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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 |
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container_title | Clinical immunology (Orlando, Fla.) |
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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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•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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c271t-c793242e94b173f89c113a44214beea11257c82933d9c35e71672b4881b99ea03</citedby><cites>FETCH-LOGICAL-c271t-c793242e94b173f89c113a44214beea11257c82933d9c35e71672b4881b99ea03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35378300$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, ZhiFu</creatorcontrib><creatorcontrib>Meng, DongDong</creatorcontrib><creatorcontrib>Liu, YongYi</creatorcontrib><creatorcontrib>Bi, FangGang</creatorcontrib><creatorcontrib>Tian, Ke</creatorcontrib><creatorcontrib>Xu, JianZhong</creatorcontrib><creatorcontrib>Sun, JianGuang</creatorcontrib><creatorcontrib>Gu, ChenXi</creatorcontrib><creatorcontrib>Li, Yu</creatorcontrib><title>Circular RNA VMA21 ameliorates IL-1β-engendered chondrocyte injury through the miR-495-3p/FBWX7 signaling axis</title><title>Clinical immunology (Orlando, Fla.)</title><addtitle>Clin Immunol</addtitle><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.</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 ; Meng, DongDong ; Liu, YongYi ; Bi, FangGang ; Tian, Ke ; Xu, JianZhong ; Sun, JianGuang ; Gu, ChenXi ; Li, Yu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c271t-c793242e94b173f89c113a44214beea11257c82933d9c35e71672b4881b99ea03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - genetics</topic><topic>Chondrocytes - metabolism</topic><topic>circVMA21</topic><topic>Extracellular matrix</topic><topic>FBWX7</topic><topic>Interleukin-1beta - metabolism</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>miR-495-3p</topic><topic>Osteoarthritis</topic><topic>Osteoarthritis - genetics</topic><topic>Osteoarthritis - metabolism</topic><topic>Rats</topic><topic>RNA, Circular - genetics</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, ZhiFu</creatorcontrib><creatorcontrib>Meng, DongDong</creatorcontrib><creatorcontrib>Liu, YongYi</creatorcontrib><creatorcontrib>Bi, FangGang</creatorcontrib><creatorcontrib>Tian, Ke</creatorcontrib><creatorcontrib>Xu, JianZhong</creatorcontrib><creatorcontrib>Sun, JianGuang</creatorcontrib><creatorcontrib>Gu, ChenXi</creatorcontrib><creatorcontrib>Li, Yu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical immunology (Orlando, Fla.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, ZhiFu</au><au>Meng, DongDong</au><au>Liu, YongYi</au><au>Bi, FangGang</au><au>Tian, Ke</au><au>Xu, JianZhong</au><au>Sun, JianGuang</au><au>Gu, ChenXi</au><au>Li, Yu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Circular RNA VMA21 ameliorates IL-1β-engendered chondrocyte injury through the miR-495-3p/FBWX7 signaling axis</atitle><jtitle>Clinical immunology (Orlando, Fla.)</jtitle><addtitle>Clin Immunol</addtitle><date>2022-05</date><risdate>2022</risdate><volume>238</volume><spage>108995</spage><epage>108995</epage><pages>108995-108995</pages><artnum>108995</artnum><issn>1521-6616</issn><eissn>1521-7035</eissn><abstract>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.</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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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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