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日用化学工业(中英文) ›› 2026, Vol. 56 ›› Issue (10): 1362-1370.doi: 10.3969/j.issn.2097-2806.2026.10.009

• 开发与应用 • 上一篇    下一篇

基于TLR2信号通路探究裂褶菌β-葡聚糖对口腔上皮细胞炎症的调控作用

林宇城,周菲,刘青,卢伊娜*()   

  1. 上海珈凯生物股份有限公司 技术创新中心, 上海 201507
  • 收稿日期:2025-12-19 修回日期:2026-09-14 出版日期:2026-10-22 发布日期:2026-10-30

A β-glucan from Schizophyllum commune attenuates Fusobacterium nucleatum-induced inflammatory responses in oral epithelial cells via TLR2 signaling

Yucheng Lin,Fei Zhou,Qing Liu,Yina Lu*()   

  1. Technology Innovation Center, JAKA Biotech Co., Ltd., Shanghai 201507, China
  • Received:2025-12-19 Revised:2026-09-14 Online:2026-10-22 Published:2026-10-30
  • Contact: E-mail: inna_lu@jakabiotech.com

摘要:

裂褶菌β-葡聚糖(Gioactive SPG-PF)是一种以β- (1→3)葡聚糖为主链、β- (1→6)葡萄糖为侧链的天然微生物多糖,具有抗氧化与抗炎等多种活性,但其在口腔微环境中的作用机制尚未明确。为此,该研究从分子与细胞层面探究Gioactive SPG-PF是否可通过TLR2通路调控口腔上皮细胞的炎症反应,为将其开发为口腔舒缓新原料提供理论依据。通过建立灭活具核梭杆菌(Fusobacterium nucleatum)诱导的TR146细胞炎症模型,评估了Gioactive SPG-PF的口腔舒缓功效。结果显示,Gioactive SPG-PF可剂量依赖性地显著抑制IL-6和IL-8的蛋白分泌,并下调TLR2、IL6和IL8的基因表达。进一步的分子对接分析表明,Gioactive SPG-PF的单糖(n=1)和二糖(n=2)重复单元能以较高亲和力与TLR2蛋白活性位点结合,其结合模式与TLR2经典抑制剂CU-CPT22相似。综上,Gioactive SPG-PF可有效抑制口腔上皮细胞的炎症反应,其作用机制可能与调控TLR2信号通路有关,该研究为其作为新型口腔舒缓原料的开发提供了理论支持。

关键词: Gioactive SPG-PF, 具核梭杆菌, TLR2, 炎症, 分子对接

Abstract:

Schizophyllum commune β-glucan (Gioactive SPG-PF) is a natural microbial polysaccharide characterized by a β- (1→3) -glucan backbone with β- (1→6) -glucose side chains, known for its antioxidant and anti-inflammatory activities. However, its mechanism of action within the oral microenvironment remains unclear. This study aimed to investigate whether Gioactive SPG-PF can regulate inflammatory responses in oral epithelial cells via the TLR2 pathway, thereby providing a theoretical basis for its development as a novel oral soothing ingredient. An inflammatory model was established using TR146 cells stimulated with inactivated Fusobacterium nucleatum, and the anti-inflammatory effects of Gioactive SPG-PF was evaluated. The results show that Gioactive SPG-PF exhibits significant dose-dependent inhibition of IL-6 and IL-8 protein secretion, and downregulates the transcriptional expression of TLR2, IL6, and IL8 genes. Further molecular docking analysis indicates that the monosaccharide (n=1) and disaccharide (n=2) repeating units of Gioactive SPG-PF can bind with high affinity to the active site of the TLR2 protein, exhibiting a binding mode similar to that of the classical TLR2 inhibitor CU-CPT22. In conclusion, Gioactive SPG-PF effectively suppresses inflammatory responses in oral epithelial cells, potentially through the modulation of the TLR2 signaling pathway, providing experimental and theoretical support for its development as a new oral soothing ingredient.

Key words: Gioactive SPG-PF, Fusobacterium nucleatum, TLR2, inflammation, molecular docking

中图分类号: 

  • TQ658