Back to Search Start Over

Periodontitis exacerbates atherosclerosis through Fusobacterium nucleatum-promoted hepatic glycolysis and lipogenesis.

Authors :
Zhou, Lu-Jun
Lin, Wen-Zhen
Meng, Xiao-Qian
Zhu, Hong
Liu, Ting
Du, Lin-Juan
Bai, Xue-Bing
Chen, Bo-Yan
Liu, Yan
Xu, Yuanzhi
Xie, Yufeng
Shu, Rong
Chen, Fa-Ming
Zhu, Ya-Qin
Duan, Sheng-Zhong
Source :
Cardiovascular Research. 6/15/2023, Vol. 119 Issue 8, p1706-1717. 12p.
Publication Year :
2023

Abstract

Aims Positive associations between periodontitis (PD) and atherosclerosis have been established, but the causality and mechanisms are not clear. We aimed to explore the causal roles of PD in atherosclerosis and dissect the underlying mechanisms. Methods and results A mouse model of PD was established by ligation of molars in combination with application of subgingival plaques collected from PD patients and then combined with atherosclerosis model induced by treating atheroprone mice with a high-cholesterol diet (HCD). PD significantly aggravated atherosclerosis in HCD-fed atheroprone mice, including increased en face plaque areas in whole aortas and lesion size at aortic roots. PD also increased circulating levels of triglycerides and cholesterol, hepatic levels of cholesterol, and hepatic expression of rate-limiting enzymes for lipogenesis. Using 16S ribosomal RNA (rRNA) gene sequencing, Fusobacterium nucleatum was identified as the most enriched PD-associated pathobiont that is present in both the oral cavity and livers. Co-culture experiments demonstrated that F. nucleatum directly stimulated lipid biosynthesis in primary mouse hepatocytes. Moreover, oral inoculation of F. nucleatum markedly elevated plasma levels of triglycerides and cholesterol and promoted atherogenesis in HCD-fed ApoE −/− mice. Results of RNA-seq and Seahorse assay indicated that F. nucleatum activated glycolysis, inhibition of which by 2-deoxyglucose in turn suppressed F. nucleatum -induced lipogenesis in hepatocytes. Finally, interrogation of the molecular mechanisms revealed that F. nucleatum -induced glycolysis and lipogenesis by activating PI3K/Akt/mTOR signalling pathway in hepatocytes. Conclusions PD exacerbates atherosclerosis and impairs lipid metabolism in mice, which may be mediated by F. nucleatum -promoted glycolysis and lipogenesis through PI3K/Akt/mTOR signalling in hepatocytes. Treatment of PD and specific targeting of F. nucleatum are promising strategies to improve therapeutic effectiveness of hyperlipidaemia and atherosclerosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00086363
Volume :
119
Issue :
8
Database :
Academic Search Index
Journal :
Cardiovascular Research
Publication Type :
Academic Journal
Accession number :
169792560
Full Text :
https://doi.org/10.1093/cvr/cvad045