首页> 外文会议>Academic Committee conference of Shanghai key lab of stomatology >Hypoxia Promotes Mineralization of Human Dental Pulp Cells
【24h】

Hypoxia Promotes Mineralization of Human Dental Pulp Cells

机译:低氧促进人类牙髓细胞矿化

获取原文

摘要

Introduction: Dental pulp can be exposed to hypoxic conditions in case of trauma or inflammation. Dental pulp cells (DPCs) have mineralization potential, which plays a key role in pulp repair and reparative dentino-genesis process. Little information is available about DPC mineralization in hypoxic condition. The purpose of this study was to assess the influence of hypoxia on DPC mineralization to pave the way for a better understanding of dental pulp regeneration and reparative dentin formation. Methods: Human DPCs were obtained by using tissue explant technique in vitro and cultured in normoxia (20% O2) or hypoxia (5% O2). Cell viability was investigated by methyl-thiazol-tetrazolium assay. Cell mineralization was assessed by von Kossa staining and alizarin red S staining. Important mineral genes such as osteocalcin (OCN), dentin matrix acidic phosphoprotein-1 (DMP-1), bone sialoprotein (BSP), and dentin sialophosphoprotein (DSPP) were determined by real-time polymerase chain reaction. Results: Cell viability of DPCs increased more in hypoxia than in normoxia from day 3 to day 5. Von Kossa staining and alizarin red S staining showed DPCs in hypoxia had higher mineralization activity than in normoxia. Expression of mRNAs for OCN, DMP-1, BSP, and DSPP was greater in hypoxia than in normoxia. Conclusions: These results imply that hypoxia promotes DPC mineralization.
机译:简介:如果发生外伤或发炎,牙髓可能会缺氧。牙髓细胞(DPC)具有矿化潜力,在牙髓修复和修复性牙本质发生过程中起关键作用。关于缺氧条件下DPC矿化的信息很少。这项研究的目的是评估缺氧对DPC矿化的影响,从而为更好地了解牙髓再生和修复性牙本质的形成铺平道路。方法:采用组织外植体技术体外获得人DPC,并在常氧(20%O2)或低氧(5%O2)中培养。通过甲基噻唑-四唑鎓测定法研究细胞活力。通过von Kossa染色和茜素红S染色评估细胞的矿化。通过实时聚合酶链反应确定了重要的矿物质基因,如骨钙蛋白(OCN),牙本质基质酸性磷蛋白1(DMP-1),骨唾液蛋白(BSP)和牙本质唾液磷蛋白(DSPP)。结果:在缺氧的第3天到第5天,DPCs的细胞活力比正常氧增加更多。VonKossa染色和茜素红S染色显示缺氧时DPC的矿化活性高于常氧。在低氧条件下,OCN,DMP-1,BSP和DSPP的mRNA表达高于常氧状态。结论:这些结果暗示缺氧促进DPC矿化。

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