Yoo Yeon Jee, Lee Eun-Hye, Bae Jieun, Kim Woo Jin, Park Chan Ho, Chung Shin Hye, Shon Won Jun, Lee WooCheol, Woo Kyung Mi
Department of Conservative Dentistry, School of Dentistry and Dental Research Institute, Seoul National University, Seoul, 03080, Republic of Korea.
Department of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul, 08826, Republic of Korea.
Mater Today Bio. 2025 Jul 8;33:102062. doi: 10.1016/j.mtbio.2025.102062. eCollection 2025 Aug.
regeneration in restorative dentistry targets the repair of tissues directly at the injury site by utilizing engineered biomaterials to guide endogenous cell activity. This approach aims to simplify treatment procedures and achieve more predictable outcomes, thus to supports the regeneration of damaged tissues and potentially restores tooth vitality, reducing the need for more invasive treatments. This study explores the potential of poly(ε-caprolactone) fibers (PCLF) functionalized with a hypoxia-inducible factor 1-alpha (HIF-1α) stabilizing small molecule dimethyloxalylglycine (DMOG) for regeneration in the context of dental root repair in developing immature teeth. PCLF functionalized with DMOG (PCLF/DMOG) was applied to regenerative endodontic procedure (REP) treatment of infected developing dental roots, and its biologic properties and therapeutic potential were investigated through both studies and experiments, focusing on their capacity to promote regeneration. application demonstrated the effectiveness of PCLF/DMOG in promoting root development, apical closure, and improving infectious lesions, contrasting with contemporary REP treatment controls that showed unpredictable outcomes. Mechanistically, the sustained release of DMOG from PCLF/DMOG significantly enhanced the expression of HIF-1α and upregulated expression of genes associated with angiogenesis and neurogenesis, including VEGF-α and NGF. The PCLF/DMOG upregulated antimicrobial peptides, facilitated efferocytic activities, promoted macrophage polarization to the M2 phenotype, and mobilized mesenchymal stem cells. Taken together, PCLF/DMOG could enhance innate immune responses and foster favorable microenvironment to guide cellular differentiation, promoting regeneration of dental roots in the inflammatory microenvironments.
口腔修复学中的组织再生旨在通过利用工程生物材料引导内源性细胞活性,直接在损伤部位修复组织。这种方法旨在简化治疗程序并实现更可预测的结果,从而支持受损组织的再生,并有可能恢复牙齿活力,减少对更具侵入性治疗的需求。本研究探讨了用缺氧诱导因子1-α(HIF-1α)稳定小分子二甲基草酰甘氨酸(DMOG)功能化的聚(ε-己内酯)纤维(PCLF)在发育中的未成熟牙齿牙根修复中的再生潜力。将用DMOG功能化的PCLF(PCLF/DMOG)应用于感染的发育中牙根的再生性牙髓治疗(REP),并通过研究和实验研究其生物学特性和治疗潜力,重点关注它们促进再生的能力。应用证明了PCLF/DMOG在促进牙根发育、根尖闭合和改善感染性病变方面的有效性,这与当代显示出不可预测结果的REP治疗对照形成对比。从机制上讲,DMOG从PCLF/DMOG中的持续释放显著增强了HIF-1α的表达,并上调了与血管生成和神经发生相关的基因的表达,包括VEGF-α和NGF。PCLF/DMOG上调抗菌肽,促进胞葬作用,促进巨噬细胞向M2表型极化,并动员间充质干细胞。综上所述,PCLF/DMOG可以增强先天免疫反应并营造有利的微环境以引导细胞分化,促进炎症微环境中牙根的再生。