Ma Yudi, Yang Lu, Gao Yixue, Bian Jingjing, Chen Yinying, Xie Haifeng, Chen Chen
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.
Clin Oral Investig. 2025 Jun 2;29(6):326. doi: 10.1007/s00784-025-06389-z.
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).
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.
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.
10-MDP calcium salts exerted beneficial effects on pulp by promoting the odontogenic differentiation, inhibiting the MMP expression, and maintaining mitochondrial dynamics of DPSCs.
The application of 10-MDP-containing adhesive has the potential to protect pulp for the formation of 10-MDP calcium salts.
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。
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。
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。
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。
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。