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氟化钠通过调节自噬来调控根尖乳头干细胞的成骨/成牙分化。

Sodium fluoride regulates the osteo/odontogenic differentiation of stem cells from apical papilla by modulating autophagy.

作者信息

Pan Yin, Li Zehan, Wang Yanqiu, Yan Ming, Wu Jintao, Beharee Romila Gobin, Yu Jinhua

机构信息

Key Laboratory of Oral Diseases of Jiangsu Province, Institute of Stomatology, Nanjing Medical University, Nanjing, Jiangsu, China.

Department of Endodontics, School of Stomatology, Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

J Cell Physiol. 2019 Sep;234(9):16114-16124. doi: 10.1002/jcp.28269. Epub 2019 Feb 14.

Abstract

Fluoride (sodium fluoride) is thought to be essential in the development of tooth, and research shows that fluoride can modulate the differentiation of dental stem cells. However, the effects of fluoride on the committed differentiation of stem cells from apical papilla (SCAPs) and the underlying mechanisms remain unclear. Here, SCAPs were isolated from healthy extracted human third molars with immature roots and then were cultured with NaF conditioned media. Cell Counting Kit-8, EdU staining, and flow cytometry were performed to detected the proliferation activity. Alkaline phosphatase (ALP) activity, Alizarin Red staining, Western blot assay, and real-time reverse-transcription polymerase chain reaction were applied to assess the osteo/odontogenic differentiation NaF-treated SCAPs. Western blot assay and transmission electron microscope were used to evaluate the autophagy involved in the differentiation of SCAPs. ALP activity, ALP protein, and messenger RNA (mRNA) expression showed that 0.5 mM was the optimal concentration for the induction of SCAPs by NaF. 0.5 mM NaF-treated SCAPs induced more mineralized nodules as compared with untreated cells. Moreover, the osteo/odontogenic markers (RUNX2, OSX, DSP, and OCN) in mRNA levels were upregulated while the protein levels of these markers increased considerably in 0.5 mM NaF-treated SCAPs. Furthermore, the autophagy-related proteins (LC3, ATG5, and Beclin1) increased in NaF-treated SCAPs, and the osteo/odontogenic makers significantly decreased while silencing ATG5 to block autophagy. In all, sodium fluoride can regulate the osteo/odontogenic differentiation of SCAPs by modulating autophagy.

摘要

氟化物(氟化钠)被认为在牙齿发育中必不可少,并且研究表明氟化物可以调节牙干细胞的分化。然而,氟化物对根尖乳头干细胞(SCAPs)定向分化的影响及其潜在机制仍不清楚。在此,从具有未成熟牙根的健康拔除的人类第三磨牙中分离出SCAPs,然后用NaF条件培养基进行培养。采用细胞计数试剂盒-8、EdU染色和流式细胞术检测增殖活性。应用碱性磷酸酶(ALP)活性、茜素红染色、蛋白质免疫印迹分析和实时逆转录聚合酶链反应评估经NaF处理的SCAPs的成骨/牙源性分化。采用蛋白质免疫印迹分析和透射电子显微镜评估SCAPs分化过程中的自噬情况。ALP活性、ALP蛋白和信使核糖核酸(mRNA)表达表明,0.5 mM是NaF诱导SCAPs的最佳浓度。与未处理的细胞相比,0.5 mM NaF处理的SCAPs诱导形成更多矿化结节。此外,在0.5 mM NaF处理的SCAPs中,成骨/牙源性标志物(RUNX2、OSX、DSP和OCN)的mRNA水平上调,而这些标志物的蛋白质水平显著增加。此外,自噬相关蛋白(LC3、ATG5和Beclin1)在NaF处理的SCAPs中增加,而沉默ATG5以阻断自噬时,成骨/牙源性标志物显著降低。总之,氟化钠可通过调节自噬来调控SCAPs的成骨/牙源性分化。

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