MiR‐223‐3p and miR‐22‐3p inhibit monosodium urate‐induced gouty inflammation by targeting NLRP3

Background MicroRNAs (miRNAs) have been shown to play a crucial role in inflammation regulation; however, their relationship with inflammation in acute gouty arthritis has not been fully elucidated. Herein, we conducted a study to explore the regulatory roles of miR‐223‐3p and miR‐22‐3p in gouty‐ass...

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Veröffentlicht in:International journal of rheumatic diseases 2021-04, Vol.24 (4), p.599-607
Hauptverfasser: Wang, Xiang, Chi, Jingwei, Dong, Bingzi, Xu, Lili, Zhou, Yue, Huang, Yajing, Sun, Shengnan, Wei, Fanxiang, Liu, Yuzhao, Liu, Chuanfeng, Che, Kui, Lv, Wenshan, Chen, Ying, Wang, Yangang
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Sprache:eng
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Zusammenfassung:Background MicroRNAs (miRNAs) have been shown to play a crucial role in inflammation regulation; however, their relationship with inflammation in acute gouty arthritis has not been fully elucidated. Herein, we conducted a study to explore the regulatory roles of miR‐223‐3p and miR‐22‐3p in gouty‐associated inflammation. Methods In vitro and in vivo experiments were conducted to examine the molecular mechanisms of miRNA regulation in gouty inflammation. Dual‐luciferase reporter assay was used to verify the direct target of miR‐223‐3p and miR‐22‐3p. Results We found that miR‐223‐3p and miR‐22‐3p interacted with the 3′ untranslated region segment of NLRP3 (nucleotide‐binding domain leucine‐rich repeat [NLR] and pyrin domain containing receptor 3) and inhibited its expression. A decreased expression of miR‐223‐3p and miR‐22‐3p was observed in both mice air pouch synovium and phorbol myristrate acetate‐treated THP‐1 cells stimulated with monosodium urate (P 
ISSN:1756-1841
1756-185X
DOI:10.1111/1756-185X.14089