Dental Pulp Stem Cells: Advances to Applications.

IF 1.7 Q4 CELL BIOLOGY
Stem Cells and Cloning-Advances and Applications Pub Date : 2020-02-13 eCollection Date: 2020-01-01 DOI:10.2147/SCCAA.S166759
Takeo W Tsutsui
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引用次数: 77

Abstract

Dental pulp stem cells (DPSCs) have a high capacity for differentiation and the ability to regenerate a dentin/pulp-like complex. Numerous studies have provided evidence of DPSCs' differentiation capacity, such as in neurogenesis, adipogenesis, osteogenesis, chondrogenesis, angiogenesis, and dentinogenesis. The molecular mechanisms and functions of DPSCs' differentiation process are affected by growth factors and scaffolds. For example, growth factors such as basic fibroblast growth factor (bFGF), transforming growth factor-β (TGF-β), nerve growth factor (NGF), platelet-derived growth factor (PDGF), and bone morphogenic proteins (BMPs) influence DPSC fate, including in differentiation, cell proliferation, and wound healing. In addition, several types of scaffolds, such as collagen, hydrogel, decellularized bioscaffold, and nanofibrous spongy microspheres, have been used to characterize DPSC cellular attachment, migration, proliferation, differentiation, and functions. An appropriate combination of growth factors and scaffolds can enhance the differentiation capacity of DPSCs, in terms of optimizing not only dental-related expression but also dental pulp morphology. For a cell-based clinical approach, focus has been placed on the tissue engineering triad [cells/bioactive molecules (growth factors)/scaffolds] to characterize DPSCs. It is clear that a deep understanding of the mechanisms of stem cells, including their aging, self-renewal, microenvironmental homeostasis, and differentiation correlated with cell activity, the energy for which is provided from mitochondria, should provide new approaches for DPSC research and therapeutics. Mitochondrial functions and dynamics are related to the direction of stem cell differentiation, including glycolysis, oxidative phosphorylation, mitochondrial metabolism, mitochondrial transcription factor A (TFAM), mitochondrial elongation, and mitochondrial fusion and fission proteins. This review summarizes the effects of major growth factors and scaffolds for regenerating dentin/pulp-like complexes, as well as elucidating mitochondrial properties of DPSCs for the development of advanced applications research.

牙髓干细胞:应用进展。
牙髓干细胞(DPSCs)具有较高的分化能力和再生牙本质/牙髓样复合体的能力。大量研究已经证明了DPSCs在神经发生、脂肪形成、成骨、软骨形成、血管生成和牙本质发生等方面的分化能力。DPSCs分化过程的分子机制和功能受生长因子和支架的影响。例如,碱性成纤维细胞生长因子(bFGF)、转化生长因子-β (TGF-β)、神经生长因子(NGF)、血小板衍生生长因子(PDGF)和骨形态发生蛋白(BMPs)等生长因子影响DPSC的命运,包括分化、细胞增殖和伤口愈合。此外,几种类型的支架,如胶原蛋白、水凝胶、脱细胞生物支架和纳米纤维海绵状微球,已被用于表征DPSC细胞的附着、迁移、增殖、分化和功能。生长因子与支架的适当组合可以增强DPSCs的分化能力,不仅可以优化牙体相关表达,还可以优化牙髓形态。对于基于细胞的临床方法,重点放在组织工程三位一体(细胞/生物活性分子(生长因子)/支架)来表征DPSCs。很明显,对干细胞机制的深入了解,包括它们的衰老、自我更新、微环境稳态和与细胞活性相关的分化,线粒体提供的能量,应该为DPSC的研究和治疗提供新的方法。线粒体的功能和动力学与干细胞分化方向有关,包括糖酵解、氧化磷酸化、线粒体代谢、线粒体转录因子A (TFAM)、线粒体伸长、线粒体融合和裂变蛋白等。本文综述了主要生长因子和支架在牙本质/牙髓样复合体再生中的作用,并阐明了DPSCs的线粒体特性,为其进一步的应用研究奠定了基础。
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
CiteScore
6.50
自引率
0.00%
发文量
10
审稿时长
16 weeks
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