Chinese Herbal Formula Huayu-Qiangshen-Tongbi Decoction Attenuates Rheumatoid Arthritis through Upregulating miR-125b to Suppress NF- κ B-Induced Inflammation by Targeting CK2

J Immunol Res. 2022 Jul 4:2022:2836128. doi: 10.1155/2022/2836128. eCollection 2022.

Abstract

The Huayu-Qiangshen-Tongbi (HQT) decoction, a Chinese medical formula, has been identified to show a potent therapeutic effect on rheumatoid arthritis (RA). However, the specific molecular mechanism of HQT in RA has not been well studied. In the present study, LPS-treated human rheumatoid fibroblast-like synoviocyte (FLS) MH7A cells and collagen-induced arthritis (CIA) mice were utilized as in vitro and in vivo models. Our results demonstrated that HQT could efficiently inhibit RA-induced inflammation by reducing the production of cytokines including tumor necrosis factor alpha (TNF-α), interleukin-1 beta (IL-1β), and interleukin-6 (IL-6). Moreover, HQT significantly upregulated the expression of miR-125b. Besides, analysis of bioinformatics suggested casein kinase 2 (CK2) was a potential target of miR-125b. Luciferase reporter assay was performed and revealed that miR-125b suppressed CK2 expression in MH7A cells. Furthermore, miR-125b inhibited LPS-induced NF-kappa-B (NF-κB) activation, which is a downstream target of CK2. In addition, the NF-κB inhibitor ammonium pyrrolidinedithiocarbamate (PDTC) and NF-kappa-B inhibitor alpha (IkB-α) enhanced the inhibitory effect of miR-125b on the expression of TNF-α, IL-1β, and IL-6. Taken together, our study revealed that HQT could attenuate RA through upregulating miR-125b to suppress NF-κB-induced inflammation by targeting CK2. The findings of this study should facilitate investigating the mechanism of HQT on RA and discovering novel therapeutic targets for RA.

MeSH terms

  • Animals
  • Arthritis, Rheumatoid* / metabolism
  • Casein Kinase II / genetics
  • Casein Kinase II / metabolism
  • Casein Kinase II / pharmacology
  • China
  • Fibroblasts
  • Humans
  • Inflammation / metabolism
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / pharmacology
  • Mice
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • NF-kappa B / metabolism
  • Synoviocytes* / pathology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-6
  • Lipopolysaccharides
  • MicroRNAs
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • Casein Kinase II