首页> 外文期刊>Journal of periodontal research >Cellular responses of rat periodontal ligament cells under hypoxia and re-oxygenation conditions in vitro.
【24h】

Cellular responses of rat periodontal ligament cells under hypoxia and re-oxygenation conditions in vitro.

机译:体外低氧和复氧条件下大鼠牙周膜细胞的细胞反应。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

BACKGROUND AND OBJECTIVE: The aim of this study was to investigate the responses of periodontal ligament cells under hypoxia and re-oxygenation conditions in vitro. MATERIAL AND METHODS: Periodontal ligament fibroblasts were isolated from rat incisors. In the hypoxia group, cells were incubated in 2% O(2) for 1-3 d. In the re-oxygenation group, cells were first incubated under the same conditions as the hypoxia group for 24 h and then were returned to normoxic conditions and cultured for 1-2 additional days. RESULTS: Proliferation ratios increased in all groups in a time-dependent manner. Proliferation ratios in both the hypoxia and re-oxygenation groups were significantly higher than in the control group on days 2 and 3. Alkaline phosphatase activity was significantly higher in the hypoxia group than in the control and the re-oxygenation groups. The expression of bone sialoprotein mRNA was significantly higher in the hypoxia group than in the control group on days 1 and 2. The expression of vascular endothelial growth factor mRNA was significantly higher in the hypoxia group than in the control group on days 1 and 2. In the re-oxygenation group, the level of expression of bone sialoprotein mRNA and vascular endothelial growth factor mRNA were similar to those of the control group. The expression of heat shock protein 70 mRNA in the hypoxia group was similar to that in the control group, whereas in the re-oxygenation group it was statistically higher than in the other groups. CONCLUSION: These results suggest that periodontal ligament cells maintain their osteogenic ability in hypoxia and re-oxygenation conditions in vitro.
机译:背景与目的:本研究旨在探讨缺氧和复氧条件下牙周膜细胞的体外反应。材料与方法:从大鼠切牙中分离出牙周膜成纤维细胞。在缺氧组中,将细胞在2%O(2)中孵育1-3天。在再充氧组中,首先将细胞在与缺氧组相同的条件下孵育24小时,然后恢复至常氧条件,再培养1-2天。结果:所有组的增殖率均呈时间依赖性。在第2天和第3天,缺氧和复氧组的增殖率均显着高于对照组。缺氧组的碱性磷酸酶活性明显高于对照组和复氧组。低氧组在第1、2天的骨唾液蛋白mRNA表达明显高于对照组。低氧组在第1、2天的血管内皮生长因子mRNA表达明显高于对照组。在复氧组中,骨唾液蛋白mRNA和血管内皮生长因子mRNA的表达水平与对照组相似。低氧组中热休克蛋白70 mRNA的表达与对照组相似,而复氧组中的热休克蛋白70 mRNA的表达高于其他组。结论:这些结果表明牙周膜细胞在体外缺氧和复氧条件下仍能保持其成骨能力。

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