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Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway

BACKGROUND: Intervertebral disc is responsible for absorbing and transmitting mechanical compression. Under physiological conditions, the peripheral annulus fibrosus (AF) cells are subjected to different magnitudes of transverse mechanical stretch depending on the swelling of the central nucleus pul...

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Autores principales: Ning, Li, Gao, Lei, Zhang, Fan, Li, Xiaoxiao, Wang, Tingting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626192/
https://www.ncbi.nlm.nih.gov/pubmed/34840974
http://dx.doi.org/10.1155/2021/5321121
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author Ning, Li
Gao, Lei
Zhang, Fan
Li, Xiaoxiao
Wang, Tingting
author_facet Ning, Li
Gao, Lei
Zhang, Fan
Li, Xiaoxiao
Wang, Tingting
author_sort Ning, Li
collection PubMed
description BACKGROUND: Intervertebral disc is responsible for absorbing and transmitting mechanical compression. Under physiological conditions, the peripheral annulus fibrosus (AF) cells are subjected to different magnitudes of transverse mechanical stretch depending on the swelling of the central nucleus pulposus tissue. However, the biological behavior of AF cells under mechanical stretch is not well studied. OBJECTIVE: This study was performed to study the effects of mechanical tension on AF cell senescence and the potential signaling transduction pathway. METHODS: Rat AF cells were made to experience different magnitudes of mechanical stretch (2% elongation and 20% elongation for 4 hours every day at 1 Hz) in a 10-day experiment period. The inhibitor RKI-1447 of the Rho-associated coiled-coil–containing protein kinases (ROCK) was added along with culture medium to investigate its role. Cell proliferation, cell cycle, telomerase activity, and expression of senescence markers (p16 and p53) were analyzed. RESULTS: We found that 20% elongation significantly decreased cell proliferation, promoted G0/G1 cell cycle arrest, decreased telomerase activity, and upregulated mRNA/protein expression of p16 and p53. Moreover, the inhibitor RKI-1447 partly resisted effects of 20% elongation on these parameters of cell senescence. CONCLUSION: High mechanical stretch obviously induces AF cell senescence through the RhoA/ROCK pathway. This study provides us a deeper understanding on the AF cell's behavior under mechanical stretch.
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spelling pubmed-86261922021-11-27 Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway Ning, Li Gao, Lei Zhang, Fan Li, Xiaoxiao Wang, Tingting Biomed Res Int Research Article BACKGROUND: Intervertebral disc is responsible for absorbing and transmitting mechanical compression. Under physiological conditions, the peripheral annulus fibrosus (AF) cells are subjected to different magnitudes of transverse mechanical stretch depending on the swelling of the central nucleus pulposus tissue. However, the biological behavior of AF cells under mechanical stretch is not well studied. OBJECTIVE: This study was performed to study the effects of mechanical tension on AF cell senescence and the potential signaling transduction pathway. METHODS: Rat AF cells were made to experience different magnitudes of mechanical stretch (2% elongation and 20% elongation for 4 hours every day at 1 Hz) in a 10-day experiment period. The inhibitor RKI-1447 of the Rho-associated coiled-coil–containing protein kinases (ROCK) was added along with culture medium to investigate its role. Cell proliferation, cell cycle, telomerase activity, and expression of senescence markers (p16 and p53) were analyzed. RESULTS: We found that 20% elongation significantly decreased cell proliferation, promoted G0/G1 cell cycle arrest, decreased telomerase activity, and upregulated mRNA/protein expression of p16 and p53. Moreover, the inhibitor RKI-1447 partly resisted effects of 20% elongation on these parameters of cell senescence. CONCLUSION: High mechanical stretch obviously induces AF cell senescence through the RhoA/ROCK pathway. This study provides us a deeper understanding on the AF cell's behavior under mechanical stretch. Hindawi 2021-11-19 /pmc/articles/PMC8626192/ /pubmed/34840974 http://dx.doi.org/10.1155/2021/5321121 Text en Copyright © 2021 Li Ning et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ning, Li
Gao, Lei
Zhang, Fan
Li, Xiaoxiao
Wang, Tingting
Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway
title Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway
title_full Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway
title_fullStr Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway
title_full_unstemmed Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway
title_short Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway
title_sort mechanical stretch induces annulus fibrosus cell senescence through activation of the rhoa/rock pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626192/
https://www.ncbi.nlm.nih.gov/pubmed/34840974
http://dx.doi.org/10.1155/2021/5321121
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