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Background <p>Regulatory T (Treg) cells are essential for maintaining immune tolerance and have been implicated in tissue regeneration; however, their role in periodontal regeneration remains poorly understood. This study aimed to elucidate the effect of Treg cell-derived exosomes (Treg-Exos), particularly those carrying microRNA-21 (miR-21), on the osteogenic differentiation of periodontal ligament stem cells (PDLSCs) and periodontal tissue regeneration.</p> Methods <p>After co-culturing Treg cells or Treg-Exos with PDLSCs respectively in vitro, the osteogenic differentiation of treated PDLSCs was assessed through Alkaline phosphatase (ALP) activity, Alizarin Red staining, and the expression of osteogenic markers runt-related transcription factor 2 (Runx-2) and Osterix. The functional role of miR-21 in Treg-Exos was assessed via gain- and loss-of-function experiments, involving transfection of Treg cells with miR-21 mimics or inhibitors. In vivo, a mice periodontal defect model was established via silk ligation and Porphyromonas gingivalis inoculation. Subsequently, Treg-Exos were locally administered into defects to assess their potential in promoting periodontal tissue regeneration. The regenerative efficacy was evaluated using micro-CT and histological analysis.</p> Results <p>Treg cell levels were significantly elevated in periodontitis patients compared to healthy controls. Both Treg cells and Treg-Exos markedly promoted the osteogenic differentiation of PDLSCs in vitro, as evidenced by increased ALP activity, enhanced mineralization, and upregulated Runx-2/Osterix expression. Exosomes derived from miR-21-overexpressing Treg cells further promoted PDLSC osteogenesis, whereas exosomes with miR-21 knockdown exhibited an inhibitory effect. In vivo, Treg-Exos injection alleviated periodontal damage and improved tissue morphology compared to PBS controls, as demonstrated by micro-CT and histological analyses.</p> Conclusion <p>Treg cell-derived exosomal miR-21 promotes the osteogenic differentiation of PDLSCs, enhancing periodontal tissue regeneration in vivo, suggesting that Treg cells and their exosomal miR-21 may serve as promising therapeutic targets for periodontitis.</p>

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Treg cell-derived exosomal miR-21 promotes osteogenic differentiation of periodontal ligament stem cells

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年9月26日

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  • Yu Xia,
  • Hao Jiang,
  • Chen Wang,
  • Zhen Liu,
  • Hui Gao,
  • Ji-Feng Yu,
  • Nan Yang,
  • Li Liang

摘要

Background

Regulatory T (Treg) cells are essential for maintaining immune tolerance and have been implicated in tissue regeneration; however, their role in periodontal regeneration remains poorly understood. This study aimed to elucidate the effect of Treg cell-derived exosomes (Treg-Exos), particularly those carrying microRNA-21 (miR-21), on the osteogenic differentiation of periodontal ligament stem cells (PDLSCs) and periodontal tissue regeneration.

Methods

After co-culturing Treg cells or Treg-Exos with PDLSCs respectively in vitro, the osteogenic differentiation of treated PDLSCs was assessed through Alkaline phosphatase (ALP) activity, Alizarin Red staining, and the expression of osteogenic markers runt-related transcription factor 2 (Runx-2) and Osterix. The functional role of miR-21 in Treg-Exos was assessed via gain- and loss-of-function experiments, involving transfection of Treg cells with miR-21 mimics or inhibitors. In vivo, a mice periodontal defect model was established via silk ligation and Porphyromonas gingivalis inoculation. Subsequently, Treg-Exos were locally administered into defects to assess their potential in promoting periodontal tissue regeneration. The regenerative efficacy was evaluated using micro-CT and histological analysis.

Results

Treg cell levels were significantly elevated in periodontitis patients compared to healthy controls. Both Treg cells and Treg-Exos markedly promoted the osteogenic differentiation of PDLSCs in vitro, as evidenced by increased ALP activity, enhanced mineralization, and upregulated Runx-2/Osterix expression. Exosomes derived from miR-21-overexpressing Treg cells further promoted PDLSC osteogenesis, whereas exosomes with miR-21 knockdown exhibited an inhibitory effect. In vivo, Treg-Exos injection alleviated periodontal damage and improved tissue morphology compared to PBS controls, as demonstrated by micro-CT and histological analyses.

Conclusion

Treg cell-derived exosomal miR-21 promotes the osteogenic differentiation of PDLSCs, enhancing periodontal tissue regeneration in vivo, suggesting that Treg cells and their exosomal miR-21 may serve as promising therapeutic targets for periodontitis.