Cargando…
MicroRNA-195-5p inhibitor prevents the development of osteoarthritis by targeting REGγ
Osteoarthritis (OA) is a common inflammatory joint disease. MicroRNAs (miRNAs/miRs) have been reported to be involved in the pathogenesis of OA; however, the role of miRNAs in OA remains largely unexplained. The purpose of the present study was to investigate the expression and role of miR-195-5p in...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522802/ https://www.ncbi.nlm.nih.gov/pubmed/30942447 http://dx.doi.org/10.3892/mmr.2019.10124 |
_version_ | 1783419190196043776 |
---|---|
author | Shu, Yang Long, Junpeng Guo, Weixiong Ye, Wei |
author_facet | Shu, Yang Long, Junpeng Guo, Weixiong Ye, Wei |
author_sort | Shu, Yang |
collection | PubMed |
description | Osteoarthritis (OA) is a common inflammatory joint disease. MicroRNAs (miRNAs/miRs) have been reported to be involved in the pathogenesis of OA; however, the role of miRNAs in OA remains largely unexplained. The purpose of the present study was to investigate the expression and role of miR-195-5p in OA, and to further explore the mechanism. The expression level of miR-195-5p was measured using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). TargetScan and a luciferase reporter assay were used to reveal the associations between miR-195-5p and REGγ (also known as PSME3). To investigate the role of miR-195-5p in OA, a cell model of OA was established by treating ATDC5 cells with lipopolysaccharide (LPS). Then an MTT assay was conducted to detect cell proliferation ability, and an Annexin V-fluorescein isothiocyanate/propidium iodide apoptosis detection kit was used to measure cell apoptosis. In addition, the levels of interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α were determined using ELISA. Furthermore, gene and protein expression was measured via RT-qPCR and western blot assay, respectively. The results revealed that miR-195-5p was significantly upregulated in the articular cartilage tissues of patients with OA and in LPS stimulated ATDC5 cells. REGγ was a direct target of miR-195-5p. The repressed cell proliferation ability and enhanced cell apoptosis of ATDC5 cells induced by LPS were reversed by miR-195-5p downregulation. Furthermore, LPS stimulation significantly upregulated the levels of IL-1β, IL-6 and TNF-α, while miR-195-5p downregulation markedly reduced the expression of inflammatory factors induced by LPS. The results also revealed that a miR-195-5p inhibitor inhibited the LPS induced repression of the Wnt/β-catenin signaling pathway and activation of nuclear factor (NF)-κB signaling pathway in ATDC5 cells. Notably, the results of the present study also indicated that all of the effects of the miR-195-5p inhibitor on ATDC5 cells were reversed by REGγ silencing. In conclusion, the results indicated that the miR-195-5p inhibitor served a protective role in OA by inhibiting chondrocyte apoptosis and inflammatory responses by regulating the Wnt/β-catenin and NF-κB signaling pathways. |
format | Online Article Text |
id | pubmed-6522802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-65228022019-06-18 MicroRNA-195-5p inhibitor prevents the development of osteoarthritis by targeting REGγ Shu, Yang Long, Junpeng Guo, Weixiong Ye, Wei Mol Med Rep Articles Osteoarthritis (OA) is a common inflammatory joint disease. MicroRNAs (miRNAs/miRs) have been reported to be involved in the pathogenesis of OA; however, the role of miRNAs in OA remains largely unexplained. The purpose of the present study was to investigate the expression and role of miR-195-5p in OA, and to further explore the mechanism. The expression level of miR-195-5p was measured using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). TargetScan and a luciferase reporter assay were used to reveal the associations between miR-195-5p and REGγ (also known as PSME3). To investigate the role of miR-195-5p in OA, a cell model of OA was established by treating ATDC5 cells with lipopolysaccharide (LPS). Then an MTT assay was conducted to detect cell proliferation ability, and an Annexin V-fluorescein isothiocyanate/propidium iodide apoptosis detection kit was used to measure cell apoptosis. In addition, the levels of interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α were determined using ELISA. Furthermore, gene and protein expression was measured via RT-qPCR and western blot assay, respectively. The results revealed that miR-195-5p was significantly upregulated in the articular cartilage tissues of patients with OA and in LPS stimulated ATDC5 cells. REGγ was a direct target of miR-195-5p. The repressed cell proliferation ability and enhanced cell apoptosis of ATDC5 cells induced by LPS were reversed by miR-195-5p downregulation. Furthermore, LPS stimulation significantly upregulated the levels of IL-1β, IL-6 and TNF-α, while miR-195-5p downregulation markedly reduced the expression of inflammatory factors induced by LPS. The results also revealed that a miR-195-5p inhibitor inhibited the LPS induced repression of the Wnt/β-catenin signaling pathway and activation of nuclear factor (NF)-κB signaling pathway in ATDC5 cells. Notably, the results of the present study also indicated that all of the effects of the miR-195-5p inhibitor on ATDC5 cells were reversed by REGγ silencing. In conclusion, the results indicated that the miR-195-5p inhibitor served a protective role in OA by inhibiting chondrocyte apoptosis and inflammatory responses by regulating the Wnt/β-catenin and NF-κB signaling pathways. D.A. Spandidos 2019-06 2019-04-03 /pmc/articles/PMC6522802/ /pubmed/30942447 http://dx.doi.org/10.3892/mmr.2019.10124 Text en Copyright: © Shu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Shu, Yang Long, Junpeng Guo, Weixiong Ye, Wei MicroRNA-195-5p inhibitor prevents the development of osteoarthritis by targeting REGγ |
title | MicroRNA-195-5p inhibitor prevents the development of osteoarthritis by targeting REGγ |
title_full | MicroRNA-195-5p inhibitor prevents the development of osteoarthritis by targeting REGγ |
title_fullStr | MicroRNA-195-5p inhibitor prevents the development of osteoarthritis by targeting REGγ |
title_full_unstemmed | MicroRNA-195-5p inhibitor prevents the development of osteoarthritis by targeting REGγ |
title_short | MicroRNA-195-5p inhibitor prevents the development of osteoarthritis by targeting REGγ |
title_sort | microrna-195-5p inhibitor prevents the development of osteoarthritis by targeting regγ |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522802/ https://www.ncbi.nlm.nih.gov/pubmed/30942447 http://dx.doi.org/10.3892/mmr.2019.10124 |
work_keys_str_mv | AT shuyang microrna1955pinhibitorpreventsthedevelopmentofosteoarthritisbytargetingregg AT longjunpeng microrna1955pinhibitorpreventsthedevelopmentofosteoarthritisbytargetingregg AT guoweixiong microrna1955pinhibitorpreventsthedevelopmentofosteoarthritisbytargetingregg AT yewei microrna1955pinhibitorpreventsthedevelopmentofosteoarthritisbytargetingregg |