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Cerium Chloride Application Promotes Wound Healing and Cell Proliferation in Human Foreskin Fibroblasts

机译:氯化铈的应用促进人包皮成纤维细胞的伤口愈合和细胞增殖

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摘要

This study investigated the effect of cerium chloride (CeCl3) on cell migration and gene expression of human foreskin fibroblasts (HFF). HFF were exposed to three different CeCl3 solutions (1%, 5% and 10%, w/v %) for three different time durations (1, 5 and 10 min). 72 h after exposure to CeCl3, cell viability was assessed by MTT test. A scratch-wounded assay determined the cell migration and the width of the wound, measured at 24 h. Gene expression patterns for cyclins B1, D1 and E1 were analyzed by RT-PCR (p < 0.05, t-test). The viability proliferation increased at 1- and 5-min exposures for all CeCl3 concentrations, in contrast to no treatment (p < 0.05 at 24 h). No influence of CeCl3 was found after 10 min. The scratch assay showed increased cell migration up to 60% at 1 and 5 min after 24 h at 5% and 10%. Cyclin B1, D1 and E1 all showed upregulation, confirming an increase in cell proliferation. This study demonstrates that exposure time and concentration of CeCl3 may have a positive effect on fibroblast viability and migration. Application of CeCl3 may be beneficial as a cell-stimulating agent leading to therapeutic tissue fibrosis or more resistant tissue around teeth, when warranted, during different periodontal therapies.
机译:这项研究调查了氯化铈(CeCl3)对人包皮成纤维细胞(HFF)细胞迁移和基因表达的影响。将HFF暴露于三种不同的CeCl3溶液(1%,5%和10%,w / v%)中,持续三个不同的持续时间(1、5和10分钟)。暴露于CeCl3 72小时后,通过MTT测试评估细胞活力。划痕试验测定了24小时测量的细胞迁移和伤口宽度。通过RT-PCR分析细胞周期蛋白B1,D1和E1的基因表达模式(p <0.05,t检验)。与未处理的情况相比,所有CeCl3浓度下暴露1分钟和5分钟后,活力增殖均增加(24小时时p <0.05)。 10分钟后未发现CeCl3的影响。刮擦试验显示,在24小时后的1和5分钟,细胞迁移率分别为5%和10%时高达60%。细胞周期蛋白B1,D1和E1均显示上调,证实细胞增殖增加。这项研究表明,暴露时间和CeCl3浓度可能对成纤维细胞的活力和迁移有积极影响。必要时,在不同的牙周治疗期间,使用CeCl3作为细胞刺激剂可能会有益,从而导致治疗性组织纤维化或牙齿周围更具抵抗力的组织。

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