Myricetin alleviated hydrogen peroxide-induced cellular senescence of nucleus pulposus cell through regulating SERPINE1

Abstract Background Myricetin (MYR) is a common plant flavonoid with antioxidant and anticancer properties. However, the anti-aging effect of MYR on nucleus pulposus cells (NPCs) is still unknown. The study aimed to explore the effect of MYR on the senescence of NPCs. Methods Methyl-thiazolyl tetraz...

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Published in:Journal of Orthopaedic Surgery and Research
Main Authors: Rongsheng Chen, Xiaobo Zhang, Xitian Zhu, Changsheng Wang, Weihong Xu
Format: Article
Language:English
Published: BMC 2023-02-01
Subjects:
Online Access:https://doi.org/10.1186/s13018-022-03463-0
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author Rongsheng Chen
Xiaobo Zhang
Xitian Zhu
Changsheng Wang
Weihong Xu
author_facet Rongsheng Chen
Xiaobo Zhang
Xitian Zhu
Changsheng Wang
Weihong Xu
author_sort Rongsheng Chen
collection DOAJ
container_title Journal of Orthopaedic Surgery and Research
description Abstract Background Myricetin (MYR) is a common plant flavonoid with antioxidant and anticancer properties. However, the anti-aging effect of MYR on nucleus pulposus cells (NPCs) is still unknown. The study aimed to explore the effect of MYR on the senescence of NPCs. Methods Methyl-thiazolyl tetrazolium assay was used to detect NPCs viability. Senescence level was evaluated by senescence-associated β-galactosidase (SA-β-Gal) staining and the expression levels of P21, P16, IL-6 and IL-8. RNA-Sequencing (RNA-seq) technology was used to identify differentially expressed genes (DEGs) between hydrogen peroxide + MYR (HO + MYR) group and HO group, and Gene Ontology (GO) functional was performed to analyze DEGs. A Venn diagram was generated to screen overlapping DEGs related to aging and inflammation, and the role of the promising validated DEG was selected for further investigation by gene functional assays. Results HO inhibited NPCs viability and stimulated the senescent phenotype of NPCs, whereas MYR treatment significantly reversed SA-β-gal activity in NPCs. MYR also reduced the expression of p21 and p16 and the secretion of IL-6 and IL-8 induced by HO. RNA-seq screened 421 DEGs. The GO enrichment results showed DEGs were mainly enriched in terms such as "sterol biosynthetic process". We also found SERPINE1 has the highest log2FC abs. Silence of SERPINE1 inhibited HO-induced NPCs senescence, and overexpression of SERPINE1 could limit the anti-aging effect of MYR. Conclusions MYR alleviated HO-induced senescence of NPCs by regulating SERPINE1 in vitro.
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spelling doaj-art-e8049d5a296c4071a03ea2f0d90311bc2025-08-19T19:17:37ZengBMCJournal of Orthopaedic Surgery and Research1749-799X2023-02-0118111110.1186/s13018-022-03463-0Myricetin alleviated hydrogen peroxide-induced cellular senescence of nucleus pulposus cell through regulating SERPINE1Rongsheng Chen0Xiaobo Zhang1Xitian Zhu2Changsheng Wang3Weihong Xu4Department of Spinal Surgery, The First Affiliated Hospital of Fujian Medical UniversityDepartment of Spinal Surgery, The First Affiliated Hospital of Fujian Medical UniversityDepartment of Spinal Surgery, The First Affiliated Hospital of Fujian Medical UniversityDepartment of Spinal Surgery, The First Affiliated Hospital of Fujian Medical UniversityDepartment of Spinal Surgery, The First Affiliated Hospital of Fujian Medical UniversityAbstract Background Myricetin (MYR) is a common plant flavonoid with antioxidant and anticancer properties. However, the anti-aging effect of MYR on nucleus pulposus cells (NPCs) is still unknown. The study aimed to explore the effect of MYR on the senescence of NPCs. Methods Methyl-thiazolyl tetrazolium assay was used to detect NPCs viability. Senescence level was evaluated by senescence-associated β-galactosidase (SA-β-Gal) staining and the expression levels of P21, P16, IL-6 and IL-8. RNA-Sequencing (RNA-seq) technology was used to identify differentially expressed genes (DEGs) between hydrogen peroxide + MYR (HO + MYR) group and HO group, and Gene Ontology (GO) functional was performed to analyze DEGs. A Venn diagram was generated to screen overlapping DEGs related to aging and inflammation, and the role of the promising validated DEG was selected for further investigation by gene functional assays. Results HO inhibited NPCs viability and stimulated the senescent phenotype of NPCs, whereas MYR treatment significantly reversed SA-β-gal activity in NPCs. MYR also reduced the expression of p21 and p16 and the secretion of IL-6 and IL-8 induced by HO. RNA-seq screened 421 DEGs. The GO enrichment results showed DEGs were mainly enriched in terms such as "sterol biosynthetic process". We also found SERPINE1 has the highest log2FC abs. Silence of SERPINE1 inhibited HO-induced NPCs senescence, and overexpression of SERPINE1 could limit the anti-aging effect of MYR. Conclusions MYR alleviated HO-induced senescence of NPCs by regulating SERPINE1 in vitro.https://doi.org/10.1186/s13018-022-03463-0MyricetinSenescenceNucleus pulposus cellsSERPINE1
spellingShingle Rongsheng Chen
Xiaobo Zhang
Xitian Zhu
Changsheng Wang
Weihong Xu
Myricetin alleviated hydrogen peroxide-induced cellular senescence of nucleus pulposus cell through regulating SERPINE1
Myricetin
Senescence
Nucleus pulposus cells
SERPINE1
title Myricetin alleviated hydrogen peroxide-induced cellular senescence of nucleus pulposus cell through regulating SERPINE1
title_full Myricetin alleviated hydrogen peroxide-induced cellular senescence of nucleus pulposus cell through regulating SERPINE1
title_fullStr Myricetin alleviated hydrogen peroxide-induced cellular senescence of nucleus pulposus cell through regulating SERPINE1
title_full_unstemmed Myricetin alleviated hydrogen peroxide-induced cellular senescence of nucleus pulposus cell through regulating SERPINE1
title_short Myricetin alleviated hydrogen peroxide-induced cellular senescence of nucleus pulposus cell through regulating SERPINE1
title_sort myricetin alleviated hydrogen peroxide induced cellular senescence of nucleus pulposus cell through regulating serpine1
topic Myricetin
Senescence
Nucleus pulposus cells
SERPINE1
url https://doi.org/10.1186/s13018-022-03463-0
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