4.7 Article

Cyclic di-AMP Rescues Porphyromonas gingivalis-Aggravated Atherosclerosis

期刊

JOURNAL OF DENTAL RESEARCH
卷 102, 期 7, 页码 785-794

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/00220345231162344

关键词

second-messenger systems; periodontitis; cardiovascular diseases; systemic inflammation; host-pathogen interactions; microbial dysbiosis

向作者/读者索取更多资源

There is a relationship between periodontitis and atherosclerotic cardiovascular diseases, and the periodontal pathogen Porphyromonas gingivalis (Pg) contributes to the progression of atherosclerosis. Cyclic diadenylate monophosphate (c-di-AMP) has been studied as an immune adjuvant and has shown potential in regulating trained immunity. This study aimed to investigate the role of c-di-AMP in Pg-associated atherosclerosis.
Growing evidence demonstrates the relationship between periodontitis and atherosclerotic cardiovascular diseases. The periodontal pathogen Porphyromonas gingivalis (Pg) has been shown to contribute to the progression of atherosclerosis. Cyclic diadenylate monophosphate (c-di-AMP) has been widely studied as an immune adjuvant for tumor immunotherapy, given its ability to activate the stimulator of interferon genes (STING) and regulate trained immunity. This study sought to elucidate the role of c-di-AMP in Pg-associated atherosclerosis. Periodontitis and atherosclerosis mouse models were established by ligature application around maxillary second molars and feeding ApoE knockout mice with a high-fat diet. We found that periodontitis and atherosclerosis were more severe in mice exposed to Pg than mice that underwent ligature placement only, while prophylactic treatment with c-di-AMP activated trained immunity and elicited significant alleviation of alveolar bone resorption, as well as reduced blood lipid levels and atherosclerotic plaque accumulation. After 3 mo of intervention, c-di-AMP limited the elevation of cytokines interleukin (IL)-6, IL-1 beta, tumor necrosis factor a, and interferon beta; extracellular matrix remodeling enzymes MMP-2 and MMP-9; and adhesion molecules ICAM-1 and VCAM-1 gene expression. The mechanism underlying Pg-aggravated atherosclerosis may be attributed to changes in microbiota composition in oral and aortic plaques and excess inflammatory response, whereas c-di-AMP could prevent the effects of Pg infection due to its potential ability to activate trained immunity and regulate microecological balance. Our findings suggest a positive role of c-di-AMP in alleviating Pg-aggravated atherosclerosis by regulating the immune response and influencing the local microenvironment.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据