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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。

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

作者信息

Ramenzoni Liza L, Weber Franz E, Attin Thomas, Schmidlin Patrick R

机构信息

Clinic of Preventive Dentistry, Periodontology and Cariology, Center of Dental Medicine, University of Zurich, Plattenstrasse 11, 8032 Zurich, Switzerland.

Oral Biotechnology and Bioengineering, Division of Cranio-Maxilo-Facial and Oral Surgery, Center of Dental Medicine, University of Zurich, Plattenstrasse 11, 8032 Zurich, Switzerland.

出版信息

Materials (Basel). 2017 May 24;10(6):573. doi: 10.3390/ma10060573.

Abstract

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%, / %) 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 , and were analyzed by RT-PCR ( < 0.05, -test). The viability proliferation increased at 1- and 5-min exposures for all CeCl₃ concentrations, in contrast to no treatment ( < 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 , and 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.

摘要

本研究调查了氯化铈(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暴露于三种不同浓度的CeCl₃溶液(1%、5%和10%,/ %)中,持续三种不同的时间(1、5和10分钟)。暴露于CeCl₃ 72小时后,通过MTT试验评估细胞活力。划痕试验测定细胞迁移情况以及在24小时时测量的伤口宽度。通过RT-PCR分析细胞周期蛋白 、 和 的基因表达模式( < 0.05, -检验)。与未处理组相比,所有CeCl₃浓度在暴露1分钟和5分钟时活力增殖增加(24小时时 < 0.05)。10分钟后未发现CeCl₃有影响。划痕试验显示,在5%和10%的浓度下,24小时后1分钟和5分钟时细胞迁移增加高达60%。细胞周期蛋白 、 和 均显示上调,证实细胞增殖增加。本研究表明,CeCl₃的暴露时间和浓度可能对成纤维细胞活力和迁移有积极影响。在不同的牙周治疗中,如有必要,应用CeCl₃作为细胞刺激剂可能有利于导致治疗性组织纤维化或牙齿周围更具抗性的组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8670/5552080/e626759d2698/materials-10-00573-g001.jpg

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