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牙本质黏结中的10-甲基丙烯酰氧癸基磷酸酯:通过调节牙髓干细胞行为在牙髓保护中的新作用。

10-MDP in dentin bonding: a novel role in pulp protection via modulation of dental pulp stem cell behavior.

作者信息

Ma Yudi, Yang Lu, Gao Yixue, Bian Jingjing, Chen Yinying, Xie Haifeng, Chen Chen

机构信息

Department of Prosthodontics, 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, 1 st Shang-Hai Road, Nanjing, 210029, China.

Department of Stomatology, Xuzhou Central Hospital, Xuzhou Clinical School of Nanjing Medical University, Xuzhou, 221000, China.

出版信息

Clin Oral Investig. 2025 Jun 2;29(6):326. doi: 10.1007/s00784-025-06389-z.

Abstract

OBJECTIVES

10-methacryloyloxydecyl dihydrogen phosphate (10-MDP)-containing adhesives applied to deep dentin cavities near the pulp have demonstrated clinical success without pulp capping. 10-MDP has been reported to exhibit cytotoxic effects on the pulp. However, within the dentin bonding interface, 10-MDP predominantly exists in the form of calcium salts. This study aimed to investigate whether 10-MDP calcium salts exert pulp-protective effects by modulating the biological behavior of dental pulp stem cells (DPSCs).

MATERIALS AND METHODS

Tooth-on-a-chip models were fabricated to evaluate the effects of 10-MDP, HEMA, or their mixture on DPSCs cultured on dentin substrate. 10-MDP calcium salts were synthesized using CaCl and 10-MDP to replicate those formed in dentin surface. The proliferation, migration, apoptosis, odontogenic differentiation, and matrix metalloproteinase (MMP) expression of DPSCs treated with 10-MDP calcium salts, as well as the reactive oxygen species (ROS) levels, mitochondrial morphology, and mitochondrial membrane potential, were determined.

RESULTS

DPSCs incubated with HEMA and 10-MDP mixture showed higher cell viability than when incubated with HEMA alone in tooth-on-a-chip models. 10-MDP calcium salts promoted DPSC proliferation, migration and odontogenic differentiation while suppressing MMP expression. Furthermore, 10-MDP calcium salts reduced ROS levels, maintained mitochondrial morphology and membrane potential in DPSCs, and did not affect apoptosis.

CONCLUSIONS

10-MDP calcium salts exerted beneficial effects on pulp by promoting the odontogenic differentiation, inhibiting the MMP expression, and maintaining mitochondrial dynamics of DPSCs.

CLINICAL RELEVANCE

The application of 10-MDP-containing adhesive has the potential to protect pulp for the formation of 10-MDP calcium salts.

摘要

目的

应用于牙髓附近深龋洞的含10 - 甲基丙烯酰氧基癸基磷酸二氢酯(10 - MDP)的黏结剂在未进行牙髓盖髓的情况下已显示出临床成功。据报道,10 - MDP对牙髓具有细胞毒性作用。然而,在牙本质黏结界面内,10 - MDP主要以钙盐的形式存在。本研究旨在调查10 - MDP钙盐是否通过调节牙髓干细胞(DPSCs)的生物学行为发挥牙髓保护作用。

材料与方法

制作芯片上牙齿模型以评估10 - MDP、甲基丙烯酸羟乙酯(HEMA)或它们的混合物对在牙本质基质上培养的DPSCs的影响。使用氯化钙和10 - MDP合成10 - MDP钙盐,以复制在牙本质表面形成的钙盐。测定用10 - MDP钙盐处理的DPSCs的增殖、迁移、凋亡、牙源性分化和基质金属蛋白酶(MMP)表达,以及活性氧(ROS)水平、线粒体形态和线粒体膜电位。

结果

在芯片上牙齿模型中,与单独用HEMA孵育相比,用HEMA和10 - MDP混合物孵育的DPSCs显示出更高的细胞活力。10 - MDP钙盐促进DPSC增殖、迁移和牙源性分化,同时抑制MMP表达。此外,10 - MDP钙盐降低了DPSCs中的ROS水平,维持了线粒体形态和膜电位,并且不影响凋亡。

结论

10 - MDP钙盐通过促进DPSCs的牙源性分化、抑制MMP表达和维持线粒体动力学对牙髓发挥有益作用。

临床意义

含10 - MDP黏结剂的应用有可能通过形成10 - MDP钙盐来保护牙髓。

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