Zhao Weiwei, Ji Lingli, Li Jie, Liu Dandan, Zhang Chenying, Wang Xiaozhe, Liu Yang, Zheng Shuguo
Department of Preventive Dentistry, Peking University School and Hospital of Stomatology & National Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology & NHC Key Laboratory of Digital Stomatology & NMPA Key Laboratory for Dental Materials, Beijing, 100081, PR China.
Inflammation. 2025 Aug 8. doi: 10.1007/s10753-025-02348-8.
This study aims to explore the mechanism by which heat-inactivated Bacillus subtilis (B. subtilis) R0179 modulates the TLR2/NF-κB signaling pathway to inhibit Porphyromonas gingivalis (P. gingivalis) induced gingival inflammation. In vitro experiments showed that P. gingivalis could invade gingival epithelial cells within 2 h of infection, as observed by transmission electron microscopy, and infection with P. gingivalis upregulated the expression of TLR1, TLR2, TLR4, TLR6, and p-NF-κB in gingival epithelial cells while promoting the release of IL-1β, IL-6, and TNF-α. The addition of heat-inactivated B. subtilis R0179 during P. gingivalis infection inhibited the expression of TLR2, TLR4, and p-NF-κB and suppressed the release of IL-1β, IL-6, and TNF-α. In vivo experiments using a mouse model of P. gingivalis-induced experimental periodontitis confirmed these findings, with heat-inactivated B. subtilis R0179 application reducing gingival inflammation, as observed by Hematoxylin and Eosin staining, and downregulating TLR2, TLR4, p-NF-κB, IL-1β, IL-6, and TNF-α signals, as detected by immunohistochemistry. Further investigation using TLR2 and TLR4 agonists revealed that TLR2 receptor agonists antagonized the B. subtilis R0179-induced downregulation of p-NF-κB, IL-6, IL-1β, and TNF-α. These results suggest that B. subtilis R0179 may inhibit P. gingivalis-induced gingival inflammation by suppressing the TLR2/NF-κB signaling pathway, consequently decreasing the production of pro-inflammatory cytokines.
本研究旨在探索热灭活枯草芽孢杆菌(B. subtilis)R0179调节Toll样受体2(TLR2)/核因子κB(NF-κB)信号通路以抑制牙龈卟啉单胞菌(P. gingivalis)诱导的牙龈炎症的机制。体外实验表明,透射电子显微镜观察发现,牙龈卟啉单胞菌在感染后2小时内可侵入牙龈上皮细胞,牙龈卟啉单胞菌感染上调了牙龈上皮细胞中TLR1、TLR2、TLR4、TLR6和磷酸化NF-κB的表达,同时促进白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的释放。在牙龈卟啉单胞菌感染期间添加热灭活的枯草芽孢杆菌R0179可抑制TLR2、TLR4和磷酸化NF-κB的表达,并抑制IL-1β、IL-6和TNF-α的释放。使用牙龈卟啉单胞菌诱导的实验性牙周炎小鼠模型进行的体内实验证实了这些发现,苏木精和伊红染色观察到热灭活的枯草芽孢杆菌R0179应用可减轻牙龈炎症,免疫组织化学检测发现其下调了TLR2、TLR4、磷酸化NF-κB、IL-1β、IL-6和TNF-α信号。使用TLR2和TLR4激动剂的进一步研究表明,TLR2受体激动剂拮抗了枯草芽孢杆菌R0179诱导的磷酸化NF-κB、IL-6、IL-1β和TNF-α的下调。这些结果表明,枯草芽孢杆菌R0179可能通过抑制TLR2/NF-κB信号通路来抑制牙龈卟啉单胞菌诱导的牙龈炎症,从而减少促炎细胞因子的产生。