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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...

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Autores principales: Liu, Yanchang, Cheng, Wendan, Zhao, Yao, Gao, Liang, Chang, Yongyun, Tong, Zhicheng, Li, Huiwu, Jing, Juehua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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.
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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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