next-generation therapies for RCT. Methods: The difference between M-MSCs and adult-MSCs was compared and analyzed using next-generation sequencing (NGS). In addition, using a rat model of RCT, the muscle recovery ability of M-MSCs and adult-MSCs was evaluated by conducting a histological analysis and monitoring the cytokine expression level. Results: Using NGS, it was confirmed that M-MSC was suitable for transplantation because of its excellent ability to regulate inflammation that promotes tissue repair and reduced apoptosis and rejection during transplantation. In addition, while M-MSCs persisted for up to 8 weeks in vivo, they significantly reduced inflammation and adipogenesis-related cytokine levels in rat muscle. Significant differences were also confirmed in histopathological remission. Conclusions: M-MSCs remain in the body longer to modulate immune responses in RCTs and have a greater potential to improve muscle recovery by alleviating acute inflammatory responses. This indicates that M-MSCs could be used in potential next-generation RCT therapies.
format Online
Article
Text
id pubmed-9312476
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93124762022-07-26 Immunomodulation of Pluripotent Stem Cell-Derived Mesenchymal Stem Cells in Rotator Cuff Tears Model Baek, Jieun Ryu, Bokyeong Kim, Jin Lee, Seul-Gi Oh, Min-Seok Hong, Ki-Sung Kim, Eun-Young Kim, C-Yoon Chung, Hyung-Min Biomedicines Article Background: Rotator cuff tears (RCTs) induce chronic muscle weakness and shoulder pain. Treatment of RCT using surgery or drugs causes lipid infiltration and fibrosis, which hampers tissue regeneration and complete recovery. The pluripotent stem cell-derived multipotent mesenchymal stem cells (M-MSCs) represent potential candidate next-generation therapies for RCT. Methods: The difference between M-MSCs and adult-MSCs was compared and analyzed using next-generation sequencing (NGS). In addition, using a rat model of RCT, the muscle recovery ability of M-MSCs and adult-MSCs was evaluated by conducting a histological analysis and monitoring the cytokine expression level. Results: Using NGS, it was confirmed that M-MSC was suitable for transplantation because of its excellent ability to regulate inflammation that promotes tissue repair and reduced apoptosis and rejection during transplantation. In addition, while M-MSCs persisted for up to 8 weeks in vivo, they significantly reduced inflammation and adipogenesis-related cytokine levels in rat muscle. Significant differences were also confirmed in histopathological remission. Conclusions: M-MSCs remain in the body longer to modulate immune responses in RCTs and have a greater potential to improve muscle recovery by alleviating acute inflammatory responses. This indicates that M-MSCs could be used in potential next-generation RCT therapies. MDPI 2022-06-29 /pmc/articles/PMC9312476/ /pubmed/35884853 http://dx.doi.org/10.3390/biomedicines10071549 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Baek, Jieun
Ryu, Bokyeong
Kim, Jin
Lee, Seul-Gi
Oh, Min-Seok
Hong, Ki-Sung
Kim, Eun-Young
Kim, C-Yoon
Chung, Hyung-Min
Immunomodulation of Pluripotent Stem Cell-Derived Mesenchymal Stem Cells in Rotator Cuff Tears Model
title Immunomodulation of Pluripotent Stem Cell-Derived Mesenchymal Stem Cells in Rotator Cuff Tears Model
title_full Immunomodulation of Pluripotent Stem Cell-Derived Mesenchymal Stem Cells in Rotator Cuff Tears Model
title_fullStr Immunomodulation of Pluripotent Stem Cell-Derived Mesenchymal Stem Cells in Rotator Cuff Tears Model
title_full_unstemmed Immunomodulation of Pluripotent Stem Cell-Derived Mesenchymal Stem Cells in Rotator Cuff Tears Model
title_short Immunomodulation of Pluripotent Stem Cell-Derived Mesenchymal Stem Cells in Rotator Cuff Tears Model
title_sort immunomodulation of pluripotent stem cell-derived mesenchymal stem cells in rotator cuff tears model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312476/
https://www.ncbi.nlm.nih.gov/pubmed/35884853
http://dx.doi.org/10.3390/biomedicines10071549
work_keys_str_mv AT baekjieun immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel
AT ryubokyeong immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel
AT kimjin immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel
AT leeseulgi immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel
AT ohminseok immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel
AT hongkisung immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel
AT kimeunyoung immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel
AT kimcyoon immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel
AT chunghyungmin immunomodulationofpluripotentstemcellderivedmesenchymalstemcellsinrotatorcufftearsmodel