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Effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells
BACKGROUND: Uniaxial/biaxial tensile stress has been employed to induce chondrocyte differentiation of mesenchymal stem cells. However, the effects of radial tensile stimuli on differentiation of MSCs into fibrocartilage remain unclear. RESULTS: It was found that induced bone marrow mesenchymal stem...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003351/ https://www.ncbi.nlm.nih.gov/pubmed/32024525 http://dx.doi.org/10.1186/s12938-020-0751-1 |
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author | Su, Xuelian Wang, Jizeng Kang, Hong Bao, Guangjie Liu, Lin |
author_facet | Su, Xuelian Wang, Jizeng Kang, Hong Bao, Guangjie Liu, Lin |
author_sort | Su, Xuelian |
collection | PubMed |
description | BACKGROUND: Uniaxial/biaxial tensile stress has been employed to induce chondrocyte differentiation of mesenchymal stem cells. However, the effects of radial tensile stimuli on differentiation of MSCs into fibrocartilage remain unclear. RESULTS: It was found that induced bone marrow mesenchymal stem cells (BMSCs) were not only similar to TMJ disc cells in morphology, but also could synthesize type I collagen (Col I), a small amount of type II collagen (Col II) and glycosaminoglycans (GAGs). The synthesis of Col I significantly increased while that of Col II gradually decreased with increasing tensile strength. The ratio of Col I to Col II was 1.8 to 1 and 2 to 1 in the 10% and 15% stretching groups, respectively. The gene expression of Col I and GAGs was significantly upregulated, whereas that of Col II was downregulated. However, the higher tensile stimulation (15%) promoted the synthesis of α-smooth muscle actin (α-SMA). Too much α-SMA is not conducive to constructing engineered tissue. CONCLUSION: Therefore, the 10% radial tensile stimulus was the optimal strength for inducing the BMSCs to differentiate into fibrochondrocytes of the temporomandibular joint (TMJ) disc. This work provided a novel approach for inducing BMSCs to differentiate into fibrochondrocytes. |
format | Online Article Text |
id | pubmed-7003351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70033512020-02-10 Effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells Su, Xuelian Wang, Jizeng Kang, Hong Bao, Guangjie Liu, Lin Biomed Eng Online Research BACKGROUND: Uniaxial/biaxial tensile stress has been employed to induce chondrocyte differentiation of mesenchymal stem cells. However, the effects of radial tensile stimuli on differentiation of MSCs into fibrocartilage remain unclear. RESULTS: It was found that induced bone marrow mesenchymal stem cells (BMSCs) were not only similar to TMJ disc cells in morphology, but also could synthesize type I collagen (Col I), a small amount of type II collagen (Col II) and glycosaminoglycans (GAGs). The synthesis of Col I significantly increased while that of Col II gradually decreased with increasing tensile strength. The ratio of Col I to Col II was 1.8 to 1 and 2 to 1 in the 10% and 15% stretching groups, respectively. The gene expression of Col I and GAGs was significantly upregulated, whereas that of Col II was downregulated. However, the higher tensile stimulation (15%) promoted the synthesis of α-smooth muscle actin (α-SMA). Too much α-SMA is not conducive to constructing engineered tissue. CONCLUSION: Therefore, the 10% radial tensile stimulus was the optimal strength for inducing the BMSCs to differentiate into fibrochondrocytes of the temporomandibular joint (TMJ) disc. This work provided a novel approach for inducing BMSCs to differentiate into fibrochondrocytes. BioMed Central 2020-02-05 /pmc/articles/PMC7003351/ /pubmed/32024525 http://dx.doi.org/10.1186/s12938-020-0751-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Su, Xuelian Wang, Jizeng Kang, Hong Bao, Guangjie Liu, Lin Effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells |
title | Effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells |
title_full | Effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells |
title_fullStr | Effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells |
title_full_unstemmed | Effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells |
title_short | Effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells |
title_sort | effects of dynamic radial tensile stress on fibrocartilage differentiation of bone marrow mesenchymal stem cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003351/ https://www.ncbi.nlm.nih.gov/pubmed/32024525 http://dx.doi.org/10.1186/s12938-020-0751-1 |
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