Key Laboratory of Oral Diseases of Jiangsu Province, Stomatological Institute of Nanjing Medical University, Nanjing, Jiangsu, China.
Endodontic Department, School of Stomatology, Nanjing Medical University, Nanjing, Jiangsu, China.
Cell Prolif. 2018 Dec;51(6):e12485. doi: 10.1111/cpr.12485. Epub 2018 Aug 2.
OBJECTIVES: Oestrogen receptor (ER) is a common nucleus receptor that is essential for the regulation of cell growth, proliferation and differentiation. This study was to examine whether ERα can affect the proliferation and odonto/osteogenic differentiation of stem cells from apical papilla (SCAPs). MATERIALS AND METHODS: Stem cells from apical papillas were isolated, purified and then transfected with ERα lentiviruses. The proliferation capacity was investigated by cell counting kit-8 (CCK-8) assay and flow cytometry. The odonto/osteogenic differentiation ability was analysed by alkaline phosphatase (ALP) activity, alizarin red staining, western blot assay (WB) and real-time RT-PCR. MAPK pathway and its downstream transcriptional factors were explored by WB assay. RESULTS: As indicated by CCK-8 assay and flow cytometry, ERα had no significant effect on the proliferation of SCAPs. When ERα was overexpressed, the ALP activity and the formation of calcified nodules were significantly enhanced in SCAPs. Moreover, the odonto/osteogenic markers (DMP1/DMP1, DSPP/DSP, RUNX2/RUNX2, OCN/OCN) in SCAPs were significantly up-regulated at both mRNA and protein levels. On the contrary, the odonto/osteogenic differentiation ability of SCAPs was remarkably inhibited after suppression of ERα. Mechanistically, the protein levels of phosphorylated ERK and JNK significantly increased after ERα overexpression. Moreover, some downstream transcriptional factors of MAPK pathway were simultaneously activated by ERα overexpression. CONCLUSIONS: Together, the data accumulated here indicated that ERα can enhance the odonto/osteogenic differentiation of SCAPs via ERK and JNK MAPK pathways.
目的:雌激素受体(ER)是一种常见的核受体,对于细胞生长、增殖和分化的调节至关重要。本研究旨在探讨 ERα 是否能影响根尖乳头干细胞(SCAPs)的增殖和牙/骨向分化能力。
材料和方法:分离、纯化 SCAPs 并转染 ERα 慢病毒。通过细胞计数试剂盒-8(CCK-8)检测和流式细胞术检测增殖能力。通过碱性磷酸酶(ALP)活性、茜素红染色、Western blot 检测(WB)和实时 RT-PCR 分析牙/骨向分化能力。通过 WB 检测探讨 MAPK 通路及其下游转录因子。
结果:CCK-8 检测和流式细胞术结果表明,ERα 对 SCAPs 的增殖没有显著影响。当 ERα 过表达时,SCAPs 的 ALP 活性和钙化结节形成明显增强。此外,SCAPs 中的牙/骨向标志物(DMP1/DMP1、DSPP/DSP、RUNX2/RUNX2、OCN/OCN)在 mRNA 和蛋白水平上均显著上调。相反,抑制 ERα 后,SCAPs 的牙/骨向分化能力明显受到抑制。从机制上讲,过表达 ERα 后,磷酸化 ERK 和 JNK 的蛋白水平显著增加。此外,过表达 ERα 还同时激活了 MAPK 通路的一些下游转录因子。
结论:综上所述,这些数据表明 ERα 通过 ERK 和 JNK MAPK 通路增强 SCAPs 的牙/骨向分化能力。
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