口腔医学 ›› 2025, Vol. 45 ›› Issue (7): 511-517.doi: 10.13591/j.cnki.kqyx.2025.07.006

• 基础与临床研究 • 上一篇    下一篇

ROS响应型纳米载体用于牙髓炎症的抗氧化治疗

王铭心, 段伊媛, 冯可嘉, 聂晨瑜, 马骞()   

  1. 南京医科大学附属口腔医院综合诊疗科,口腔疾病研究与防治国家级重点实验室培育建设点,江苏省口腔转化医学工程研究中心,江苏南京(210029)
  • 收稿日期:2025-02-08 出版日期:2025-07-28 发布日期:2025-07-24
  • 通讯作者: 马 骞 E-mail:maqian@njmu.edu.cn
  • 基金资助:
    国家自然科学基金(81801029);江苏省卫生健康委科研项目面上项目(M2022060);江苏省科教能力提升工程——江苏省研究型医院(YJXYYJSDW4);江苏省医学创新中心(CXZX202227);南京医科大学大学生创新创业训练计划(202410312046)

A novel ROS-responsive nanocarrier for antioxidant therapy in endodontic inflammation

WANG Mingxin, DUAN Yiyuan, FENG Kejia, NIE Chenyu, MA Qian()   

  1. Department of General Dentistry, The Affiliated Stomatological Hospital of Nanjing Medical University; State Key Laboratory Cultivation Base of Research, Prevention and Treatment for Oral Diseases; Jiangsu Province Engineering Research Center of Stomatological Translational Medicine, Nanjing 210029, China
  • Received:2025-02-08 Online:2025-07-28 Published:2025-07-24

摘要:

目的 探究掺铈介孔生物活性玻璃纳米颗粒(Cerium-containing mesoporous bioactive glass nanoparticles,Ce-MBGNs)作为活性氧(reactive oxygen species,ROS)响应型纳米载体对牙髓炎症的影响,及其促进牙髓干细胞(dental pulp stem cells,DPSCs)成牙本质分化的潜力。方法 CCK-8检测Ce-MBGNs的细胞毒性,RT-qPCR检测其对DPSCs成骨/成牙本质分化相关mRNA以及对RAW264.7炎症因子表达的影响;碱性磷酸酶及茜素红S染色研究其促进牙本质再矿化的能力。免疫荧光及酶标仪检测Ce-MBGNs清除ROS的能力,JC-1染色检测线粒体膜电位。结果 Ce-MBGNs生物相容性良好,可显著提高DPSCs中成骨/成牙本质相关基因表达,促进矿化。同时Ce-MBGNs有效清除细胞内ROS,维持线粒体膜电位,抑制促炎因子表达,促进抗炎因子表达。结论 Ce-MBGNs可以通过维持线粒体膜电位,控制炎症,保护DPSCs免受自身氧化损伤,并促其成牙本质分化,为开发口腔新型治疗药剂提供了理论基础。

关键词: 掺铈介孔生物活性玻璃, 牙髓干细胞, 免疫调节, 成骨/牙本质向分化

Abstract:

Objective To explore the effects of cerium-doped mesoporous bioactive glass nanoparticles (Ce-MBGNs) as reactive oxygen species (ROS)-responsive nanocarriers on inflammation in pulp and their potential to promote odontogenic differentiation of dental pulp stem cells (DPSCs). Methods The cytotoxicity of Ce-MBGNs was assessed by CCK-8. The expression of mRNA of osteogenic/odontogenic differentiation in DPSCs and that of inflammatory factor in RAW264.7 cells were detected by RT-qPCR. Alkaline phosphatase and Alizarin Red S staining were utilized to investigate their ability to promote dentin mineralization. The ability of Ce-MBGNs to scavenge ROS was evaluated by immunofluorescence and JC-1 staining was used to assess the membrane potential (MMP) of mitochondrial. Results Ce-MBGNs exhibited good biocompatibility and significantly increased the expression of osteogenic/odontogenic-related genes in DPSCs, promoting mineralization. Additionally, Ce-MBGNs effectively scavenged intracellular ROS, maintained MMP, inhibited the expression of pro-inflammatory factors, and promoted the expression of anti-inflammatory factors. Conclusion Ce-MBGNs can protect DPSCs from oxidative damage by maintaining the MMP of mitochondrial and controlling inflammation, and promote their odontoblastic differentiation, providing a theoretical basis for the development of novel therapeutic agents for oral treatment.

Key words: Ce-MBGNs, dental pulp stem cells, immunomodulation, osteogenic/odontoblastic differentiation

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