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Cyclic Mechanical Strain Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through GCN5 and Wnt/β-Catenin
Bone marrow mesenchymal stem cells (BMSCs) play a critical role in bone formation and are extremely sensitive to external mechanical stimuli. Mechanical signals can regulate the biological behavior of cells on the surface of titanium-related prostheses and inducing osteogenic differentiation of BMSC...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634263/ https://www.ncbi.nlm.nih.gov/pubmed/34869255 http://dx.doi.org/10.3389/fbioe.2021.735949 |
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author | Liu, Yanchang Cheng, Wendan Zhao, Yao Gao, Liang Chang, Yongyun Tong, Zhicheng Li, Huiwu Jing, Juehua |
author_facet | Liu, Yanchang Cheng, Wendan Zhao, Yao Gao, Liang Chang, Yongyun Tong, Zhicheng Li, Huiwu Jing, Juehua |
author_sort | Liu, Yanchang |
collection | PubMed |
description | Bone marrow mesenchymal stem cells (BMSCs) play a critical role in bone formation and are extremely sensitive to external mechanical stimuli. Mechanical signals can regulate the biological behavior of cells on the surface of titanium-related prostheses and inducing osteogenic differentiation of BMSCs, which provides the integration of host bone and prosthesis benefits. But the mechanism is still unclear. In this study, BMSCs planted on the surface of TiO(2) nanotubes were subjected to cyclic mechanical stress, and the related mechanisms were explored. The results of alkaline phosphatase staining, real-time PCR, and Western blot showed that cyclic mechanical stress can regulate the expression level of osteogenic differentiation markers in BMSCs on the surface of TiO(2) nanotubes through Wnt/β-catenin. As an important member of the histone acetyltransferase family, GCN5 exerted regulatory effects on receiving mechanical signals. The results of the ChIP assay indicated that GCN5 could activate the Wnt promoter region. Hence, we concluded that the osteogenic differentiation ability of BMSCs on the surface of TiO(2) nanotubes was enhanced under the stimulation of cyclic mechanical stress, and GCN5 mediated this process through Wnt/β-catenin. |
format | Online Article Text |
id | pubmed-8634263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86342632021-12-02 Cyclic Mechanical Strain Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through GCN5 and Wnt/β-Catenin Liu, Yanchang Cheng, Wendan Zhao, Yao Gao, Liang Chang, Yongyun Tong, Zhicheng Li, Huiwu Jing, Juehua Front Bioeng Biotechnol Bioengineering and Biotechnology Bone marrow mesenchymal stem cells (BMSCs) play a critical role in bone formation and are extremely sensitive to external mechanical stimuli. Mechanical signals can regulate the biological behavior of cells on the surface of titanium-related prostheses and inducing osteogenic differentiation of BMSCs, which provides the integration of host bone and prosthesis benefits. But the mechanism is still unclear. In this study, BMSCs planted on the surface of TiO(2) nanotubes were subjected to cyclic mechanical stress, and the related mechanisms were explored. The results of alkaline phosphatase staining, real-time PCR, and Western blot showed that cyclic mechanical stress can regulate the expression level of osteogenic differentiation markers in BMSCs on the surface of TiO(2) nanotubes through Wnt/β-catenin. As an important member of the histone acetyltransferase family, GCN5 exerted regulatory effects on receiving mechanical signals. The results of the ChIP assay indicated that GCN5 could activate the Wnt promoter region. Hence, we concluded that the osteogenic differentiation ability of BMSCs on the surface of TiO(2) nanotubes was enhanced under the stimulation of cyclic mechanical stress, and GCN5 mediated this process through Wnt/β-catenin. Frontiers Media S.A. 2021-11-15 /pmc/articles/PMC8634263/ /pubmed/34869255 http://dx.doi.org/10.3389/fbioe.2021.735949 Text en Copyright © 2021 Liu, Cheng, Zhao, Gao, Chang, Tong, Li and Jing. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Liu, Yanchang Cheng, Wendan Zhao, Yao Gao, Liang Chang, Yongyun Tong, Zhicheng Li, Huiwu Jing, Juehua Cyclic Mechanical Strain Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through GCN5 and Wnt/β-Catenin |
title | Cyclic Mechanical Strain Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through GCN5 and Wnt/β-Catenin |
title_full | Cyclic Mechanical Strain Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through GCN5 and Wnt/β-Catenin |
title_fullStr | Cyclic Mechanical Strain Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through GCN5 and Wnt/β-Catenin |
title_full_unstemmed | Cyclic Mechanical Strain Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through GCN5 and Wnt/β-Catenin |
title_short | Cyclic Mechanical Strain Regulates Osteoblastic Differentiation of Mesenchymal Stem Cells on TiO(2) Nanotubes Through GCN5 and Wnt/β-Catenin |
title_sort | cyclic mechanical strain regulates osteoblastic differentiation of mesenchymal stem cells on tio(2) nanotubes through gcn5 and wnt/β-catenin |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634263/ https://www.ncbi.nlm.nih.gov/pubmed/34869255 http://dx.doi.org/10.3389/fbioe.2021.735949 |
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