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Integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ECM formation promoted by mechanical tensile strain

BACKGROUND: Mechanical strain plays a great role in growth and differentiation of osteoblast. A previous study indicated that integrin-β (β1, β5) mediated osteoblast proliferation promoted by mechanical tensile strain. However, the involvement of integrin-β in osteoblastic differentiation and extrac...

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Autores principales: Zeng, Qiangcheng, Guo, Yong, Liu, Yongming, Li, Ruixin, Zhang, Xinchang, Liu, Lu, Wang, Yang, Zhang, Xizheng, Zou, Xianqiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436743/
https://www.ncbi.nlm.nih.gov/pubmed/25971622
http://dx.doi.org/10.1186/s40659-015-0014-y
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author Zeng, Qiangcheng
Guo, Yong
Liu, Yongming
Li, Ruixin
Zhang, Xinchang
Liu, Lu
Wang, Yang
Zhang, Xizheng
Zou, Xianqiong
author_facet Zeng, Qiangcheng
Guo, Yong
Liu, Yongming
Li, Ruixin
Zhang, Xinchang
Liu, Lu
Wang, Yang
Zhang, Xizheng
Zou, Xianqiong
author_sort Zeng, Qiangcheng
collection PubMed
description BACKGROUND: Mechanical strain plays a great role in growth and differentiation of osteoblast. A previous study indicated that integrin-β (β1, β5) mediated osteoblast proliferation promoted by mechanical tensile strain. However, the involvement of integrin-β in osteoblastic differentiation and extracellular matrix (ECM) formation induced by mechanical tensile strain, remains unclear. RESULTS: After transfection with integrin-β1 siRNA or integrin-β5 siRNA, mouse MC3T3-E1 preosteoblasts were cultured in cell culture dishes and stimulated with mechanical tensile strain of 2500 microstrain (με) at 0.5 Hz applied once a day for 1 h over 3 or 5 consecutive days. The cyclic tensile strain promoted osteoblastic differentiation of MC3T3-E1 cells. Transfection with integrin-β1 siRNA attenuated the osteoblastic diffenentiation induced by the tensile strain. By contrast, transfection with integrin-β5 siRNA had little effect on the osteoblastic differentiation induced by the strain. At the same time, the result of ECM formation promoted by the strain, was similar to the osteoblastic differentiation. CONCLUSION: Integrin-β1 mediates osteoblast differentiation and osteoblastic ECM formation promoted by cyclic tensile strain, and integrin-β5 is not involved in the osteoblasts response to the tensile strain. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40659-015-0014-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-44367432015-05-20 Integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ECM formation promoted by mechanical tensile strain Zeng, Qiangcheng Guo, Yong Liu, Yongming Li, Ruixin Zhang, Xinchang Liu, Lu Wang, Yang Zhang, Xizheng Zou, Xianqiong Biol Res Research Article BACKGROUND: Mechanical strain plays a great role in growth and differentiation of osteoblast. A previous study indicated that integrin-β (β1, β5) mediated osteoblast proliferation promoted by mechanical tensile strain. However, the involvement of integrin-β in osteoblastic differentiation and extracellular matrix (ECM) formation induced by mechanical tensile strain, remains unclear. RESULTS: After transfection with integrin-β1 siRNA or integrin-β5 siRNA, mouse MC3T3-E1 preosteoblasts were cultured in cell culture dishes and stimulated with mechanical tensile strain of 2500 microstrain (με) at 0.5 Hz applied once a day for 1 h over 3 or 5 consecutive days. The cyclic tensile strain promoted osteoblastic differentiation of MC3T3-E1 cells. Transfection with integrin-β1 siRNA attenuated the osteoblastic diffenentiation induced by the tensile strain. By contrast, transfection with integrin-β5 siRNA had little effect on the osteoblastic differentiation induced by the strain. At the same time, the result of ECM formation promoted by the strain, was similar to the osteoblastic differentiation. CONCLUSION: Integrin-β1 mediates osteoblast differentiation and osteoblastic ECM formation promoted by cyclic tensile strain, and integrin-β5 is not involved in the osteoblasts response to the tensile strain. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40659-015-0014-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-14 /pmc/articles/PMC4436743/ /pubmed/25971622 http://dx.doi.org/10.1186/s40659-015-0014-y Text en © Zeng et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Zeng, Qiangcheng
Guo, Yong
Liu, Yongming
Li, Ruixin
Zhang, Xinchang
Liu, Lu
Wang, Yang
Zhang, Xizheng
Zou, Xianqiong
Integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ECM formation promoted by mechanical tensile strain
title Integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ECM formation promoted by mechanical tensile strain
title_full Integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ECM formation promoted by mechanical tensile strain
title_fullStr Integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ECM formation promoted by mechanical tensile strain
title_full_unstemmed Integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ECM formation promoted by mechanical tensile strain
title_short Integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ECM formation promoted by mechanical tensile strain
title_sort integrin-β1, not integrin-β5, mediates osteoblastic differentiation and ecm formation promoted by mechanical tensile strain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436743/
https://www.ncbi.nlm.nih.gov/pubmed/25971622
http://dx.doi.org/10.1186/s40659-015-0014-y
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