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Radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing
BACKGROUND: Shockwaves and mesenchymal stem cells (MSCs) have been widely accepted as useful tools for many orthopedic applications. However, the modulatory effects of shockwaves on MSCs remain controversial. In this study, we explored the influence of radial shockwaves on human bone marrow MSCs usi...
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/PMC5845163/ https://www.ncbi.nlm.nih.gov/pubmed/29523197 http://dx.doi.org/10.1186/s13287-018-0805-5 |
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author | Zhang, Hao Li, Zhong-Li Yang, Fei Zhang, Qiang Su, Xiang-Zheng Li, Ji Zhang, Ning Liu, Chun-Hui Mao, Ning Zhu, Heng |
author_facet | Zhang, Hao Li, Zhong-Li Yang, Fei Zhang, Qiang Su, Xiang-Zheng Li, Ji Zhang, Ning Liu, Chun-Hui Mao, Ning Zhu, Heng |
author_sort | Zhang, Hao |
collection | PubMed |
description | BACKGROUND: Shockwaves and mesenchymal stem cells (MSCs) have been widely accepted as useful tools for many orthopedic applications. However, the modulatory effects of shockwaves on MSCs remain controversial. In this study, we explored the influence of radial shockwaves on human bone marrow MSCs using a floating model in vitro and evaluated the healing effects of these cells on cartilage defects in vivo using a rabbit model. METHODS: MSCs were cultured in vitro, harvested, resuspended, and treated with various doses of radial shockwaves in a floating system. Cell proliferation was evaluated by growth kinetics and Cell Counting Kit-8 (CCK-8) assay. In addition, the cell cycle and apoptotic activity were analyzed by fluorescence activated cell sorting. To explore the “stemness” of MSCs, cell colony-forming tests and multidifferentiation assays were performed. We also examined the MSC subcellular structure using transmission electron microscopy and examined the healing effects of these cells on cartilage defects by pathological analyses. RESULTS: The results of growth kinetics and CCK-8 assays showed that radial shockwave treatment significantly promoted MSC proliferation. Enhanced cell growth was also reflected by an increase in the numbers of cells in the S phase and a decrease in the numbers of cells arrested in the G0/G1 phase in shockwave-treated MSCs. Unexpectedly, shockwaves caused a slight increase in MSC apoptosis rates. Furthermore, radial shockwaves promoted self-replicating activity of MSCs. Transmission electron microscopy revealed that MSCs were metabolically activated by shockwave treatment. In addition, radial shockwaves favored MSC osteogenic differentiation but inhibited adipogenic activity. Most importantly, MSCs pretreated by radial shockwaves exhibited an enhanced healing effect on cartilage defects in vivo. Compared with control groups, shockwave-treated MSCs combined with bio-scaffolds significantly improved histological scores of injured rabbit knees. CONCLUSIONS: In the present study, we found that radial shockwaves significantly promoted the proliferation and self-renewal of MSCs in vitro and safely accelerated the cartilage repair process in vivo, indicating favorable clinical outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0805-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5845163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58451632018-03-14 Radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing Zhang, Hao Li, Zhong-Li Yang, Fei Zhang, Qiang Su, Xiang-Zheng Li, Ji Zhang, Ning Liu, Chun-Hui Mao, Ning Zhu, Heng Stem Cell Res Ther Research BACKGROUND: Shockwaves and mesenchymal stem cells (MSCs) have been widely accepted as useful tools for many orthopedic applications. However, the modulatory effects of shockwaves on MSCs remain controversial. In this study, we explored the influence of radial shockwaves on human bone marrow MSCs using a floating model in vitro and evaluated the healing effects of these cells on cartilage defects in vivo using a rabbit model. METHODS: MSCs were cultured in vitro, harvested, resuspended, and treated with various doses of radial shockwaves in a floating system. Cell proliferation was evaluated by growth kinetics and Cell Counting Kit-8 (CCK-8) assay. In addition, the cell cycle and apoptotic activity were analyzed by fluorescence activated cell sorting. To explore the “stemness” of MSCs, cell colony-forming tests and multidifferentiation assays were performed. We also examined the MSC subcellular structure using transmission electron microscopy and examined the healing effects of these cells on cartilage defects by pathological analyses. RESULTS: The results of growth kinetics and CCK-8 assays showed that radial shockwave treatment significantly promoted MSC proliferation. Enhanced cell growth was also reflected by an increase in the numbers of cells in the S phase and a decrease in the numbers of cells arrested in the G0/G1 phase in shockwave-treated MSCs. Unexpectedly, shockwaves caused a slight increase in MSC apoptosis rates. Furthermore, radial shockwaves promoted self-replicating activity of MSCs. Transmission electron microscopy revealed that MSCs were metabolically activated by shockwave treatment. In addition, radial shockwaves favored MSC osteogenic differentiation but inhibited adipogenic activity. Most importantly, MSCs pretreated by radial shockwaves exhibited an enhanced healing effect on cartilage defects in vivo. Compared with control groups, shockwave-treated MSCs combined with bio-scaffolds significantly improved histological scores of injured rabbit knees. CONCLUSIONS: In the present study, we found that radial shockwaves significantly promoted the proliferation and self-renewal of MSCs in vitro and safely accelerated the cartilage repair process in vivo, indicating favorable clinical outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0805-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-09 /pmc/articles/PMC5845163/ /pubmed/29523197 http://dx.doi.org/10.1186/s13287-018-0805-5 Text en © The Author(s). 2018 Open AccessThis 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 Zhang, Hao Li, Zhong-Li Yang, Fei Zhang, Qiang Su, Xiang-Zheng Li, Ji Zhang, Ning Liu, Chun-Hui Mao, Ning Zhu, Heng Radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing |
title | Radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing |
title_full | Radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing |
title_fullStr | Radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing |
title_full_unstemmed | Radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing |
title_short | Radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing |
title_sort | radial shockwave treatment promotes human mesenchymal stem cell self-renewal and enhances cartilage healing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845163/ https://www.ncbi.nlm.nih.gov/pubmed/29523197 http://dx.doi.org/10.1186/s13287-018-0805-5 |
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