RvE1 Promotes Axin2+ Cell Regeneration and Reduces Bacterial Invasion

牙髓炎 牙髓(牙) 再生(生物学) 牙髓干细胞 牙科 轴2 根管 牙体牙髓科 细胞生物学 生物 干细胞 医学 信号转导 Wnt信号通路
作者
Yu‐Chiao Wu,Ning Yu,Carla Alvarez Rivas,N. Mehrnia,Alpdoğan Kantarcı,T.E. Van Dyke
出处
期刊:Journal of Dental Research [SAGE Publishing]
卷期号:102 (13): 1478-1487 被引量:8
标识
DOI:10.1177/00220345231197156
摘要

Vital pulp therapy and root canal therapy (RCT) are the dominant treatment for irreversible pulpitis. While the success rate of these procedures is favorable, they have some limitations. For instance, RCT leads to removing significant dentin in the coronal third of the tooth that increases root-fracture risk, which forces tooth removal. The ideal therapeutic goal is dental pulp regeneration, which is not achievable with RCT. Specialized proresolving mediators (SPMs) are well known for inflammatory resolution. The resolution of inflammation and tissue restoration or regeneration is a dynamic and continuous process. SPMs not only have potent immune-modulating functions but also effectively promote tissue homeostasis and regeneration. Resolvins have been shown to promote dental pulp regeneration. The purpose of this study was to explore further the cellular target of Resolvin E1 (RvE1) therapy in dental pulp regeneration and the impact of RvE1 in infected pulps. We investigated the actions of RvE1 on experimentally exposed pulps with or without microbial infection in an Axin2 Cre-Dox ; Ai14 genetically defined mouse model. Our results showed RvE1 promoted Axin2-tdTomato + cell expansion and odontoblastic differentiation after direct pulp capping in the mouse, which we used to mimic reversible pulpitis cases in the clinic. In cultured mouse dental pulp stem cells (mDPSCs), RvE1 facilitated Axin2-tdTomato + cell proliferation and odontoblastic differentiation and also rescued impaired functions after lipopolysaccharide stimulation. In infected pulps exposed to the oral environment for 24 h, RvE1 suppressed inflammatory infiltration, reduced bacterial invasion in root canals, and prevented the development of apical periodontitis, while its proregenerative impact was limited. Collectively, topical treatment with RvE1 facilitated dental pulp regenerative properties by promoting Axin2-expressing cell proliferation and differentiation. It also modulated the resolution of inflammation, reduced infection severity, and prevented apical periodontitis, presenting RvE1 as a novel therapeutic for treating endodontic diseases.
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