牙周炎
医学
细胞生物学
受体
计算生物学
内科学
化学
生物
生物化学
作者
Yuqi Guo,Fangxi Xu,Scott C. Thomas,Yanli Zhang,Benjamin C. Paul,Satish Sakilam,Sungpil Chae,Patty Li,Caleb Almeter,Angela R. Kamer,Paramjit S. Arora,Dana T. Graves,Deepak Saxena,Xin Li
出处
期刊:Cell Reports
[Elsevier]
日期:2022-09-01
卷期号:40 (12): 111389-111389
被引量:6
标识
DOI:10.1016/j.celrep.2022.111389
摘要
Periodontal disease (PD) is one of the most common inflammatory diseases in humans and is initiated by an oral microbial dysbiosis that stimulates inflammation and bone loss. Here, we report an abnormal elevation of succinate in the subgingival plaque of subjects with severe PD. Succinate activates succinate receptor-1 (SUCNR1) and stimulates inflammation. We detected SUCNR1 expression in the human and mouse periodontium and hypothesize that succinate activates SUCNR1 to accelerate periodontitis through the inflammatory response. Administration of exogenous succinate enhanced periodontal disease, whereas SUCNR1 knockout mice were protected from inflammation, oral dysbiosis, and subsequent periodontal bone loss in two different models of periodontitis. Therapeutic studies demonstrated that a SUCNR1 antagonist inhibited inflammatory events and osteoclastogenesis in vitro and reduced periodontal bone loss in vivo. Our study reveals succinate’s effect on periodontitis pathogenesis and provides a topical treatment for this disease.
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