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Excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm
Night shift workers with disordered rhythmic mechanical loading are more prone to intervertebral disc degeneration (IDD). Our results showed that circadian rhythm (CR) was dampened in degenerated and aged NP cells. Long-term environmental CR disruption promoted IDD in rats. Excessive mechanical stra...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741925/ https://www.ncbi.nlm.nih.gov/pubmed/34934193 http://dx.doi.org/10.1038/s12276-021-00716-6 |
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author | Ding, Sheng-Long Zhang, Tai-Wei Zhang, Qi-Chen Ding, Wang Li, Ze-Fang Han, Guan-Jie Bai, Jin-Song Li, Xi-Lei Dong, Jian Wang, Hui-Ren Jiang, Li-Bo |
author_facet | Ding, Sheng-Long Zhang, Tai-Wei Zhang, Qi-Chen Ding, Wang Li, Ze-Fang Han, Guan-Jie Bai, Jin-Song Li, Xi-Lei Dong, Jian Wang, Hui-Ren Jiang, Li-Bo |
author_sort | Ding, Sheng-Long |
collection | PubMed |
description | Night shift workers with disordered rhythmic mechanical loading are more prone to intervertebral disc degeneration (IDD). Our results showed that circadian rhythm (CR) was dampened in degenerated and aged NP cells. Long-term environmental CR disruption promoted IDD in rats. Excessive mechanical strain disrupted the CR and inhibited the expression of core clock proteins. The inhibitory effect of mechanical loading on the expression of extracellular matrix genes could be reversed by BMAL1 overexpression in NP cells. The Rho/ROCK pathway was demonstrated to mediate the effect of mechanical stimulation on CR. Prolonged mechanical loading for 12 months affected intrinsic CR genes and induced IDD in a model of upright posture in a normal environment. Unexpectedly, mechanical loading further accelerated the IDD in an Light-Dark (LD) cycle-disrupted environment. These results indicated that intrinsic CR disruption might be a mechanism involved in overloading-induced IDD and a potential drug target for night shift workers. |
format | Online Article Text |
id | pubmed-8741925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87419252022-01-20 Excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm Ding, Sheng-Long Zhang, Tai-Wei Zhang, Qi-Chen Ding, Wang Li, Ze-Fang Han, Guan-Jie Bai, Jin-Song Li, Xi-Lei Dong, Jian Wang, Hui-Ren Jiang, Li-Bo Exp Mol Med Article Night shift workers with disordered rhythmic mechanical loading are more prone to intervertebral disc degeneration (IDD). Our results showed that circadian rhythm (CR) was dampened in degenerated and aged NP cells. Long-term environmental CR disruption promoted IDD in rats. Excessive mechanical strain disrupted the CR and inhibited the expression of core clock proteins. The inhibitory effect of mechanical loading on the expression of extracellular matrix genes could be reversed by BMAL1 overexpression in NP cells. The Rho/ROCK pathway was demonstrated to mediate the effect of mechanical stimulation on CR. Prolonged mechanical loading for 12 months affected intrinsic CR genes and induced IDD in a model of upright posture in a normal environment. Unexpectedly, mechanical loading further accelerated the IDD in an Light-Dark (LD) cycle-disrupted environment. These results indicated that intrinsic CR disruption might be a mechanism involved in overloading-induced IDD and a potential drug target for night shift workers. Nature Publishing Group UK 2021-12-21 /pmc/articles/PMC8741925/ /pubmed/34934193 http://dx.doi.org/10.1038/s12276-021-00716-6 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ding, Sheng-Long Zhang, Tai-Wei Zhang, Qi-Chen Ding, Wang Li, Ze-Fang Han, Guan-Jie Bai, Jin-Song Li, Xi-Lei Dong, Jian Wang, Hui-Ren Jiang, Li-Bo Excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm |
title | Excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm |
title_full | Excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm |
title_fullStr | Excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm |
title_full_unstemmed | Excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm |
title_short | Excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm |
title_sort | excessive mechanical strain accelerates intervertebral disc degeneration by disrupting intrinsic circadian rhythm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741925/ https://www.ncbi.nlm.nih.gov/pubmed/34934193 http://dx.doi.org/10.1038/s12276-021-00716-6 |
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