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Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair
Frontiers in Genetics, Volume: 7
Swansea University Author: Ilyas Khan
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DOI (Published version): 10.3389/fgene.2016.00213
Abstract
Current cell-based repair strategies have proven unsuccessful for treating cartilage defects and osteoarthritic lesions, consequently advances in innovative therapeutics are required and mesenchymal stem cell-based (MSC) therapies are an expanding area of investigation. MSCs are capable of different...
Published in: | Frontiers in Genetics |
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ISSN: | 1664-8021 |
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2016
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URI: | https://cronfa.swan.ac.uk/Record/cronfa31769 |
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2017-02-15T13:08:07.4874894 v2 31769 2017-01-26 Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair 2536d955ff70e7b77063a8efe9103161 0000-0002-3886-1987 Ilyas Khan Ilyas Khan true false 2017-01-26 MEDS Current cell-based repair strategies have proven unsuccessful for treating cartilage defects and osteoarthritic lesions, consequently advances in innovative therapeutics are required and mesenchymal stem cell-based (MSC) therapies are an expanding area of investigation. MSCs are capable of differentiating into multiple cell lineages and exerting paracrine effects. Due to their easy isolation, expansion, and low immunogenicity, MSCs are an attractive option for regenerative medicine for joint repair. Recent studies have identified several MSC tissue reservoirs including in adipose tissue, bone marrow, cartilage, periosteum, and muscle. MSCs isolated from these discrete tissue niches exhibit distinct biological activities, and have enhanced regenerative potentials for different tissue types. Each MSC type has advantages and disadvantages for cartilage repair and their use in a clinical setting is a balance between expediency and effectiveness. In this review we explore the challenges associated with cartilage repair and regeneration using MSC-based cell therapies and provide an overview of phenotype, biological activities, and functional properties for each MSC population. This paper also specifically explores the therapeutic potential of each type of MSC, particularly focusing on which cells are capable of producing stratified hyaline-like articular cartilage regeneration. Finally we highlight areas for future investigation. Given that patients present with a variety of problems it is unlikely that cartilage regeneration will be a simple “one size fits all,” but more likely an array of solutions that need to be applied systematically to achieve regeneration of a biomechanically competent repair tissue. Journal Article Frontiers in Genetics 7 1664-8021 20 12 2016 2016-12-20 10.3389/fgene.2016.00213 COLLEGE NANME Medical School COLLEGE CODE MEDS Swansea University 2017-02-15T13:08:07.4874894 2017-01-26T11:55:57.5459108 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Christopher R. Fellows 1 Csaba Matta 2 Roza Zakany 3 Ilyas Khan 0000-0002-3886-1987 4 Ali Mobasheri 5 0031769-15022017130526.pdf fgene.pdf 2017-02-15T13:05:26.6500000 Output 2506369 application/pdf Version of Record true 2016-12-20T00:00:00.0000000 This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) true eng |
title |
Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair |
spellingShingle |
Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair Ilyas Khan |
title_short |
Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair |
title_full |
Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair |
title_fullStr |
Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair |
title_full_unstemmed |
Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair |
title_sort |
Adipose, Bone Marrow and Synovial Joint-Derived Mesenchymal Stem Cells for Cartilage Repair |
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2536d955ff70e7b77063a8efe9103161 |
author_id_fullname_str_mv |
2536d955ff70e7b77063a8efe9103161_***_Ilyas Khan |
author |
Ilyas Khan |
author2 |
Christopher R. Fellows Csaba Matta Roza Zakany Ilyas Khan Ali Mobasheri |
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Frontiers in Genetics |
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10.3389/fgene.2016.00213 |
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Faculty of Medicine, Health and Life Sciences |
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description |
Current cell-based repair strategies have proven unsuccessful for treating cartilage defects and osteoarthritic lesions, consequently advances in innovative therapeutics are required and mesenchymal stem cell-based (MSC) therapies are an expanding area of investigation. MSCs are capable of differentiating into multiple cell lineages and exerting paracrine effects. Due to their easy isolation, expansion, and low immunogenicity, MSCs are an attractive option for regenerative medicine for joint repair. Recent studies have identified several MSC tissue reservoirs including in adipose tissue, bone marrow, cartilage, periosteum, and muscle. MSCs isolated from these discrete tissue niches exhibit distinct biological activities, and have enhanced regenerative potentials for different tissue types. Each MSC type has advantages and disadvantages for cartilage repair and their use in a clinical setting is a balance between expediency and effectiveness. In this review we explore the challenges associated with cartilage repair and regeneration using MSC-based cell therapies and provide an overview of phenotype, biological activities, and functional properties for each MSC population. This paper also specifically explores the therapeutic potential of each type of MSC, particularly focusing on which cells are capable of producing stratified hyaline-like articular cartilage regeneration. Finally we highlight areas for future investigation. Given that patients present with a variety of problems it is unlikely that cartilage regeneration will be a simple “one size fits all,” but more likely an array of solutions that need to be applied systematically to achieve regeneration of a biomechanically competent repair tissue. |
published_date |
2016-12-20T07:04:39Z |
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1821388129307721728 |
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11.047501 |