Department of Materials Science and Technology, University of Crete, 70013 Heraklion, Greece.
Department of Prosthodontics, School of Dentistry, Faculty of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Int J Mol Sci. 2023 Mar 30;24(7):6465. doi: 10.3390/ijms24076465.
This study aims to investigate the impact of kappa-carrageenan on dental pulp stem cells (DPSCs) behavior in terms of biocompatibility and odontogenic differentiation potential when it is utilized as a component for the production of 3D sponge-like scaffolds. For this purpose, we prepared three types of scaffolds by freeze-drying (i) kappa-carrageenan/chitosan/gelatin enriched with KCl (KCG-KCl) as a physical crosslinker for the sulfate groups of kappa-carrageenan, (ii) kappa-carrageenan/chitosan/gelatin (KCG) and (iii) chitosan/gelatin (CG) scaffolds as a control. The mechanical analysis illustrated a significantly higher elastic modulus of the cell-laden scaffolds compared to the cell-free ones after 14 and 28 days with values ranging from 25 to 40 kPa, showing an increase of 27-36%, with the KCG-KCl scaffolds indicating the highest and CG the lowest values. Cell viability data showed a significant increase from days 3 to 7 and up to day 14 for all scaffold compositions. Significantly increasing alkaline phosphatase (ALP) activity has been observed over time in all three scaffold compositions, while the KCG-KCl scaffolds indicated significantly higher calcium production after 21 and 28 days compared to the CG control. The gene expression analysis of the odontogenic markers DSPP, ALP and RunX2 revealed a two-fold higher upregulation of DSPP in KCG-KCl scaffolds at day 14 compared to the other two compositions. A significant increase of the RunX2 expression between days 7 and 14 was observed for all scaffolds, with a significantly higher increase of at least twelve-fold for the kappa-carrageenan containing scaffolds, which exhibited an earlier ALP gene expression compared to the CG. Our results demonstrate that the integration of kappa-carrageenan in scaffolds significantly enhanced the odontogenic potential of DPSCs and supports dentin-pulp regeneration.
本研究旨在探讨κ-卡拉胶作为一种成分,用于生产 3D 海绵状支架时,对牙髓干细胞(DPSCs)的生物相容性和牙向分化潜能的影响。为此,我们通过冷冻干燥制备了三种支架:(i)κ-卡拉胶/壳聚糖/明胶中富含 KCl(KCG-KCl),作为κ-卡拉胶硫酸基团的物理交联剂,(ii)κ-卡拉胶/壳聚糖/明胶(KCG)和(iii)壳聚糖/明胶(CG)支架作为对照。力学分析表明,与不含细胞的支架相比,细胞负载支架在 14 天和 28 天后的弹性模量显著提高,范围在 25 到 40kPa 之间,增加了 27-36%,其中 KCG-KCl 支架的弹性模量最高,CG 支架的弹性模量最低。细胞活力数据显示,所有支架组成物的细胞存活率从第 3 天到第 7 天,再到第 14 天均有显著增加。所有三种支架组成物的碱性磷酸酶(ALP)活性随时间的推移均呈显著增加,而 KCG-KCl 支架在第 21 天和第 28 天的钙产量明显高于 CG 对照组。牙向分化标志物 DSPP、ALP 和 RunX2 的基因表达分析显示,在第 14 天,KCG-KCl 支架中 DSPP 的上调幅度是其他两种组成物的两倍。所有支架的 RunX2 表达在第 7 天到第 14 天之间均显著增加,至少增加了 12 倍,κ-卡拉胶含量较高的支架增加幅度更大,ALP 基因表达也早于 CG 支架。我们的结果表明,κ-卡拉胶在支架中的整合显著增强了 DPSCs 的牙向分化潜能,支持牙本质-牙髓再生。