Transglutaminase 2 inhibitors attenuate osteoarthritic degeneration of TMJ-osteoarthritis by suppressing NF-κB activation

Background: The temporomandibular joint osteoarthritis (TMJ-OA) is characterized by progressive cartilage degradation, subchondral bone erosion, and chronic pain, leading to articular damage and chewing dysfunction. Studies have shown that interleukin-1 beta (IL-1 beta) plays a critical role in the development of TMJ-OA. Transglutaminase 2 (TG2) has been identified as a marker of chondrocyte hypertrophy and IL-1 beta was able to increase TG2 expression in chondrocytes. Therefore, the aim of this study was to explore the ability of TG2 inhibitors to suppress TMJ-OA progression. Methods: Firstly, toluidine blue staining, cell counting kit-8 assay, immunocytofluorescent staining and western blot were used to investigate the anti-inflammatory effects of TG2 inhibitors in IL-1 beta-stimulated murine chondrocytes and the underlying mechanisms. Afterwards, micro-CT analysis, histological staining, immunohistochemical and immunohistofluorescent staining were used to evaluate the therapeutic efficacy of TG2 inhibitors in monosodium iodoacetate (MIA)-induced TMJ-OA in rats. Results: TG2 inhibitors suppressed the IL-1 beta-induced upregulation of COX-2, iNOS, MMP-13, and MMP-3 and reversed the IL-1 beta-induced proteoglycan loss in chondrocytes through inhibiting NF-kappa B activation. Consistently, the MIA-induced upregulation of MMP-13 and MMP-3, and loss of structural integrity of the articular cartilage and subchondral bone were markedly reversed by TG2 inhibitors via inhibiting NF-kappa B activation. Conclusions: TG2 inhibitors demonstrated a potent therapeutic efficacy on cartilage and subchondral bone structures of TMJ-OA by reducing inflammation and cartilage degradation through suppressing NF-kappa B activation.

Automated summary

This study aimed to explore the ability of TG2 inhibitors to suppress TMJ-OA progression. The results showed that TG2 inhibitors suppressed inflammation and cartilage degradation by inhibiting NF-kappa B activation, leading to significant reversal of structural damage in TMJ-OA. These findings suggest the potential therapeutic efficacy of TG2 inhibitors in the treatment of TMJ-OA.