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Updated: Feb 22, 2026
Author Spotlight: Enhancing Dental Pulp Research with Improved Mouse Models
Published on: October 27, 2023
Pulpitis Transiently Affect Hepatic Bone Morphogenetic Protein 9 Expression by Lipopolysaccharide
Tianzhu Song1, Dongzhe Song2, Yanglin Zeng3
1State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China; Key Laboratory of Oral Diseases of Gansu Province Key & Laboratory of Stomatology of State Ethnic Affairs Commission, Northwest Minzu University, Lanzhou, Gansu, China.
Introduction And Aims:
The connection between oral and systemic diseases is receiving increasing attention. Pulpitis is an infectious disease, and its potential impact on the systemic system deserves further investigation.
Methods:
A rat/mouse pulpitis model was utilized to explore the variations in bone morphogenetic protein 9 (BMP9) and lipopolysaccharide (LPS) concentrations within liver tissue and blood. Hepatic stellate cells were cultivated and subsequently stimulated with LPS. Histone H3K9 methylation and associated methyltransferase levels were quantified. G9a function was investigated by the G9a methyltransferase inhibitor UNC0642.
Results:
In rats and mice with pulpitis, BMP9 expression initially declined in both the liver and blood, followed by a subsequent increase. This BMP9 trend in LPS-stimulated hepatic stellate cells mirrored the findings observed in vivo. Mechanistically, the involvement of H3K9 dimethylation and G9a methyltransferase in this process was elucidated. Treatment with UNC0642 successfully restored suppressed BMP9 levels. Chromatin immunoprecipitation assays further confirmed an increased enrichment of H3K9 dimethylation in the promoter region of the BMP9 gene following LPS stimulation of mouse hepatic stellate cells.
Conclusion:
These findings suggested that LPS in pulpitis might transiently influence the expression of BMP9 in liver tissues, and pulpitis might have potential effects on systemic tissues and organs.
Clinical Relevance:
This study provides a proof-of-concept for targeting epigenetic pathways to mitigate the oral-systemic disease link, motivating future clinical trials in high-risk populations.
