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氧化石墨烯量子点的浓度依赖性细胞摄取通过AMPK/mTOR途径促进牙髓细胞的成牙本质细胞分化。

Concentration-Dependent Cellular Uptake of Graphene Oxide Quantum Dots Promotes the Odontoblastic Differentiation of Dental Pulp Cells via the AMPK/mTOR Pathway.

作者信息

Lin Ling, Zheng Yexin, Wang Chao, Li Pei, Xu Duoling, Zhao Wei

机构信息

Hospital of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou 510055, China.

出版信息

ACS Omega. 2023 Feb 1;8(6):5393-5405. doi: 10.1021/acsomega.2c06508. eCollection 2023 Feb 14.

Abstract

As zero-dimension nanoparticles, graphene oxide quantum dots (GOQDs) have broad potential for regulating cell proliferation and differentiation. However, such regulation of dental pulp cells (DPSCs) with different concentrations of GOQDs is insufficiently investigated, especially on the molecular mechanism. The purpose of this study was to explore the effect and molecular mechanism of GOQDs on the odontoblastic differentiation of DPSCs and to provide a theoretical basis for the repair of pulp vitality by pulp capping. CCK-8, immunofluorescence staining, alkaline phosphatase activity assay and staining, alizarin red staining, qRT-PCR, and western blotting were used to detect the proliferation and odontoblastic differentiation of DPSC coculturing with different concentrations of GOQDs. The results indicate that the cellular uptake of low concentration of GOQDs (0.1, 1, and 10 μg/mL) could promote the proliferation and odontoblastic differentiation of DPCSs. Compared with other concentration groups, 1 μg/mL GOQDs show better ability in such promotion. In addition, with the activation of the AMPK signaling pathway, the mTOR signaling pathway was inhibited in DPSCs after coculturing with GOQDs, which indicates that low concentrations of GOQDs could regulate the odontoblastic differentiation of DPSCs by the AMPK/mTOR signaling pathway.

摘要

作为零维纳米颗粒,氧化石墨烯量子点(GOQDs)在调节细胞增殖和分化方面具有广阔的潜力。然而,不同浓度的GOQDs对牙髓细胞(DPSCs)的这种调节作用尚未得到充分研究,尤其是在分子机制方面。本研究的目的是探讨GOQDs对DPSCs成牙本质细胞分化的影响及其分子机制,为盖髓术修复牙髓活力提供理论依据。采用CCK-8、免疫荧光染色、碱性磷酸酶活性测定及染色、茜素红染色、qRT-PCR和蛋白质免疫印迹法检测不同浓度GOQDs与DPSC共培养时的增殖和成牙本质细胞分化情况。结果表明,低浓度的GOQDs(0.1、1和10μg/mL)被细胞摄取后可促进DPCSs的增殖和成牙本质细胞分化。与其他浓度组相比,1μg/mL的GOQDs在促进作用方面表现更佳。此外,与GOQDs共培养后,DPSCs中的mTOR信号通路受到抑制,同时AMPK信号通路被激活,这表明低浓度的GOQDs可通过AMPK/mTOR信号通路调节DPSCs的成牙本质细胞分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e4f/9933470/a708b6ef696d/ao2c06508_0002.jpg

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