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Cell sources proposed for nucleus pulposus regeneration
Lower back pain (LBP) occurs in 80% of adults in their lifetime; resulting in LBP being one of the biggest causes of disability worldwide. Chronic LBP has been linked to the degeneration of the intervertebral disc (IVD). The current treatments for chronic back pain only provide alleviation of sympto...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8717099/ https://www.ncbi.nlm.nih.gov/pubmed/35005441 http://dx.doi.org/10.1002/jsp2.1175 |
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author | Williams, Rebecca J. Tryfonidou, Marianna A. Snuggs, Joseph Wiliam Le Maitre, Christine Lyn |
author_facet | Williams, Rebecca J. Tryfonidou, Marianna A. Snuggs, Joseph Wiliam Le Maitre, Christine Lyn |
author_sort | Williams, Rebecca J. |
collection | PubMed |
description | Lower back pain (LBP) occurs in 80% of adults in their lifetime; resulting in LBP being one of the biggest causes of disability worldwide. Chronic LBP has been linked to the degeneration of the intervertebral disc (IVD). The current treatments for chronic back pain only provide alleviation of symptoms through pain relief, tissue removal, or spinal fusion; none of which target regenerating the degenerate IVD. As nucleus pulposus (NP) degeneration is thought to represent a key initiation site of IVD degeneration, cell therapy that specifically targets the restoration of the NP has been reviewed here. A literature search to quantitatively assess all cell types used in NP regeneration was undertaken. With key cell sources: NP cells; annulus fibrosus cells; notochordal cells; chondrocytes; bone marrow mesenchymal stromal cells; adipose‐derived stromal cells; and induced pluripotent stem cells extensively analyzed for their regenerative potential of the NP. This review highlights: accessibility; expansion capability in vitro; cell survival in an IVD environment; regenerative potential; and safety for these key potential cell sources. In conclusion, while several potential cell sources have been proposed, iPSC may provide the most promising regenerative potential. |
format | Online Article Text |
id | pubmed-8717099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87170992022-01-06 Cell sources proposed for nucleus pulposus regeneration Williams, Rebecca J. Tryfonidou, Marianna A. Snuggs, Joseph Wiliam Le Maitre, Christine Lyn JOR Spine Reviews Lower back pain (LBP) occurs in 80% of adults in their lifetime; resulting in LBP being one of the biggest causes of disability worldwide. Chronic LBP has been linked to the degeneration of the intervertebral disc (IVD). The current treatments for chronic back pain only provide alleviation of symptoms through pain relief, tissue removal, or spinal fusion; none of which target regenerating the degenerate IVD. As nucleus pulposus (NP) degeneration is thought to represent a key initiation site of IVD degeneration, cell therapy that specifically targets the restoration of the NP has been reviewed here. A literature search to quantitatively assess all cell types used in NP regeneration was undertaken. With key cell sources: NP cells; annulus fibrosus cells; notochordal cells; chondrocytes; bone marrow mesenchymal stromal cells; adipose‐derived stromal cells; and induced pluripotent stem cells extensively analyzed for their regenerative potential of the NP. This review highlights: accessibility; expansion capability in vitro; cell survival in an IVD environment; regenerative potential; and safety for these key potential cell sources. In conclusion, while several potential cell sources have been proposed, iPSC may provide the most promising regenerative potential. John Wiley & Sons, Inc. 2021-11-24 /pmc/articles/PMC8717099/ /pubmed/35005441 http://dx.doi.org/10.1002/jsp2.1175 Text en © 2021 The Authors. JOR Spine published by Wiley Periodicals LLC on behalf of Orthopaedic Research Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Reviews Williams, Rebecca J. Tryfonidou, Marianna A. Snuggs, Joseph Wiliam Le Maitre, Christine Lyn Cell sources proposed for nucleus pulposus regeneration |
title | Cell sources proposed for nucleus pulposus regeneration |
title_full | Cell sources proposed for nucleus pulposus regeneration |
title_fullStr | Cell sources proposed for nucleus pulposus regeneration |
title_full_unstemmed | Cell sources proposed for nucleus pulposus regeneration |
title_short | Cell sources proposed for nucleus pulposus regeneration |
title_sort | cell sources proposed for nucleus pulposus regeneration |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8717099/ https://www.ncbi.nlm.nih.gov/pubmed/35005441 http://dx.doi.org/10.1002/jsp2.1175 |
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