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Circular RNA VMA21 ameliorates IL-1β-engendered chondrocyte injury through the miR-495-3p/FBWX7 signaling axis

This study explored the function of circular RNA VMA21 (circVMA21) in osteoarthritis (OA). IL-1β inducement reduced the expression of circVMA21 in C28/I2 cells and human primary chondrocytes. Forced expression of circVMA21 heightened cell viability and attenuated cell apoptosis, accompanied by upreg...

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Published in:Clinical immunology (Orlando, Fla.) Fla.), 2022-05, Vol.238, p.108995-108995, Article 108995
Main Authors: Li, ZhiFu, Meng, DongDong, Liu, YongYi, Bi, FangGang, Tian, Ke, Xu, JianZhong, Sun, JianGuang, Gu, ChenXi, Li, Yu
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cited_by cdi_FETCH-LOGICAL-c271t-c793242e94b173f89c113a44214beea11257c82933d9c35e71672b4881b99ea03
cites cdi_FETCH-LOGICAL-c271t-c793242e94b173f89c113a44214beea11257c82933d9c35e71672b4881b99ea03
container_end_page 108995
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container_start_page 108995
container_title Clinical immunology (Orlando, Fla.)
container_volume 238
creator Li, ZhiFu
Meng, DongDong
Liu, YongYi
Bi, FangGang
Tian, Ke
Xu, JianZhong
Sun, JianGuang
Gu, ChenXi
Li, Yu
description This study explored the function of circular RNA VMA21 (circVMA21) in osteoarthritis (OA). IL-1β inducement reduced the expression of circVMA21 in C28/I2 cells and human primary chondrocytes. Forced expression of circVMA21 heightened cell viability and attenuated cell apoptosis, accompanied by upregulation of Bcl-2, and downregulation of Bax and C-caspase-3 in C28/I2 cells in response to IL-1β exposure. CircVMA21 overexpression diminished the expression of MMP1 and MMP13, augmented the expression of COL2A1, and impeded the production of IL-6, TNF-α, prostaglandin E2 (PGE2) and NO. CircVMA21 served as a competitive endogenous RNA by sponging miR-495-3p. F-box and WD40 domain protein 7 (FBWX7) was identified as a target of miR-495-3p. The compensation experiments affirmed that circVMA21-mediated protective effects on IL-1β-irritated chondrocytes through the miR-495-3p/FBWX7 axis. The role of circVMA21 was also confirmed in an OA rat model. Collectively, these findings revealed a protective effect of circVMA21in OA by intercepting the miR-495-3p/FBWX7 crosstalk. •CircVMA21 was diminished in human chondrocytes challenged by IL-1β.•CircVMA21 protected chondrocytes against IL-1β-triggered apoptosis, inflammatory insult and cartilage degradation.•CircVMA21 functioned as a ceRNA by efficaciously sponging miR-495-3p thereby adjusting FBWX7 expression.•The miR-495-3p/FBWX7 axis participated in the protective roles of circVMA21 in IL-1β-engendered chondrocyte damage.
doi_str_mv 10.1016/j.clim.2022.108995
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IL-1β inducement reduced the expression of circVMA21 in C28/I2 cells and human primary chondrocytes. Forced expression of circVMA21 heightened cell viability and attenuated cell apoptosis, accompanied by upregulation of Bcl-2, and downregulation of Bax and C-caspase-3 in C28/I2 cells in response to IL-1β exposure. CircVMA21 overexpression diminished the expression of MMP1 and MMP13, augmented the expression of COL2A1, and impeded the production of IL-6, TNF-α, prostaglandin E2 (PGE2) and NO. CircVMA21 served as a competitive endogenous RNA by sponging miR-495-3p. F-box and WD40 domain protein 7 (FBWX7) was identified as a target of miR-495-3p. The compensation experiments affirmed that circVMA21-mediated protective effects on IL-1β-irritated chondrocytes through the miR-495-3p/FBWX7 axis. The role of circVMA21 was also confirmed in an OA rat model. Collectively, these findings revealed a protective effect of circVMA21in OA by intercepting the miR-495-3p/FBWX7 crosstalk. •CircVMA21 was diminished in human chondrocytes challenged by IL-1β.•CircVMA21 protected chondrocytes against IL-1β-triggered apoptosis, inflammatory insult and cartilage degradation.•CircVMA21 functioned as a ceRNA by efficaciously sponging miR-495-3p thereby adjusting FBWX7 expression.•The miR-495-3p/FBWX7 axis participated in the protective roles of circVMA21 in IL-1β-engendered chondrocyte damage.</description><identifier>ISSN: 1521-6616</identifier><identifier>EISSN: 1521-7035</identifier><identifier>DOI: 10.1016/j.clim.2022.108995</identifier><identifier>PMID: 35378300</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Apoptosis ; Apoptosis - genetics ; Chondrocytes - metabolism ; circVMA21 ; Extracellular matrix ; FBWX7 ; Interleukin-1beta - metabolism ; MicroRNAs - genetics ; MicroRNAs - metabolism ; miR-495-3p ; Osteoarthritis ; Osteoarthritis - genetics ; Osteoarthritis - metabolism ; Rats ; RNA, Circular - genetics ; Signal Transduction</subject><ispartof>Clinical immunology (Orlando, Fla.), 2022-05, Vol.238, p.108995-108995, Article 108995</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. 