2. Academic Validation
  3. OGT regulates histone demethylation and alleviates osteoarthritis progression by O-GlcNAcylation of KDM6B

OGT regulates histone demethylation and alleviates osteoarthritis progression by O-GlcNAcylation of KDM6B

  • J Adv Res. 2026 Jan 2:S2090-1232(26)00003-2. doi: 10.1016/j.jare.2026.01.003.
Xiang Gao 1,  Hang Liu 2,  Jianming Guo 3,  Gengze Li 4,  Xinyu Yang 5,  Xinliang Peng 6,  Yifan Ren 7,  Xianding Sun 8,  Chao Liang 9,  Yu Du 10
Affiliations

Affiliations

  • 1 Department of Orthopedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China. Electronic address: [email protected].
  • 2 Department of Orthopedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China. Electronic address: [email protected].
  • 3 Department of Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China; Institute of Integrated Bioinfomedicine and Translational Science (IBTS), School of Chinese Medicine, Hong Kong Baptist University, 999077, Hong Kong, China. Electronic address: [email protected].
  • 4 Department of Orthopedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China. Electronic address: [email protected].
  • 5 Department of Orthopedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China. Electronic address: [email protected].
  • 6 Department of Orthopedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China. Electronic address: [email protected].
  • 7 Department of Orthopedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China. Electronic address: [email protected].
  • 8 Department of Orthopedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China. Electronic address: [email protected].
  • 9 Department of Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China; Institute of Integrated Bioinfomedicine and Translational Science (IBTS), School of Chinese Medicine, Hong Kong Baptist University, 999077, Hong Kong, China; State Key Laboratory of Proteomics, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, Beijing 100850, China. Electronic address: [email protected].
  • 10 Department of Orthopedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing 400010, China. Electronic address: [email protected].
PMID: 41485575 DOI: 10.1016/j.jare.2026.01.003
Abstract

Objective: Osteoarthritis (OA) is a common orthopedic disease characterized by cartilage degeneration, osteophyte formation, and synovial hyperplasia. Although dysregulated O-GlcNAcylation has been implicated in various musculoskeletal and inflammatory disorders, its specific role and molecular targets in OA pathogenesis remain largely unexplored. In this study, we aimed to conduct a multidimensional investigation to demonstrate and delineate the chondrocyte-specific functions and mechanisms of O-GlcNAc transferase (OGT) during OA progression.

Methods: To explore the mechanisms of OA progression, we analyzed OGT expression using GEO data and clinical cartilage samples. Cartilage-specific OGT knockout mice (Acan-CreERT2; OGTflox/flox) were generated and subjected to DMM surgery. To determine the effects of OGT in OA, histological and immunohistochemical studies were conducted. RNA-seq and CUT&Tag were were employed to elucidate the underlying molecular mechanisms.

Results: OGT expression is reduced in OA cartilage, and its overexpression delays cartilage degeneration, while cartilage-specific OGT deletion accelerates OA progression. Mechanistically, we found that OGT interacts with and O-GlcNAcylates KDM6B at serine 215, thereby inhibiting its ubiquitination, enhancing protein stability, and promoting extracellular matrix gene expression by demethylating H3K27me3 at Col2a1 and Col6a6 loci.

Conclusions: OGT is a key regulator of OA that exerts its function by modulating the epigenetic state of chondrocytes. Loss of OGT in chondrocytes not only disrupts normal cartilage development but also accelerates OA progression under pathological conditions, thereby providing new experimental evidence for understanding OA pathogenesis and informing the development of potential therapeutic strategies.

Keywords

Demethylation; Epigenetic modification; KDM6B; OGT; Osteoarthritis.

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