The Effect of Simvastatin on Odontoblastic Differentiation of Human Dental Pulp Stem Cells: An In Vitro Study.

IF 3.1 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Carmela Del Giudice, Flavia Iaculli, Carlo Rengo, Alessandro Salucci, Gianrico Spagnuolo, Francesco Riccitiello, Maurizio Bossù, Antonella Polimeni, Gianni Di Giorgio
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Abstract

Objectives: The aim of the current in vitro study was to assess the effect of simvastatin on the early-stage differentiation of human dental pulp stem cells (hDPSCs) in an odontogenic pattern by evaluating the expression of specific odontogenic-related genes. Methods: hDPSCs were cultured in the presence of different concentrations of simvastatin (0.1, 0.5, 1, 5, and 10 µM) to evaluate cytotoxicity. Moreover, osteogenic differentiation was assessed by Alkaline Phosphatase (ALP) activity and alizarin red staining (ARS) after 7 days of culture. Finally, odontogenic-related gene (OCN, MEPE, DSPP, and DMP-1) expression analysis was performed. Results: Three days after treatment, higher concentrations of simvastatin (1, 5, and 10 µM) significantly limited cell viability. Upregulation of ALP activity and odontoblastic cell-related genes (OCN and MEPE) was observed in the presence of 1 µM simvastatin. The expression was statistically higher for ALP (p = 0.0001) and OCN (p = 0.0231). On the other hand, comparable or slightly less effect concerning mineralization ability with respect to the control group, as well as in the expression of DSPP and DMP-1, was observed. Conclusions: Simvastatin demonstrated a positive influence on dentinogenesis by improving the expression of specific markers such as MEPE and OCN. However, its effect on inflammation reduction and the potential to be used in combination with other materials should be further assessed. Simvastatin might be successfully applied in the regeneration of damaged dental pulp tissues and promotion of reparative dentinogenesis. Additional studies should be carried out to support the obtained outcomes.

辛伐他汀对人牙髓干细胞成牙细胞分化影响的体外研究
目的:本实验旨在通过评价辛伐他汀对人牙髓干细胞(hDPSCs)成牙相关基因表达的影响,探讨辛伐他汀对人牙髓干细胞(hDPSCs)成牙模式早期分化的影响。方法:采用不同浓度辛伐他汀(0.1、0.5、1、5、10µM)培养hDPSCs,评价其细胞毒性。培养7天后,采用碱性磷酸酶(ALP)活性和茜素红染色(ARS)评价成骨分化程度。最后进行牙源性相关基因(OCN、MEPE、DSPP、DMP-1)表达分析。结果:治疗3天后,高浓度辛伐他汀(1、5和10µM)显著限制细胞活力。在1µM辛伐他汀存在下,观察到ALP活性和成牙细胞相关基因(OCN和MEPE)的上调。ALP (p = 0.0001)和OCN (p = 0.0231)的表达有统计学意义。另一方面,与对照组相比,在矿化能力以及DSPP和DMP-1的表达方面,观察到类似或略低的影响。结论:辛伐他汀通过改善MEPE和OCN等特异性标志物的表达,对牙本质形成有积极影响。然而,其消炎效果和与其他材料联合使用的潜力有待进一步评估。辛伐他汀可成功应用于损伤牙髓组织的再生和牙本质修复。应该进行更多的研究来支持所获得的结果。
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
Dentistry Journal
Dentistry Journal Dentistry-Dentistry (all)
CiteScore
3.70
自引率
7.70%
发文量
213
审稿时长
11 weeks
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