Targeting Hypoxic Pathways for Dental Pulp Regeneration.

IF 3.9 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Shengyan Yang, Waruna Lakmal Dissanayaka
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引用次数: 0

Abstract

Introduction: Introduction: Hypoxia is a critical feature of the dental pulp microenvironment and profoundly influences stem cell behavior and tissue regeneration. Hypoxia-inducible factor 1-alpha (HIF-1α), the master transcription factor governing cellular adaptation to hypoxic stress, plays a pivotal role in coordinating biological processes essential for pulp regeneration. However, the therapeutic potential of targeting HIF-1α signaling in endodontics has not been extensively reviewed.

Methods: A narrative review was conducted using the PubMed and Scopus databases up to August 2025, with search terms related to hypoxia, HIF-1α, dental pulp cells, and pulp regeneration. Laboratory studies investigating hypoxic conditions, HIF-1α manipulation, and their effects on dental pulp cell proliferation, differentiation, and paracrine functions were included in the review.

Results: Hypoxia and HIF-1α activation have been reported to influence the proliferation, odontogenic differentiation, and stemness of dental pulp stem cells, although findings regarding differentiation remain inconsistent across studies. HIF-1α-related signaling appears to modulate the stem cell secretome, including cytokine and extracellular vesicle composition, which may contribute to angiogenesis, neurogenesis, and immunomodulation. Various strategies to target the HIF-1α pathway have been explored for pulp regeneration, including hypoxia preconditioning, hypoxia-mimetic agents, and genetic approaches, with promising but preliminary results.

Conclusions: HIF-1α is a central regulator of pulp regeneration. Strategies targeting HIF-1α signaling offer promising translational opportunities for regenerative endodontic therapies, though optimal protocols, specificity, and long-term safety require further investigation.

针对缺氧途径的牙髓再生。
缺氧是牙髓微环境的一个重要特征,影响着干细胞的行为和组织再生。缺氧诱导因子1- α (HIF-1α)是调控细胞适应缺氧胁迫的主要转录因子,在牙髓再生的生物过程中起着关键的协调作用。越来越多的证据表明,缺氧和HIF-1α激活通过诱导自噬和代谢重编程来促进牙髓干细胞(DPSCs)的增殖和成牙分化。此外,缺氧和hif -1α相关信号调节DPSC分泌组,包括细胞外囊泡组成和自分泌信号,从而支持新生血管和免疫调节。精确调控HIF-1α的表达和活性为促进牙髓组织再生提供了有希望的方法。调控HIF-1α的策略包括转录和翻译控制HIF-1α的表达,抑制脯氨酸羟化酶结构域酶(PHDs)以稳定HIF-1α,以及防止其泛素蛋白酶体介导的降解。因此,治疗干预措施,如缺氧预处理,使用缺氧模拟药物(如去铁胺,二甲基氧基酰甘氨酸),以及针对PHD表达的基因调节已经被探索,以利用缺氧诱导的再生机制。此外,可控氧释放生物材料最近作为一种补充方法出现,以减轻牙髓微环境中的缺氧,提高再生效果。总的来说,这些方法强调了靶向缺氧和HIF-1α信号的潜力,为促进再生牙髓治疗的新药理学、基因和生物材料策略的发展提供了信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of endodontics
Journal of endodontics 医学-牙科与口腔外科
CiteScore
8.80
自引率
9.50%
发文量
224
审稿时长
42 days
期刊介绍: The Journal of Endodontics, the official journal of the American Association of Endodontists, publishes scientific articles, case reports and comparison studies evaluating materials and methods of pulp conservation and endodontic treatment. Endodontists and general dentists can learn about new concepts in root canal treatment and the latest advances in techniques and instrumentation in the one journal that helps them keep pace with rapid changes in this field.
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