KDM6B promotes ferroptosis in rheumatoid arthritis fibroblast-like synoviocytes via the miR-128-3p/SLC7A11 axis through H3K27me3 modification

J Orthop Surg Res. 2025 Sep 29;20(1):862. doi: 10.1186/s13018-025-06277-y.

Abstract

Background: Rheumatoid arthritis (RA) is a chronic inflammatory joint disease, primarily driven by fibroblast-like synoviocytes (FLSs) that trigger synovial inflammation and joint destruction. This study explores the mechanisms of KDM6B in ferroptosis in RA-FLSs, providing a theoretical basis for the treatment of RA.

Methods: RA-FLSs were isolated from RA synovial tissue samples. si-KDM6B was transfected into RA-FLSs, followed by the detection of KDM6B and miR-128-3p using qRT-PCR and Western blot. Cell viability was assessed using the CCK-8 assay. The levels of ROS, GSH, MDA, and Fe2+ were evaluated, and the expression of GPX4, SLC7A11, and ACSL4 was measured. The enrichment of KDM6B and H3K27me3 on the miR-128-3p promoter was detected by ChIP. The binding relationship between miR-128-3p and SLC7A11 was validated by dual-luciferase reporter assay. Combined experiments were designed to validate the mechanism.

Results: KDM6B was highly expressed in RA tissues and RA-FLSs. Inhibition of KDM6B increased cell viability, elevated ROS, MDA, and Fe2+, decreased GSH, reduced GPX4 and SLC7A11, and increased ACSL4. KDM6B and H3K27me3 were enriched on the miR-128-3p promoter. Inhibition of KDM6B increased H3K27me3 enrichment and suppressed miR-128-3p expression. miR-128-3p targeted and inhibited SLC7A11 expression. miR-128-3p overexpression or SLC7A11 inhibition partially reversed the inhibitory effect of KDM6B inhibition on ferroptosis in RA-FLSs.

Conclusion: KDM6B promotes ferroptosis in RA-FLSs via the miR-128-3p/SLC7A11 axis through the removal of histone H3K27me3 modification.

Keywords: Ferroptosis; Fibroblast-like synoviocytes; KDM6B; Rheumatoid arthritis; miR-128-3p.

MeSH terms

  • Amino Acid Transport System y+* / genetics
  • Amino Acid Transport System y+* / metabolism
  • Arthritis, Rheumatoid* / genetics
  • Arthritis, Rheumatoid* / metabolism
  • Arthritis, Rheumatoid* / pathology
  • Cell Survival / genetics
  • Cells, Cultured
  • Ferroptosis* / genetics
  • Ferroptosis* / physiology
  • Fibroblasts* / metabolism
  • Fibroblasts* / pathology
  • Histones* / metabolism
  • Humans
  • Jumonji Domain-Containing Histone Demethylases* / genetics
  • Jumonji Domain-Containing Histone Demethylases* / metabolism
  • Jumonji Domain-Containing Histone Demethylases* / physiology
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Synoviocytes* / metabolism
  • Synoviocytes* / pathology

Substances

  • MicroRNAs
  • Jumonji Domain-Containing Histone Demethylases
  • KDM6B protein, human
  • Amino Acid Transport System y+
  • SLC7A11 protein, human
  • MIRN128 microRNA, human
  • Histones