...
首页> 外文期刊>Cell and Tissue Banking >In vitro comparative analysis of cryopreservation of undifferentiated mesenchymal cells derived from human periodontal ligament
【24h】

In vitro comparative analysis of cryopreservation of undifferentiated mesenchymal cells derived from human periodontal ligament

机译:冻存人牙周膜未分化间充质细胞的体外比较分析

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Cryopreservation aims to cease all biological functions of living tissues in a reversible and controlled manner, i.e., to permit the recovery of cells by maintaining a high degree of their viability and functional integrity. The objective of this study was to evaluate in vitro the influence of cryopreservation on undifferentiated mesenchymal cells derived from the periodontal ligament of human third molars. Mesenchymal cells were isolated from six healthy teeth and cultured in α-MEM medium supplemented with antibiotics and 15% FBS in a humid atmosphere with 5% CO2 at 37°C. The cells isolated from each tooth were divided into two groups: group I (fresh, non-cryopreserved cells) was immediately cultured, and group II was submitted to cryopreservation for 30 days. The rates of cell adhesion and proliferation were analyzed in the two groups by counting the cells adhered to the wells at 24, 48 and 72 h after plating. The number of cells per well was obtained by counting viable cells in a hemocytometer using the Trypan blue exclusion method. Differences between groups at each time point were evaluated by the Wilcoxon test. The Friedman test was used to determine differences between time points and, if detected, the Wilcoxon test with Bonferroni correction was applied. The results showed no significant difference in the in vitro growth capacity of undifferentiated mesenchymal cells between the two groups. In conclusion, cryopreservation for 30 days had no influence on periodontal ligament mesenchymal cells.
机译:冷冻保存旨在以可逆和可控的方式终止活组织的所有生物学功能,即通过维持高度的活力和功能完整性来恢复细胞。这项研究的目的是在体外评估冷冻保存对人类第三磨牙的牙周膜衍生的未分化间充质细胞的影响。从六颗健康的牙齿中分离出间充质细胞,并在37%的潮湿环境中,在含有5%CO 2 的潮湿环境中,在添加了抗生素和15%FBS的α-MEM培养基中进行培养。从每颗牙齿中分离出的细胞分为两组:第一组(新鲜,未冷冻保存的细胞)立即培养,第二组进行低温保存30天。通过计数接种后24、48和72小时粘附在孔上的细胞,分析两组细胞的粘附和增殖速率。通过使用台盼蓝排除法在血细胞计数器中计数活细胞来获得每孔的细胞数。通过Wilcoxon检验评估各时间点组之间的差异。弗里德曼检验用于确定时间点之间的差异,并且如果检测到,则应用具有Bonferroni校正的Wilcoxon检验。结果显示两组之间未分化的间充质细胞的体外生长能力没有显着差异。总之,冷冻保存30天对牙周膜间充质细胞没有影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号