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Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis

BACKGROUND: Mesenchymal stem cells (MSCs) have a therapeutic potential for the treatment of osteoarthritic (OA) joint pathology and pain. The aims of this study were to determine the influence of a passage number on the effects of MSCs on pain behaviour and cartilage and bone features in a rodent mo...

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Autores principales: Chapman, Victoria, Markides, Hareklea, Sagar, Devi Rani, Xu, Luting, Burston, James J., Mapp, Paul, Kay, Alasdair, Morris, Robert H., Kehoe, Oksana, El Haj, Alicia J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757143/
https://www.ncbi.nlm.nih.gov/pubmed/29434641
http://dx.doi.org/10.1155/2017/2905104
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author Chapman, Victoria
Markides, Hareklea
Sagar, Devi Rani
Xu, Luting
Burston, James J.
Mapp, Paul
Kay, Alasdair
Morris, Robert H.
Kehoe, Oksana
El Haj, Alicia J.
author_facet Chapman, Victoria
Markides, Hareklea
Sagar, Devi Rani
Xu, Luting
Burston, James J.
Mapp, Paul
Kay, Alasdair
Morris, Robert H.
Kehoe, Oksana
El Haj, Alicia J.
author_sort Chapman, Victoria
collection PubMed
description BACKGROUND: Mesenchymal stem cells (MSCs) have a therapeutic potential for the treatment of osteoarthritic (OA) joint pathology and pain. The aims of this study were to determine the influence of a passage number on the effects of MSCs on pain behaviour and cartilage and bone features in a rodent model of OA. METHODS: Rats underwent either medial meniscal transection (MNX) or sham surgery under anaesthesia. Rats received intra-articular injection of either 1.5 × 10(6) late passage MSCs labelled with 10 μg/ml SiMAG, 1.5 × 10(6) late passage mesenchymal stem cells, the steroid Kenalog (200 μg/20 μL), 1.5 × 10(6) early passage MSCs, or serum-free media (SFM). Sham-operated rats received intra-articular injection of SFM. Pain behaviour was quantified until day 42 postmodel induction. Magnetic resonance imaging (MRI) was used to localise the labelled cells within the knee joint. RESULTS: Late passage MSCs and Kenalog attenuated established pain behaviour in MNX rats, but did not alter MNX-induced joint pathology at the end of the study period. Early passage MSCs exacerbated MNX-induced pain behaviour for up to one week postinjection and did not alter joint pathology. CONCLUSION: Our data demonstrate for the first time the role of a passage number in influencing the therapeutic effects of MSCs in a model of OA pain.
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spelling pubmed-57571432018-02-12 Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis Chapman, Victoria Markides, Hareklea Sagar, Devi Rani Xu, Luting Burston, James J. Mapp, Paul Kay, Alasdair Morris, Robert H. Kehoe, Oksana El Haj, Alicia J. Stem Cells Int Research Article BACKGROUND: Mesenchymal stem cells (MSCs) have a therapeutic potential for the treatment of osteoarthritic (OA) joint pathology and pain. The aims of this study were to determine the influence of a passage number on the effects of MSCs on pain behaviour and cartilage and bone features in a rodent model of OA. METHODS: Rats underwent either medial meniscal transection (MNX) or sham surgery under anaesthesia. Rats received intra-articular injection of either 1.5 × 10(6) late passage MSCs labelled with 10 μg/ml SiMAG, 1.5 × 10(6) late passage mesenchymal stem cells, the steroid Kenalog (200 μg/20 μL), 1.5 × 10(6) early passage MSCs, or serum-free media (SFM). Sham-operated rats received intra-articular injection of SFM. Pain behaviour was quantified until day 42 postmodel induction. Magnetic resonance imaging (MRI) was used to localise the labelled cells within the knee joint. RESULTS: Late passage MSCs and Kenalog attenuated established pain behaviour in MNX rats, but did not alter MNX-induced joint pathology at the end of the study period. Early passage MSCs exacerbated MNX-induced pain behaviour for up to one week postinjection and did not alter joint pathology. CONCLUSION: Our data demonstrate for the first time the role of a passage number in influencing the therapeutic effects of MSCs in a model of OA pain. Hindawi 2017 2017-12-24 /pmc/articles/PMC5757143/ /pubmed/29434641 http://dx.doi.org/10.1155/2017/2905104 Text en Copyright © 2017 Victoria Chapman et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chapman, Victoria
Markides, Hareklea
Sagar, Devi Rani
Xu, Luting
Burston, James J.
Mapp, Paul
Kay, Alasdair
Morris, Robert H.
Kehoe, Oksana
El Haj, Alicia J.
Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis
title Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis
title_full Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis
title_fullStr Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis
title_full_unstemmed Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis
title_short Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis
title_sort therapeutic benefit for late, but not early, passage mesenchymal stem cells on pain behaviour in an animal model of osteoarthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757143/
https://www.ncbi.nlm.nih.gov/pubmed/29434641
http://dx.doi.org/10.1155/2017/2905104
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