miR-520c-3p regulates IL-1β-stimulated human chondrocyte apoptosis and cartilage degradation by targeting GAS2

Abstract Background MicroRNAs (miRNAs) have been shown to be associated with osteoarthritis (OA) progression. This study aimed to explore the role of miR-520c-3p in OA progression. Methods Expression levels of miR-520c-3p and Growth arrest-specific 2 (GAS2) were detected using quantitative real-time...

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Main Authors: Le Peng, Ming Deng, Yonggang Ma, Wei Hu, Fan Liang
Format: Article
Language:English
Published: BMC 2021-05-01
Series:Journal of Orthopaedic Surgery and Research
Subjects:
Online Access:https://doi.org/10.1186/s13018-021-02466-7
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author Le Peng
Ming Deng
Yonggang Ma
Wei Hu
Fan Liang
author_facet Le Peng
Ming Deng
Yonggang Ma
Wei Hu
Fan Liang
author_sort Le Peng
collection DOAJ
description Abstract Background MicroRNAs (miRNAs) have been shown to be associated with osteoarthritis (OA) progression. This study aimed to explore the role of miR-520c-3p in OA progression. Methods Expression levels of miR-520c-3p and Growth arrest-specific 2 (GAS2) were detected using quantitative real-time PCR. The proliferation and apoptosis of cells were measured using cell counting kit 8 (CCK8) assay and flow cytometry. Furthermore, the protein levels of apoptosis-related markers, extracellular degradation markers, inflammatory response markers, and GAS2 were tested using quantitative real-time polymerase chain reaction (RT-PCR) and western blot (WB) analysis. In addition, the interaction between miR-520c-3p and GAS2 was examined using dual luciferase reporter assay. Results GAS2 was highly expressed, and miR-520c-3p was lowly expressed in OA cartilage tissues. miR-520c-3p could promote the proliferation and inhibit the apoptosis and inflammation of OA chondrocytes. miR-520c-3p could be sponged by GAS2, and its inhibitor could reverse the regulation of GAS2 on the biological functions of OA chondrocytes. GAS2 was a target of miR-520c-3p, which was identified by bioinformatic analysis and dual-luciferase reporter assay. Overexpression of GAS2 could inhibit the proliferation and promoted the apoptosis and inflammation of OA chondrocytes. Conclusion Our data showed that miR-520c-3p might regulate the GAS2 to inhibit the progression of OA.
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spelling doaj.art-44ebb156af5a4c4ca027707f94666ebb2022-12-22T02:54:25ZengBMCJournal of Orthopaedic Surgery and Research1749-799X2021-05-011611910.1186/s13018-021-02466-7miR-520c-3p regulates IL-1β-stimulated human chondrocyte apoptosis and cartilage degradation by targeting GAS2Le Peng0Ming Deng1Yonggang Ma2Wei Hu3Fan Liang4Department of Orthopaedics, Renmin Hospital of Wuhan UniversityDepartment of Orthopaedics, Renmin Hospital of Wuhan UniversityDepartment of Orthopaedics, Renmin Hospital of Wuhan UniversityDepartment of Orthopaedics, Renmin Hospital of Wuhan UniversityDepartment of Orthopaedics, Renmin Hospital of Wuhan UniversityAbstract Background MicroRNAs (miRNAs) have been shown to be associated with osteoarthritis (OA) progression. This study aimed to explore the role of miR-520c-3p in OA progression. Methods Expression levels of miR-520c-3p and Growth arrest-specific 2 (GAS2) were detected using quantitative real-time PCR. The proliferation and apoptosis of cells were measured using cell counting kit 8 (CCK8) assay and flow cytometry. Furthermore, the protein levels of apoptosis-related markers, extracellular degradation markers, inflammatory response markers, and GAS2 were tested using quantitative real-time polymerase chain reaction (RT-PCR) and western blot (WB) analysis. In addition, the interaction between miR-520c-3p and GAS2 was examined using dual luciferase reporter assay. Results GAS2 was highly expressed, and miR-520c-3p was lowly expressed in OA cartilage tissues. miR-520c-3p could promote the proliferation and inhibit the apoptosis and inflammation of OA chondrocytes. miR-520c-3p could be sponged by GAS2, and its inhibitor could reverse the regulation of GAS2 on the biological functions of OA chondrocytes. GAS2 was a target of miR-520c-3p, which was identified by bioinformatic analysis and dual-luciferase reporter assay. Overexpression of GAS2 could inhibit the proliferation and promoted the apoptosis and inflammation of OA chondrocytes. Conclusion Our data showed that miR-520c-3p might regulate the GAS2 to inhibit the progression of OA.https://doi.org/10.1186/s13018-021-02466-7miR-520c-3pGAS2OsteoarthritisApoptosis
spellingShingle Le Peng
Ming Deng
Yonggang Ma
Wei Hu
Fan Liang
miR-520c-3p regulates IL-1β-stimulated human chondrocyte apoptosis and cartilage degradation by targeting GAS2
Journal of Orthopaedic Surgery and Research
miR-520c-3p
GAS2
Osteoarthritis
Apoptosis
title miR-520c-3p regulates IL-1β-stimulated human chondrocyte apoptosis and cartilage degradation by targeting GAS2
title_full miR-520c-3p regulates IL-1β-stimulated human chondrocyte apoptosis and cartilage degradation by targeting GAS2
title_fullStr miR-520c-3p regulates IL-1β-stimulated human chondrocyte apoptosis and cartilage degradation by targeting GAS2
title_full_unstemmed miR-520c-3p regulates IL-1β-stimulated human chondrocyte apoptosis and cartilage degradation by targeting GAS2
title_short miR-520c-3p regulates IL-1β-stimulated human chondrocyte apoptosis and cartilage degradation by targeting GAS2
title_sort mir 520c 3p regulates il 1β stimulated human chondrocyte apoptosis and cartilage degradation by targeting gas2
topic miR-520c-3p
GAS2
Osteoarthritis
Apoptosis
url https://doi.org/10.1186/s13018-021-02466-7
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AT mingdeng mir520c3pregulatesil1bstimulatedhumanchondrocyteapoptosisandcartilagedegradationbytargetinggas2
AT yonggangma mir520c3pregulatesil1bstimulatedhumanchondrocyteapoptosisandcartilagedegradationbytargetinggas2
AT weihu mir520c3pregulatesil1bstimulatedhumanchondrocyteapoptosisandcartilagedegradationbytargetinggas2
AT fanliang mir520c3pregulatesil1bstimulatedhumanchondrocyteapoptosisandcartilagedegradationbytargetinggas2