聚脱氧核糖核酸对人牙周韧带细胞作为撕脱牙储存介质的作用

Sang Tae Ro, Y. Chae, Koeun Lee, Mi Sun Kim, O. Nam, Hyo-seol Lee, S. Choi
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引用次数: 0

摘要

目的:评价聚脱氧核糖核苷酸(PDRN)作为脱脱牙保存介质的适用性。材料与方法:采用细胞计数试剂盒-8 (Cell Counting Kit-8)和活/死法检测储存在Hank’s平衡盐溶液和PDRN溶液(浓度分别为10、25、50和100 μg/mL)和自来水中的人牙周韧带(PDL)细胞的活力。此外,采用一氧化氮检测和定量实时聚合酶链反应(qRT-PCR)评价PDRN的抗炎作用。结果:100 μg/mL PDRN溶液中保存的PDL细胞活力显著高于其他溶液(p < 0.01);此外,与HBSS相比,100 μg/mL PDRN溶液中储存的细胞显著降低了NO的产生(p < 0.0001), 50和100 μg/mL PDRN溶液中储存的细胞表达的肿瘤坏死因子α、白细胞介素(IL) -4、IL-6和IL-10的水平显著降低(p < 0.01)。结论:PDRN溶液对PDL细胞具有保细胞和抗炎作用。本研究结果可作为进一步实验的基础,旨在开发有效的撕脱牙储存介质。
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Effect of Polydeoxyribonucleotide on Human Periodontal Ligament Cells as a Storage Medium for Avulsed Tooth
Objective: This study aimed to evaluate the suitability of polydeoxyribonucleotides (PDRN) as a storage medium for avulsed teeth.Materials and Methods: The viability of human periodontal ligament (PDL) cells stored in Hank’s balanced salt solution and PDRN solutions (concentrations, 10, 25, 50, and 100 μg/mL) and tap water was measured using the Cell Counting Kit-8 and Live/Dead assays. In addition, Nitric oxide detection and quantitative real-time polymerase chain reaction (qRT-PCR) were performed to evaluate the anti-inflammatory effect of PDRN.Results: The viability of PDL cells stored in a 100 μg/mL PDRN solution was significantly higher than that of cells stored in the other solutions (p < 0.01). Furthermore, cells stored in 100 μg/mL PDRN solution demonstrated a significantly reduced NO production (p < 0.0001), and cells stored in 50 and 100 μg/mL PDRN solutions expressed significantly lower levels of tumor necrosis factor α, interleukin (IL) -4, IL-6, and IL-10 (p < 0.01) compared to cells stored in HBSS.Conclusion: The PDRN solution exhibited cell-preserving and anti-inflammatory effects on the PDL cells. The findings of this study can serve as a basis for further experiments directed at the development of an effective storage medium for avulsed teeth.
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