Department of Dentistry, Charles University, Faculty of Medicine in Hradec Kralove and University Hospital Hradec Kralove, 500 05 Hradec Kralove, Czech Republic.
Department of Histology and Embryology, Faculty of Medicine in Hradec Kralove, Charles University, 500 03 Hradec Kralove, Czech Republic.
Int J Mol Sci. 2021 Apr 23;22(9):4432. doi: 10.3390/ijms22094432.
Dental pulp stem cells (DPSCs) are a type of easily accessible adult mesenchymal stem cell. Due to their ease of access, DPSCs show great promise in regenerative medicine. However, the tooth extractions from which DPSCs can be obtained are usually performed at a period of life when donors would have no therapeutic need of them. For this reason, it is imperative that successful stem cell storage techniques are employed so that these cells remain viable for future use. Any such techniques must result in high post-thaw stem cell recovery without compromising stemness, proliferation, or multipotency. Uncontrolled-rate freezing is not a technically or financially demanding technique compared to expensive and laborious controlled-rate freezing techniques. This study was aimed at observing the effect of uncontrolled-rate freezing on DPSCs stored for 6 and 12 months. Dimethyl sulfoxide at a concentration of 10% was used as a cryoprotective agent. Various features such as shape, proliferation capacity, phenotype, and multipotency were studied after DPSC thawing. The DPSCs did not compromise their stemness, viability, proliferation, or differentiating capabilities, even after one year of cryopreservation at -80 °C. After thawing, they retained their stemness markers and low-level expression of hematopoietic markers. We observed a size reduction in recovery DPSCs after one year of storage. This observation indicates that DPSCs can be successfully used in potential clinical applications, even after a year of uncontrolled cryopreservation.
牙髓干细胞(DPSCs)是一种易于获得的成体间充质干细胞。由于其易于获得,DPSCs 在再生医学中具有很大的应用前景。然而,从这些牙齿中提取 DPSCs 通常是在捐赠者没有治疗需求的生命阶段进行的。因此,必须采用成功的干细胞储存技术,以确保这些细胞在未来仍具有活力。任何此类技术都必须在不损害干细胞特性、增殖能力或多能性的情况下,实现高的冻存后干细胞回收率。与昂贵且繁琐的控制速率冷冻技术相比,非控制速率冷冻在技术和经济上都不是一项具有挑战性的技术。本研究旨在观察非控制速率冷冻对储存 6 个月和 12 个月的 DPSCs 的影响。使用 10%浓度的二甲亚砜作为冷冻保护剂。在 DPSC 解冻后,研究了其形态、增殖能力、表型和多能性等各种特征。即使在 -80°C 下进行一年的低温保存,DPSCs 也没有损害其干细胞特性、活力、增殖或分化能力。解冻后,它们保留了其干细胞标志物和低水平的造血标志物表达。我们观察到在储存一年后回收的 DPSCs 体积减小。这一观察结果表明,即使经过一年的非控制冷冻保存,DPSCs 也可以成功用于潜在的临床应用。