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Discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model
A multitude of studies has indicated the potential of cell therapy as a method for intervertebral disc (IVD) regeneration. Transplantation of a variety of cells has been assessed and shown capable of deterring the rate of degeneration in animal models and in human clinical trials. In this study, a n...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686803/ https://www.ncbi.nlm.nih.gov/pubmed/31463441 http://dx.doi.org/10.1002/jsp2.1013 |
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author | Hiraishi, Syunsuke Schol, Jordy Sakai, Daisuke Nukaga, Tadashi Erickson, Isaac Silverman, Lara Foley, Kevin Watanabe, Masahiko |
author_facet | Hiraishi, Syunsuke Schol, Jordy Sakai, Daisuke Nukaga, Tadashi Erickson, Isaac Silverman, Lara Foley, Kevin Watanabe, Masahiko |
author_sort | Hiraishi, Syunsuke |
collection | PubMed |
description | A multitude of studies has indicated the potential of cell therapy as a method for intervertebral disc (IVD) regeneration. Transplantation of a variety of cells has been assessed and shown capable of deterring the rate of degeneration in animal models and in human clinical trials. In this study, a novel approach using human discogenic nucleus pulposus cells directly from their cryopreserved state was assessed. In an established canine disc degeneration model, the degeneration process was evaluated in IVDs receiving precultured discogenic cells, thawed‐only discogenic cells, and a saline sham injection after induction of degeneration. Degeneration progression was followed over time by the evaluation of the disc height index (DHI). Finally, after 12 weeks, the manipulated and control discs were explanted, histologically stained, and scored. Treated discs demonstrated retained DHI values for all treatment options. Histologic evaluations demonstrated significant improvement of matrix features compared to the sham. Moreover, thawed‐only cells function at least as well as precultured discogenic cells. In short, cell transplantation of human discogenic cells directly from their cryopreserved state can arrest disc height degeneration and maintain histological matrix features in a canine disc degeneration model. The presented work demonstrates the potential of an off‐the‐shelf cell therapy product to treat degenerative disc disease. |
format | Online Article Text |
id | pubmed-6686803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66868032019-08-28 Discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model Hiraishi, Syunsuke Schol, Jordy Sakai, Daisuke Nukaga, Tadashi Erickson, Isaac Silverman, Lara Foley, Kevin Watanabe, Masahiko JOR Spine Research Articles A multitude of studies has indicated the potential of cell therapy as a method for intervertebral disc (IVD) regeneration. Transplantation of a variety of cells has been assessed and shown capable of deterring the rate of degeneration in animal models and in human clinical trials. In this study, a novel approach using human discogenic nucleus pulposus cells directly from their cryopreserved state was assessed. In an established canine disc degeneration model, the degeneration process was evaluated in IVDs receiving precultured discogenic cells, thawed‐only discogenic cells, and a saline sham injection after induction of degeneration. Degeneration progression was followed over time by the evaluation of the disc height index (DHI). Finally, after 12 weeks, the manipulated and control discs were explanted, histologically stained, and scored. Treated discs demonstrated retained DHI values for all treatment options. Histologic evaluations demonstrated significant improvement of matrix features compared to the sham. Moreover, thawed‐only cells function at least as well as precultured discogenic cells. In short, cell transplantation of human discogenic cells directly from their cryopreserved state can arrest disc height degeneration and maintain histological matrix features in a canine disc degeneration model. The presented work demonstrates the potential of an off‐the‐shelf cell therapy product to treat degenerative disc disease. John Wiley & Sons, Inc. 2018-05-11 /pmc/articles/PMC6686803/ /pubmed/31463441 http://dx.doi.org/10.1002/jsp2.1013 Text en © 2018 The Authors. JOR Spine published by Wiley Periodicals, Inc. on behalf of Orthopaedic Research Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Hiraishi, Syunsuke Schol, Jordy Sakai, Daisuke Nukaga, Tadashi Erickson, Isaac Silverman, Lara Foley, Kevin Watanabe, Masahiko Discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model |
title | Discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model |
title_full | Discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model |
title_fullStr | Discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model |
title_full_unstemmed | Discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model |
title_short | Discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model |
title_sort | discogenic cell transplantation directly from a cryopreserved state in an induced intervertebral disc degeneration canine model |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686803/ https://www.ncbi.nlm.nih.gov/pubmed/31463441 http://dx.doi.org/10.1002/jsp2.1013 |
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