Department of Endodontics, Stomatological Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China; Department of Medical Laboratory, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, Guangdong 510515, China.
Department of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong 510515, China.
Arch Oral Biol. 2021 Nov;131:105265. doi: 10.1016/j.archoralbio.2021.105265. Epub 2021 Sep 20.
Sodium fluoride (NaF) plays an important role in preventing dental caries. However, the regulatory effect of NaF on the committed differentiation of DPSCs is not fully understood. In this study, we characterized the impact of micromolar levels of NaF on the osteo/odontogenic differentiation of DPSCs.
DPSCs were isolated from healthy human third molars and were cultured in conditioned media with different concentrations of NaF. RNA sequencing (RNA-seq) combined with Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis was used to assess the pathways regulated by NaF. Alkaline phosphatase activity, Alizarin red staining, Western blotting, and real-time qRT-PCR were used to determine the osteo/odontogenic differentiation in DPSCs treated with NaF.
NaF significantly promoted the osteo/odontogenic differentiation of DPSCs at micromolar levels. Furthermore, RNA-seq and KEGG pathway enrichment analysis indicated that the PI3K/AKT pathway was involved in the pro-osteoclastogenesis effect of NaF. Western blotting analysis exhibited that the phosphorylation of AKT was decreased in NaF-treated DPSCs. Chemical inhibition of the PI3K/AKT pathway abrogated the NaF-promoted DPSCs osteo/odontogenic differentiation.
Micromolar NaF can promote the osteo/odontogenic differentiation of DPSCs by inhibiting the PI3K/AKT pathway.
The data used to support the findings of this study are available from the corresponding author upon request.
氟化钠(NaF)在预防龋齿方面起着重要作用。然而,NaF 对牙髓细胞定向分化的调节作用尚不完全清楚。本研究旨在研究纳摩尔浓度的 NaF 对牙髓细胞成骨/成牙本质分化的影响。
从健康人第三磨牙中分离牙髓细胞,并在不同浓度 NaF 的条件培养基中培养。采用 RNA 测序(RNA-seq)联合京都基因与基因组百科全书通路富集分析评估 NaF 调节的通路。碱性磷酸酶活性、茜素红染色、Western blot 和实时 qRT-PCR 用于检测 NaF 处理的牙髓细胞的成骨/成牙本质分化。
纳摩尔浓度的 NaF 可显著促进牙髓细胞的成骨/成牙本质分化。此外,RNA-seq 和 KEGG 通路富集分析表明,PI3K/AKT 通路参与了 NaF 促进破骨细胞形成的作用。Western blot 分析显示,NaF 处理的牙髓细胞中 AKT 的磷酸化水平降低。化学抑制 PI3K/AKT 通路可阻断 NaF 促进牙髓细胞成骨/成牙本质分化。
纳摩尔浓度的 NaF 可通过抑制 PI3K/AKT 通路促进牙髓细胞的成骨/成牙本质分化。
本研究支持的数据可应要求向通讯作者获取。