Crucial Triad in Pulp-Dentin Complex Regeneration: Dental Stem Cells, Scaffolds, and Signaling Molecules

F. Sandra, A. Sutanto, Widya Wulandari, Reynaldo Lambertus, M. Celinna, Nurrani Mustika Dewi, S. Ichwan
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Abstract

BACKGROUND: Pulp damage can lead to dentinogenesis impairment, irreversible pulpitis, or pulp necrosis. Despite being the most used endodontic procedure to treat damaged pulp, root canal therapy only results in nonvital teeth which are prone to fractures and secondary infection. Pulp-dentin regeneration has a potential to regenerate structure similar to normal pulp-dentin complex, and can be achieved by combining dental stem cells, scaffold, and signaling molecules. This article reviews the role of various types of dental stem cells, scaffolds, signaling molecules, and their combinations in regenerating pulp-dentin complex.CONTENT: Dental pulp stem cell (DPSC), stem cell from human exfoliated deciduous teeth (SHED), and dental follicle stem cell (DFSC) were reported to regenerate pulp-dentin complex in situ. SHED might be more promising than DPSCs and DFSCs for regenerating pulp-dentin complex, since SHED have a higher proliferation potential and higher expression levels of signaling molecules. Scaffolds have characteristics resembling extracellular matrix, thus providing a suitable microenvironment for transplanted dental stem cells. To accelerate the regeneration process, exogenous signaling molecules are often delivered together with dental stem cells. Scaffolds and signaling molecules have different regenerative potential, including induction of cell proliferation and migration, formation of pulp- and/or dentin-like tissue, as well as angiogenesis and neurogenesis promotion.SUMMARY: Combinations of dental stem cells, scaffold, and signaling molecules are important to achieve the functional pulp-dentin complex formation. Current trends and future directions on regenerative endodontics should be explored. The right combination of dental stem cells, scaffold, and signaling molecules could be determined based on the patients’ characteristics. Incomplete pulp-dentin regeneration could be overcome by applying dental stem cells, scaffold, and/or signaling molecules in multiple visits.KEYWORDS: pulp-dentin regeneration, regenerative endodontics, dental stem cells, scaffold, signaling molecules
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牙髓-牙本质复合体再生中的关键三元:牙干细胞、支架和信号分子
背景:牙髓损伤可导致牙本质发育障碍、不可逆牙髓炎或牙髓坏死。尽管根管治疗是治疗受损牙髓最常用的方法,但根管治疗只会导致非重要牙齿容易骨折和继发感染。牙髓-牙本质再生具有再生类似于正常牙髓-牙本质复合体结构的潜力,可以通过结合牙髓干细胞、支架和信号分子来实现。本文综述了各类牙干细胞、支架、信号分子及其组合在牙髓-牙本质复合体再生中的作用。内容:据报道,牙髓干细胞(DPSC)、人脱落乳牙干细胞(SHED)和牙泡干细胞(DFSC)可以原位再生牙髓-牙本质复合体。由于SHED具有更高的增殖潜能和更高的信号分子表达水平,因此它可能比DPSCs和DFSCs更有希望再生牙髓-牙本质复合体。支架具有类似细胞外基质的特性,为移植牙干细胞提供了适宜的微环境。为了加速牙干细胞的再生过程,外源信号分子通常与牙干细胞一起传递。支架和信号分子具有不同的再生潜能,包括诱导细胞增殖和迁移,形成牙髓和/或牙本质样组织,以及促进血管生成和神经发生。摘要:牙干细胞、支架和信号分子的结合对于实现功能性牙本质复合体的形成至关重要。再生牙髓学的发展趋势和未来发展方向有待探讨。牙干细胞、支架和信号分子的正确组合可以根据患者的特点来确定。牙髓-牙本质再生不完全可以通过多次就诊应用牙髓干细胞、支架和/或信号分子来克服。关键词:牙本质再生,再生牙髓学,牙干细胞,支架,信号分子
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