SOX11 Alleviates Osteoarthritis through Reducing Mitochondrial Dysfunction and Ferroptosis via Binding to the Promoter of NOX4

Xingchang Fu, Gang Yang^*
Department of Joint Surgery, Hunan Aerospace Hospital, Changsha, China
* Corresponding Author: Gang Yang. Email: email
(This article belongs to the Special Issue: Modulation of Inflammation, Oxidative Stress, and Mitochondrial Function: Therapeutic Perspectives Across Diseases)

BIOCELL https://doi.org/10.32604/biocell.2026.074951

Received 22 October 2025; Accepted 15 January 2026; Published online 18 February 2026

Abstract

Objectives: Mitochondrial dysfunction and ferroptosis play crucial roles in osteoarthritis (OA), but the mechanisms remain unclear. This study aims to investigate the mechanism of sex-determining region Y-box transcription factor (SOX) 11/nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 4 (NOX4) axis-mediated mitochondrial dysfunction and ferroptosis in OA. Methods: Destabilization of the medial meniscus (DMM) induced knee OA in mice. Chondrocytes were stimulated with IL-1β. Ferroptosis and mitochondrial function-related indicators were detected by immunofluorescence, 5,5^′,6,6^′-Tetrachloro-1,1^′,3,3^′-tetraethyl-imidacarbocyanine iodide (JC-1) staining, flow cytometry, quantitative real-time polymerase chain reaction (qRT-PCR), and Western blot. Results: OA mice had 4.4 and 1.1-fold increase in SOX11 and NOX4 proteins (p < 0.05). ChIP-qPCR and dual-luciferase reporter gene assays confirmed that SOX11 directly bound to the NOX4 promoter. Knocking SOX11 inhibited NOX4 and acyl-CoA synthetase long-chain family member 4 (ACSL4) levels in IL-1β-induced chondrocytes, promoted glutathione peroxidase 4 (GPX4) and solute carrier family 7 member 11 (SLC7A11) expression, and reduced Fe²⁺ concentration and cell death. Additionally, SOX11 knockdown inhibited lipid peroxidation and ROS production and malondialdehyde (MDA) level, increased mitochondrial membrane potential, GSH, and SOD levels. NOX4 overexpression interrupted the beneficial effects. In vivo experiments further validated that SOX11 knockdown reduced cartilage damage and Osteoarthritis Research Society International (OARSI) score, increased the transparent cartilage layer thickness, reduced calcified cartilage thickness, inhibited ferroptosis, and mitochondrial dysfunction. Conclusion: Our results indicate that SOX11 inhibition reduces mitochondrial dysfunction and ferroptosis in IL-1β-induced chondrocytes by downregulating NOX4, thereby alleviating OA. This finding provides new targets for OA treatment.