Cyclic di-AMP Rescues Porphyromonas gingivalis-Aggravated Atherosclerosis

被引:13
|
作者
Wu, Q. [1 ,2 ,3 ]
Li, Z. [1 ,2 ]
Zhang, Y. [1 ,2 ,3 ]
Luo, K. [1 ,2 ,3 ]
Xu, X. [1 ,2 ,3 ]
Li, J. [1 ,2 ,3 ]
Peng, X. [1 ,2 ,4 ,5 ]
Zhou, X. [1 ,2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp Stomatol, Dept Cariol & Endodont, Chengdu, Peoples R China
[4] Sichuan Univ, West China Hosp Stomatol, State Key Lab Oral Dis, Sect 14 3,Renmin South Rd, Chengdu 610041, Peoples R China
[5] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, Sect 14 3,Renmin South Rd, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
second-messenger systems; periodontitis; cardiovascular diseases; systemic inflammation; host-pathogen interactions; microbial dysbiosis; ORAL INFECTION; PERIODONTITIS; PROTEIN; GROWTH; HEALTH;
D O I
10.1177/00220345231162344
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
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.
引用
收藏
页码:785 / 794
页数:10
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