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Mesenchymal stem cells for cartilage regeneration in dogs

Articular cartilage damage and osteoarthritis (OA) are common orthopedic diseases in both humans and dogs. Once damaged, the articular cartilage seldom undergoes spontaneous repair because of its avascular, aneural, and alymphatic state, and the damage progresses to a chronic and painful situation....

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Autores principales: Sasaki, Akari, Mizuno, Mitsuru, Mochizuki, Manabu, Sekiya, Ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545524/
https://www.ncbi.nlm.nih.gov/pubmed/31171954
http://dx.doi.org/10.4252/wjsc.v11.i5.254
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author Sasaki, Akari
Mizuno, Mitsuru
Mochizuki, Manabu
Sekiya, Ichiro
author_facet Sasaki, Akari
Mizuno, Mitsuru
Mochizuki, Manabu
Sekiya, Ichiro
author_sort Sasaki, Akari
collection PubMed
description Articular cartilage damage and osteoarthritis (OA) are common orthopedic diseases in both humans and dogs. Once damaged, the articular cartilage seldom undergoes spontaneous repair because of its avascular, aneural, and alymphatic state, and the damage progresses to a chronic and painful situation. Dogs have distinctive characteristics compared to other laboratory animal species in that they share an OA pathology with humans. Dogs can also require treatment for naturally developed OA; therefore, effective treatment methods for OA are desired in veterinary medicine as well as in human medicine. Recently, interest has grown in regenerative medicine that includes the use of mesenchymal stem cells (MSCs). In cartilage repair, MSCs are a promising therapeutic tool due to their self-renewal capacity, ability to differentiate into cartilage, potential for trophic factor production, and capacity for immunomodulation. The MSCs from dogs (canine MSCs; cMSCs) share various characteristics with MSCs from other animal species, but they show some deviations, particularly in their differentiation ability and surface epitope expression. In vivo studies of cMSCs have demonstrated that intraarticular cMSC injection into cartilage lesions results in excellent hyaline cartilage regeneration. In clinical situations, cMSCs have shown great therapeutic effects, including amelioration of pain and lameness in dogs suffering from OA. However, some issues remain, such as a lack of regulations or guidelines and a need for unified methods for the use of cMSCs. This review summarizes what is known about cMSCs, including their in vitro characteristics, their therapeutic effects in cartilage lesion treatment in preclinical in vivo studies, their clinical efficacy for treatment of naturally developed OA in dogs, and the current limitations of cMSC studies.
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spelling pubmed-65455242019-06-06 Mesenchymal stem cells for cartilage regeneration in dogs Sasaki, Akari Mizuno, Mitsuru Mochizuki, Manabu Sekiya, Ichiro World J Stem Cells Review Articular cartilage damage and osteoarthritis (OA) are common orthopedic diseases in both humans and dogs. Once damaged, the articular cartilage seldom undergoes spontaneous repair because of its avascular, aneural, and alymphatic state, and the damage progresses to a chronic and painful situation. Dogs have distinctive characteristics compared to other laboratory animal species in that they share an OA pathology with humans. Dogs can also require treatment for naturally developed OA; therefore, effective treatment methods for OA are desired in veterinary medicine as well as in human medicine. Recently, interest has grown in regenerative medicine that includes the use of mesenchymal stem cells (MSCs). In cartilage repair, MSCs are a promising therapeutic tool due to their self-renewal capacity, ability to differentiate into cartilage, potential for trophic factor production, and capacity for immunomodulation. The MSCs from dogs (canine MSCs; cMSCs) share various characteristics with MSCs from other animal species, but they show some deviations, particularly in their differentiation ability and surface epitope expression. In vivo studies of cMSCs have demonstrated that intraarticular cMSC injection into cartilage lesions results in excellent hyaline cartilage regeneration. In clinical situations, cMSCs have shown great therapeutic effects, including amelioration of pain and lameness in dogs suffering from OA. However, some issues remain, such as a lack of regulations or guidelines and a need for unified methods for the use of cMSCs. This review summarizes what is known about cMSCs, including their in vitro characteristics, their therapeutic effects in cartilage lesion treatment in preclinical in vivo studies, their clinical efficacy for treatment of naturally developed OA in dogs, and the current limitations of cMSC studies. Baishideng Publishing Group Inc 2019-05-26 2019-05-26 /pmc/articles/PMC6545524/ /pubmed/31171954 http://dx.doi.org/10.4252/wjsc.v11.i5.254 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Review
Sasaki, Akari
Mizuno, Mitsuru
Mochizuki, Manabu
Sekiya, Ichiro
Mesenchymal stem cells for cartilage regeneration in dogs
title Mesenchymal stem cells for cartilage regeneration in dogs
title_full Mesenchymal stem cells for cartilage regeneration in dogs
title_fullStr Mesenchymal stem cells for cartilage regeneration in dogs
title_full_unstemmed Mesenchymal stem cells for cartilage regeneration in dogs
title_short Mesenchymal stem cells for cartilage regeneration in dogs
title_sort mesenchymal stem cells for cartilage regeneration in dogs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545524/
https://www.ncbi.nlm.nih.gov/pubmed/31171954
http://dx.doi.org/10.4252/wjsc.v11.i5.254
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