Effects of Deferoxamine on the Repair Ability of Dental Pulp Cells In Vitro

被引:26
作者
Jiang, Long [1 ]
Peng, Wei-Wei [1 ]
Li, Li-Fen [1 ]
Du, Rong [1 ]
Wu, Tian-Tian [1 ]
Zhou, Zhuo-Jun [1 ]
Zhao, Jun-Jun [1 ]
Yang, Ya [1 ]
Qu, Dong-Lin [1 ]
Zhu, Ya-Qin [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Dept Gen Dent, Shanghai Key Lab Stomatol,Peoples Hosp 9, Shanghai 200011, Peoples R China
基金
中国国家自然科学基金;
关键词
Deferoxamine; dental pulp cells; hypoxia-inducible factors-1 alpha; repair ability; HYPOXIA-INDUCIBLE FACTORS; STEM-CELLS; TRICALCIUM SILICATE; GENE-EXPRESSION; IRON CHELATION; PROLIFERATION; DIFFERENTIATION; DESFERRIOXAMINE; MINERALIZATION; REGENERATION;
D O I
10.1016/j.joen.2013.12.016
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: In previous studies, we found that hypoxia promoted the mineralization of dental pulp cells (DPCs). However, the clinical application of hypoxia as a therapy is questionable or unfeasible. Deferoxamine (DFO), a medication for iron overload, has also been shown to induce hypoxia. The purpose of this study was to investigate the effects of DFO on the repair ability of DPCs. Methods: DPCs were obtained by using a tissue explant technique in vitro and were treated with different concentrations of DFO or hypoxia culture for 2 days. The viability, proliferation, migration, and odontogenic differentiation of DPCs were assayed and analyzed. The expression of hypoxia-inducible factor 1-alpha (HIF-1 alpha) was assessed through Western blotting. Results: Ten micromolars of DFO enhanced the expression of HIF-1 alpha similarly to hypoxia and did not affect the viability of DPCs for 2 days. Furthermore, the proliferation, migration, and odontogenic differentiation of DPCs were promoted by DFO. Conclusions: These results suggest that DFO might improve the repair ability of DPCs by HIF-1 alpha.
引用
收藏
页码:1100 / 1104
页数:5
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