Suppr超能文献

嗜黏蛋白阿克曼氏菌通过增强细菌清除来减轻牙龈卟啉单胞菌诱导的牙周病。

Akkermansia muciniphila Alleviates Porphyromonas gingivalis-induced Periodontal Disease by Enhancing Bacterial Clearance.

作者信息

Hu Qin, Leung Wai Keung, Acharya Aneesha, Li Xuan, Pelekos George

机构信息

Faculty of Dentistry, The University of Hong Kong, 34 Hospital Road, Sai Ying Pun, Hong Kong SAR, China.

Dr D Y Patil Dental College and Hospital, Pune, India.

出版信息

Probiotics Antimicrob Proteins. 2025 Apr 29. doi: 10.1007/s12602-025-10541-2.

Abstract

This study is to investigate the role of Akkermansia muciniphila (Am) in enhancing immune defense against Porphyromonas gingivalis (Pg)-induced periodontal disease. Twenty C57BL/6 J mice received 50 µL of Pg suspension (1.5 × 10 CFU/mL) with or without 50 µL of Am suspension (1.5 × 10 CFU/mL) orally every 2 days for a total of 18 administrations to assess bone resorption and inflammation. Gingival cervical fluid and periodontal plaques were collected for microbiota analysis using 16S sequencing. THP-1 (a human leukemia monocytic cell line) differentiated macrophages were used to explore the underlying beneficial mechanisms of Am by evaluating gene expression, cytokine production, and phagocytosis activity. Am administration attenuated alveolar bone loss and reduced inflammation in Pg-induced periodontitis in mice. Microbiota analysis revealed that Am reduced bacterial load and modified the composition of periodontal microbiota. In THP-1 macrophages, Am enhanced the phagocytosis of Pg by restoring MyD88 protein levels. RNA sequencing and western blotting results showed that Am upregulated TLR2 and MyD88 expression while downregulating C5aR, indicating interference with the TLR2-C5aR-MyD88 interplay. Am enhances immune defense against Pg-induced periodontal disease by modulating the TLR2-C5aR-MyD88 signaling pathway. These findings suggest that Am could be a promising therapeutic option for managing periodontal disease.

摘要

本研究旨在探讨嗜黏蛋白阿克曼氏菌(Am)在增强对牙龈卟啉单胞菌(Pg)诱导的牙周疾病的免疫防御中的作用。20只C57BL/6 J小鼠每2天口服50 μL Pg悬液(1.5×10⁸ CFU/mL),其中10只同时口服50 μL Am悬液(1.5×10⁸ CFU/mL),共给药18次,以评估骨吸收和炎症情况。收集龈沟液和牙周菌斑,采用16S测序进行微生物群分析。使用THP-1(一种人白血病单核细胞系)分化的巨噬细胞,通过评估基因表达、细胞因子产生和吞噬活性来探索Am潜在的有益机制。给予Am可减轻Pg诱导的小鼠牙周炎中的牙槽骨丢失并减轻炎症。微生物群分析显示,Am降低了细菌载量并改变了牙周微生物群的组成。在THP-1巨噬细胞中,Am通过恢复MyD88蛋白水平增强了对Pg的吞噬作用。RNA测序和蛋白质印迹结果表明,Am上调TLR2和MyD88的表达,同时下调C5aR,表明干扰了TLR2-C5aR-MyD88的相互作用。Am通过调节TLR2-C5aR-MyD88信号通路增强对Pg诱导的牙周疾病的免疫防御。这些发现表明,Am可能是治疗牙周疾病的一种有前景的治疗选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验