Met@MPDA rejuvenates BMSC energy metabolism to promote bone regeneration in semaglutide-treated obese periodontitis

  • Mater Today Bio. 2026 May 14:38:103231. doi: 10.1016/j.mtbio.2026.103231.
Ting Jiang  1  2  3  4  5  6  7 ,  Tian-Hao Wan  8  2  3  4  5  6  7 ,  Min-Jie Wang  1  2  3  4  5 ,  Xue-Qin Zhu  1  2  3  4  5 ,  Yu-Ran Jiang  1  2  3  4  5 ,  Feng Yang  1  2  3  4  5 ,  Zhi-Chen Ling  1  2  3  4  5 ,  Xin-Yi Tan  1  2  3  4  5 ,  Jun Wang  1  2  3  4  5  6  7 ,  Ning-Juan Ouyang  9  2  3  4  5  6  7
Affiliations
  • 1. Department of Pediatric Dentistry, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, China.
  • 2. College of Stomatology, Shanghai Jiao Tong University, China.
  • 3. National Center for Stomatology, National Clinical Research Center for Oral Diseases, China.
  • 4. Shanghai Key Laboratory of Stomatology, China.
  • 5. Shanghai Research Institute of Stomatology, Research Unit of Oral and Maxillofacial Regenerative Medicine, Chinese Academy of Medical Sciences, China.
  • 6. Oral Bioengineering Lab, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, China.
  • 7. National Clinical Research Center of Stomatology, Shanghai, China.
  • 8. Department of Oral Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, China.
  • 9. Department of Orthodontics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, China.
PMID: 42182879 DOI: 10.1016/j.mtbio.2026.103231
Abstract

Obesity is closely linked to periodontitis development. Although semaglutide is increasingly used to manage obesity, its effects on alveolar bone repair in periodontitis are not well understood. In a mouse model of obesity-related periodontitis, we found that obesity exacerbates alveolar bone loss in an inflammatory setting. Semaglutide treatment slightly reduced periodontal inflammation and osteoclast markers but did not improve osteogenesis or regenerate alveolar defects. Transcriptomic analysis revealed increased fatty-acid uptake but suppressed AMPK signaling and reduced fatty-acid oxidation (FAO) in inflamed alveolar bone of obese mice. In vitro, macrophage FAO was largely unaffected by inflammation or semaglutide, while FAO in bone marrow-derived mesenchymal stem cells (BMSCs) was significantly reduced, impairing osteogenic differentiation. To tackle metabolic and osteogenic issues, we created a metformin-loaded mesoporous polydopamine system (Met@MPDA) that acts as an AMPK agonist. Met@MPDA is absorbed by BMSCs, restoring cellular energy and promoting alveolar bone regeneration in periodontitis. While semaglutide provides anti-inflammatory benefits in obesity-related periodontitis, it falls short in boosting bone regeneration due to metabolic issues in BMSCs. Thus, Met@MPDA's sustained metformin delivery could enhance bone regeneration in these cases.

Keywords
AMPK; FAO; Obesity; Periodontitis; Semaglutide.
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