应用替格鲁西对人类牙髓来源干细胞表达 1 型和 3 型胶原蛋白的影响:初步研究

Pub Date : 2024-09-01 Epub Date: 2024-09-30 DOI:10.4103/njcp.njcp_866_23
C Güler, A M Yilmaz, L Kuru, B Ozen, O B Agrali
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引用次数: 0

摘要

背景:目的:本研究的目的是利用Tideglusib对人牙髓源性干细胞(DPSCs)进行Wnt信号激活,以确定其在胶原蛋白表达方面的潜在功效:从五颗人类第三磨牙智齿牙髓中分离干细胞。方法:从 5 个人类第三磨牙智齿牙髓中分离出干细胞,用 50 nM Tideglusib 处理 24 小时和 1 周,仅在一个样本中鉴定出 DPSCs。通过 Western 印迹分析评估 Axin-2、1 型和 3 型胶原蛋白的表达。未处理的 DPSCs 作为阴性对照。统计分析采用 Mann-Whitney U 检验:结果:24 小时后,试验组 1 型胶原蛋白和 Axin-2 的水平明显高于对照组(分别为 P = 0.000 和 P = 0.001)。与对照组相比,试验组的 3 型胶原蛋白表达在 24 小时后略有增加(P 值 = 0.063)。使用 50 nM Tideglusib 1 周后,1 型和 3 型胶原表达明显减少(P = 0.029,P = 0.038,分别为 0.029 和 0.038)。与此相反,与对照组相比,Axin-2 的水平明显增加(P = 0.000):Tideglusib对DPSCs的应用激活了Wnt信号通路,短期和长期评估中Axin-2的增加证实了这一点,这导致了1型胶原表达在24小时后增加,1周后减少,以及3型胶原表达在1周后减少,这值得进一步研究以评估Tideglusib对细胞外基质表达的影响。
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The Effect of Tideglusib Application on Type 1 and Type 3 Collagen Expressions by Human Dental-Pulp Derived Stem Cells: A Preliminary Study.

Background: Although Tideglusib cytotoxicity studies and its effects on human dental pulp-derived stem cells (DPSCs) have been examined in previous studies, there is no study investigating the expression of type 1 collagen and type 3 collagen by Tideglusib.

Aim: The purpose of this study is to examine the effect of Wnt signaling activation using Tideglusib execution on human DPSC to determine its potential efficacy in collagen expression.

Methods: Stem cell isolation was performed from five human third molar wisdom tooth pulps. DPSCs identified in only one sample were treated with 50 nM Tideglusib for 24 h and 1 week. Axin-2, type 1 and type 3 collagen expressions were evaluated by Western blot analysis. DPSCs without treatment served as a negative control. The Mann-Whitney U test was used for statistical analysis.

Results: The levels of type 1 collagen and Axin-2 in the test group were significantly higher than those in the control group at 24 h (P = 0.000, P = 0.001, respectively). Compared to the control group, a slight increase in type 3 collagen expression was observed in the test group at 24 h (P value = 0.063). Application of 50 nM Tideglusib for 1 week revealed marked decreases in type 1 and type 3 collagen expressions (P = 0.029, P = 0.038, respectively). In contrast, there was a significant increase in the level of Axin-2 (P = 0.000) compared to the control group.

Conclusion: The fact that Wnt signaling pathway activation obtained by Tideglusib application on DPSCs confirmed by the finding in the increase of Axin-2 at short and long-term evaluation periods which is resulted in the increase in the type 1 collagen expression at 24 h and decrease at 1 week together with the decrease in type 3 collagen expression at 1 week warrants further studies to evaluate the effect of Tideglusib on extracellular matrix expression.

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