School of Medicine, South China University of Technology, Guangzhou, China.
Cell Biochem Biophys. 2024 Jun;82(2):535-547. doi: 10.1007/s12013-024-01274-0. Epub 2024 May 7.
Mesenchymal stem cells (MSCs) from dental pulp (DP-MSCs), which include dental pulp stem cells (DPSCs) isolated from permanent teeth and stem cells from human exfoliated deciduous teeth (SHED), have emerged as highly promising cell sources for tissue regeneration, due to their high proliferative rate, multi-lineage differentiation capability and non-invasive accessibility. DP-MSCs also exert extensive paracrine effects through the release of extracellular vesicles (EVs) and multiple trophic factors. To be noted, the microenvironment, commonly referred to as the stem cell niche, plays a crucial role in shaping the functionality and therapeutic effects of DP-MSCs, within which hypoxia has garnered considerable attention. Extensive research has demonstrated that hypoxic conditions profoundly impact DP-MSCs. Specifically, hypoxia promotes DP-MSC proliferation, survival, stemness, migration, and pro-angiogenic potential while modulating their multi-lineage differentiation capacity. Furthermore, hypoxia stimulates the paracrine activities of DP-MSCs, leading to an increased production of EVs and soluble factors. Considering these findings, hypoxia preconditioning has emerged as a promising approach to enhance the therapeutic potential of DP-MSCs. In this comprehensive review, we provide a systematic overview of the influence of hypoxia on DP-MSCs, shedding light on the underlying mechanisms involved. Moreover, we also discuss the potential applications of hypoxia-preconditioned DP-MSCs or their secretome in tissue regeneration. Additionally, we delve into the methodologies employed to simulate hypoxic environments. This review aims to promote a comprehensive and systematic understanding of the hypoxia-induced effects on DP-MSCs and facilitate the refinement of regenerative therapeutic strategies based on DP-MSCs.
牙髓间充质干细胞(DP-MSCs),包括从恒牙中分离的牙髓干细胞(DPSCs)和人脱落乳牙中的干细胞(SHED),由于其高增殖率、多向分化能力和非侵入性可及性,已成为组织再生极具前景的细胞来源。DP-MSCs 还通过释放细胞外囊泡(EVs)和多种营养因子发挥广泛的旁分泌作用。需要注意的是,微环境,通常被称为干细胞巢,在塑造 DP-MSCs 的功能和治疗效果方面起着至关重要的作用,其中缺氧引起了相当大的关注。大量研究表明,缺氧条件对 DP-MSCs 有深远影响。具体而言,缺氧促进 DP-MSC 的增殖、存活、干性、迁移和促血管生成潜力,同时调节其多向分化能力。此外,缺氧刺激 DP-MSCs 的旁分泌活性,导致 EVs 和可溶性因子的产生增加。鉴于这些发现,缺氧预处理已成为增强 DP-MSCs 治疗潜力的一种有前途的方法。在这篇全面的综述中,我们系统地概述了缺氧对 DP-MSCs 的影响,揭示了其中涉及的潜在机制。此外,我们还讨论了缺氧预处理的 DP-MSCs 或其分泌组在组织再生中的潜在应用。此外,我们还深入探讨了模拟缺氧环境所采用的方法。本综述旨在促进对 DP-MSCs 缺氧诱导效应的全面和系统理解,并促进基于 DP-MSCs 的再生治疗策略的完善。