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Collectively, these findings revealed a protective effect of circVMA21in OA by intercepting the miR-495-3p/FBWX7 crosstalk. •CircVMA21 was diminished in human chondrocytes challenged by IL-1β.•CircVMA21 protected chondrocytes against IL-1β-triggered apoptosis, inflammatory insult and cartilage degradation.•CircVMA21 functioned as a ceRNA by efficaciously sponging miR-495-3p thereby adjusting FBWX7 expression.•The miR-495-3p/FBWX7 axis participated in the protective roles of circVMA21 in IL-1β-engendered chondrocyte damage.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - genetics</subject><subject>Chondrocytes - metabolism</subject><subject>circVMA21</subject><subject>Extracellular matrix</subject><subject>FBWX7</subject><subject>Interleukin-1beta - metabolism</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>miR-495-3p</subject><subject>Osteoarthritis</subject><subject>Osteoarthritis - genetics</subject><subject>Osteoarthritis - metabolism</subject><subject>Rats</subject><subject>RNA, Circular - genetics</subject><subject>Signal Transduction</subject><issn>1521-6616</issn><issn>1521-7035</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kMuOEzEQRS3EiHnAD7BAXrLpjKvcbbclNiFihpHCII147Sy3u5I46kewu0eT3-JD-CY6SmDJqkqlc69Uh7HXIGYgQF1vZ74J7QwF4nQojSmesQsoEDItZPH8tCsF6pxdprQVQhSI6gU7l4XUpRTigvWLEP3YuMgf7uf826c5AnctNaGPbqDE75YZ_P6VUbemrqZINfebvqtj7_cD8dBtx7jnwyb243ozTeJteMhyU2Ryd33z_vsPzVNYd64J3Zq7p5BesrOVaxK9Os0r9vXmw5fFx2z5-fZuMV9mHjUMmddGYo5k8gq0XJXGA0iX5wh5ReQAsNC-RCNlbbwsSIPSWOVlCZUx5IS8Ym-PvbvY_xwpDbYNyVPTuI76MVlUuUbAUqkJxSPqY59SpJXdxdC6uLcg7EG03dqDaHsQbY-ip9CbU_9YtVT_i_w1OwHvjgBNXz4Gijb5QJ2nOkTyg6378L_-PyykjMk</recordid><startdate>202205</startdate><enddate>202205</enddate><creator>Li, ZhiFu</creator><creator>Meng, DongDong</creator><creator>Liu, YongYi</creator><creator>Bi, FangGang</creator><creator>Tian, Ke</creator><creator>Xu, JianZhong</creator><creator>Sun, JianGuang</creator><creator>Gu, ChenXi</creator><creator>Li, Yu</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202205</creationdate><title>Circular RNA VMA21 ameliorates IL-1β-engendered chondrocyte injury through the miR-495-3p/FBWX7 signaling axis</title><author>Li, ZhiFu ; 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IL-1β inducement reduced the expression of circVMA21 in C28/I2 cells and human primary chondrocytes. Forced expression of circVMA21 heightened cell viability and attenuated cell apoptosis, accompanied by upregulation of Bcl-2, and downregulation of Bax and C-caspase-3 in C28/I2 cells in response to IL-1β exposure. CircVMA21 overexpression diminished the expression of MMP1 and MMP13, augmented the expression of COL2A1, and impeded the production of IL-6, TNF-α, prostaglandin E2 (PGE2) and NO. CircVMA21 served as a competitive endogenous RNA by sponging miR-495-3p. F-box and WD40 domain protein 7 (FBWX7) was identified as a target of miR-495-3p. The compensation experiments affirmed that circVMA21-mediated protective effects on IL-1β-irritated chondrocytes through the miR-495-3p/FBWX7 axis. The role of circVMA21 was also confirmed in an OA rat model. Collectively, these findings revealed a protective effect of circVMA21in OA by intercepting the miR-495-3p/FBWX7 crosstalk. •CircVMA21 was diminished in human chondrocytes challenged by IL-1β.•CircVMA21 protected chondrocytes against IL-1β-triggered apoptosis, inflammatory insult and cartilage degradation.•CircVMA21 functioned as a ceRNA by efficaciously sponging miR-495-3p thereby adjusting FBWX7 expression.•The miR-495-3p/FBWX7 axis participated in the protective roles of circVMA21 in IL-1β-engendered chondrocyte damage.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>35378300</pmid><doi>10.1016/j.clim.2022.108995</doi><tpages>1</tpages></addata></record>
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ispartof Clinical immunology (Orlando, Fla.), 2022-05, Vol.238, p.108995-108995, Article 108995
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subjects Animals
Apoptosis
Apoptosis - genetics
Chondrocytes - metabolism
circVMA21
Extracellular matrix
FBWX7
Interleukin-1beta - metabolism
MicroRNAs - genetics
MicroRNAs - metabolism
miR-495-3p
Osteoarthritis
Osteoarthritis - genetics
Osteoarthritis - metabolism
Rats
RNA, Circular - genetics
Signal Transduction
title Circular RNA VMA21 ameliorates IL-1β-engendered chondrocyte injury through the miR-495-3p/FBWX7 signaling axis
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