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Extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy
Background: Mechanical load contributes a lot to the initiation and progression of disc degeneration. Annulus fibrosus (AF) cell biology under mechanical tension remains largely unclear. Objective: The present study was aimed to investigate AF cell senescence under mechanical tension and the potenti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470409/ https://www.ncbi.nlm.nih.gov/pubmed/30910846 http://dx.doi.org/10.1042/BSR20190163 |
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author | Zhao, Liang Tian, Baofang Xu, Qing Zhang, Cunxin Zhang, Luo Fang, Haolin |
author_facet | Zhao, Liang Tian, Baofang Xu, Qing Zhang, Cunxin Zhang, Luo Fang, Haolin |
author_sort | Zhao, Liang |
collection | PubMed |
description | Background: Mechanical load contributes a lot to the initiation and progression of disc degeneration. Annulus fibrosus (AF) cell biology under mechanical tension remains largely unclear. Objective: The present study was aimed to investigate AF cell senescence under mechanical tension and the potential role of autophagy. Methods: Rat AF cells were cultured and experienced different magnitudes (5% elongation and 20% elongation) of mechanical tension for 12 days. Control AF cells were kept static. Cell proliferation, telomerase activity, cell cycle fraction, and expression of senescence-related molecules (p16 and p53) and matrix macromolecules (aggrecan and collagen I) were analyzed to evaluate cell senescence. In addition, expression of Beclin-1 and LC3, and the ratio of LC3-II to LC3-I were analyzed to investigate cell autophagy. Results: Compared with the control group and 5% tension group, 20% tension group significantly decreased cell proliferation potency and telomerase activity, increased G1/G0 phase fraction, and up-regulated gene/protein expression of p16 and p53, whereas down-regulated gene/protein expression of aggrecan and collagen I. In addition, autophagy-related parameters such as gene/protein expression of Beclin-1 and LC3, and the ratio of LC3-II to LC3-I, were obviously suppressed in the 20% tension group. Conclusion: High mechanical tension promotes AF cell senescence though suppressing cellular autophagy. The present study will help us to better understand AF cell biology under mechanical tension and mechanical load-related disc degeneration. |
format | Online Article Text |
id | pubmed-6470409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64704092019-04-26 Extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy Zhao, Liang Tian, Baofang Xu, Qing Zhang, Cunxin Zhang, Luo Fang, Haolin Biosci Rep Research Articles Background: Mechanical load contributes a lot to the initiation and progression of disc degeneration. Annulus fibrosus (AF) cell biology under mechanical tension remains largely unclear. Objective: The present study was aimed to investigate AF cell senescence under mechanical tension and the potential role of autophagy. Methods: Rat AF cells were cultured and experienced different magnitudes (5% elongation and 20% elongation) of mechanical tension for 12 days. Control AF cells were kept static. Cell proliferation, telomerase activity, cell cycle fraction, and expression of senescence-related molecules (p16 and p53) and matrix macromolecules (aggrecan and collagen I) were analyzed to evaluate cell senescence. In addition, expression of Beclin-1 and LC3, and the ratio of LC3-II to LC3-I were analyzed to investigate cell autophagy. Results: Compared with the control group and 5% tension group, 20% tension group significantly decreased cell proliferation potency and telomerase activity, increased G1/G0 phase fraction, and up-regulated gene/protein expression of p16 and p53, whereas down-regulated gene/protein expression of aggrecan and collagen I. In addition, autophagy-related parameters such as gene/protein expression of Beclin-1 and LC3, and the ratio of LC3-II to LC3-I, were obviously suppressed in the 20% tension group. Conclusion: High mechanical tension promotes AF cell senescence though suppressing cellular autophagy. The present study will help us to better understand AF cell biology under mechanical tension and mechanical load-related disc degeneration. Portland Press Ltd. 2019-04-17 /pmc/articles/PMC6470409/ /pubmed/30910846 http://dx.doi.org/10.1042/BSR20190163 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Articles Zhao, Liang Tian, Baofang Xu, Qing Zhang, Cunxin Zhang, Luo Fang, Haolin Extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy |
title | Extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy |
title_full | Extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy |
title_fullStr | Extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy |
title_full_unstemmed | Extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy |
title_short | Extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy |
title_sort | extensive mechanical tension promotes annulus fibrosus cell senescence through suppressing cellular autophagy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470409/ https://www.ncbi.nlm.nih.gov/pubmed/30910846 http://dx.doi.org/10.1042/BSR20190163 |
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