Short-term application of dexamethasone on stem cells derived from human gingiva reduces the expression of RUNX2 and β-catenin

被引:9
作者
Kim, Bo-Bae [1 ]
Kim, Minji [1 ]
Park, Yun-Hee [2 ]
Ko, Youngkyung [1 ]
Park, Jun-Beom [1 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Periodont, Seoul, South Korea
[2] Ebiogen, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Dexamethasone; gingival; messenger RNA; stem cells; OSTEOBLASTIC DIFFERENTIATION; RNA-SEQ; PROLIFERATION; MUTATIONS; MICRORNA; RECEPTOR; PATHWAY; BIOLOGY; GENE; PULP;
D O I
10.1177/0300060517701035
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective Next-generation sequencing was performed to evaluate the effects of short-term application of dexamethasone on human gingiva-derived mesenchymal stem cells. Methods Human gingiva-derived stem cells were treated with a final concentration of 10(-7)M dexamethasone and the same concentration of vehicle control. This was followed by mRNA sequencing and data analysis, gene ontology and pathway analysis, quantitative real-time polymerase chain reaction of mRNA, and western blot analysis of RUNX2 and -catenin. Results In total, 26,364mRNAs were differentially expressed. Comparison of the results of dexamethasone versus control at 2 hours revealed that 7mRNAs were upregulated and 25mRNAs were downregulated. The application of dexamethasone reduced the expression of RUNX2 and -catenin in human gingiva-derived mesenchymal stem cells. Conclusion The effects of dexamethasone on stem cells were evaluated with mRNA sequencing, and validation of the expression was performed with qualitative real-time polymerase chain reaction and western blot analysis. The results of this study can provide new insights into the role of mRNA sequencing in maxillofacial areas.
引用
收藏
页码:993 / 1006
页数:14
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