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A comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells
Tendon is a commonly injured soft musculoskeletal tissue, however, poor healing potential and ineffective treatment strategies result in persistent injuries and tissue that is unable to perform its normal physiological function. The identification of a stem cell population within tendon tissue holds...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897930/ https://www.ncbi.nlm.nih.gov/pubmed/29650048 http://dx.doi.org/10.1186/s12891-018-2038-2 |
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author | Lee, Katie Joanna Clegg, Peter David Comerford, Eithne Josephine Canty-Laird, Elizabeth Gail |
author_facet | Lee, Katie Joanna Clegg, Peter David Comerford, Eithne Josephine Canty-Laird, Elizabeth Gail |
author_sort | Lee, Katie Joanna |
collection | PubMed |
description | Tendon is a commonly injured soft musculoskeletal tissue, however, poor healing potential and ineffective treatment strategies result in persistent injuries and tissue that is unable to perform its normal physiological function. The identification of a stem cell population within tendon tissue holds therapeutic potential for treatment of tendon injuries. This study aimed, for the first time, to characterise and compare tenocyte and tendon-derived stem cell (TDSC) populations in murine tendon. Tenocytes and TDSCs were isolated from murine tail tendon. The cells were characterised for morphology, clonogenicity, proliferation, stem cell and tenogenic marker expression and multipotency. TDSCs demonstrated a rounded morphology, compared with a more fibroblastic morphology for tenocytes. Tenocytes had greater clonogenic potential and a smaller population doubling time compared with TDSCs. Stem cell and early tenogenic markers were more highly expressed in TDSCs, whereas late tenogenic markers were more highly expressed in tenocytes. Multipotency was increased in TDSCs with the presence of adipogenic differentiation which was absent in tenocytes. The differences in morphology, clonogenicity, stem cell marker expression and multipotency observed between tenocytes and TDSCs indicate that at least two cell populations are present in murine tail tendon. Determination of the most effective cell population for tendon repair is required in future studies, which in turn may aid in tendon repair strategies. |
format | Online Article Text |
id | pubmed-5897930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58979302018-04-20 A comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells Lee, Katie Joanna Clegg, Peter David Comerford, Eithne Josephine Canty-Laird, Elizabeth Gail BMC Musculoskelet Disord Research Article Tendon is a commonly injured soft musculoskeletal tissue, however, poor healing potential and ineffective treatment strategies result in persistent injuries and tissue that is unable to perform its normal physiological function. The identification of a stem cell population within tendon tissue holds therapeutic potential for treatment of tendon injuries. This study aimed, for the first time, to characterise and compare tenocyte and tendon-derived stem cell (TDSC) populations in murine tendon. Tenocytes and TDSCs were isolated from murine tail tendon. The cells were characterised for morphology, clonogenicity, proliferation, stem cell and tenogenic marker expression and multipotency. TDSCs demonstrated a rounded morphology, compared with a more fibroblastic morphology for tenocytes. Tenocytes had greater clonogenic potential and a smaller population doubling time compared with TDSCs. Stem cell and early tenogenic markers were more highly expressed in TDSCs, whereas late tenogenic markers were more highly expressed in tenocytes. Multipotency was increased in TDSCs with the presence of adipogenic differentiation which was absent in tenocytes. The differences in morphology, clonogenicity, stem cell marker expression and multipotency observed between tenocytes and TDSCs indicate that at least two cell populations are present in murine tail tendon. Determination of the most effective cell population for tendon repair is required in future studies, which in turn may aid in tendon repair strategies. BioMed Central 2018-04-12 /pmc/articles/PMC5897930/ /pubmed/29650048 http://dx.doi.org/10.1186/s12891-018-2038-2 Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lee, Katie Joanna Clegg, Peter David Comerford, Eithne Josephine Canty-Laird, Elizabeth Gail A comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells |
title | A comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells |
title_full | A comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells |
title_fullStr | A comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells |
title_full_unstemmed | A comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells |
title_short | A comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells |
title_sort | comparison of the stem cell characteristics of murine tenocytes and tendon-derived stem cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897930/ https://www.ncbi.nlm.nih.gov/pubmed/29650048 http://dx.doi.org/10.1186/s12891-018-2038-2 |
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