Author:
Hou Jingyi,Xu Junji,Liu Yi,Zhang Haiping,Wang Sihan,Jiao Yao,Guo Lijia,Li Song
Abstract
Abstract
Background
Butyrate is a major subgingival microbial metabolite that is closely related to periodontal disease. It affects the proliferation and differentiation of mesenchymal stem cells. However, the mechanisms by which butyrate affects the osteogenic differentiation of periodontal ligament stem cells (PDLSCs) remain unclear. Here, we investigated the effect of sodium butyrate (NaB) on the osteogenic differentiation of human PDLSCs.
Methods
PDLSCs were isolated from human periodontal ligaments and treated with various concentrations of NaB in vitro. The cell counting kit-8 assay and flow cytometric analysis were used to assess cell viability. The osteogenic differentiation capabilities of PDLSCs were evaluated using the alkaline phosphatase activity assay, alizarin red staining, RT-PCR, western blotting and in vivo transplantation.
Results
NaB decreased PDLSC proliferation and induced apoptosis in a dose- and time-depend manner. Additionally, 1 mM NaB reduced alkaline phosphatase activity, mineralization ability, and the expression of osteogenic differentiation-related genes and proteins. Treatment with a free fatty acids receptor 2 (FFAR2) antagonist and agonist indicated that NaB inhibited the osteogenic differentiation capacity of PDLSCs by affecting the expression of Smad1.
Conclusion
Our findings suggest that NaB inhibits the osteogenic differentiation of PDLSCs by activating FFAR2 and decreasing the expression of Smad1.
Funder
National Natural Science Foundation of China
Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support
Beijing Baiqianwan Talents Project
Beijing Municipal Administration of Hospitals’ Ascent Plan
Beijing Municipal Science & Technology Commission
Beijing Municipal Administration of Hospitals’ Youth Programme
Innovation Foundation of Beijing Stomatological Hospital
Publisher
Springer Science and Business Media LLC
Cited by
6 articles.
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