Abstract
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 10−7M 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 β-catenin. Results: In total, 26,364 mRNAs were differentially expressed. Comparison of the results of dexamethasone versus control at 2 hours revealed that 7 mRNAs were upregulated and 25 mRNAs were downregulated. The application of dexamethasone reduced the expression of RUNX2 and β-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.
| Original language | English |
|---|---|
| Pages (from-to) | 993-1006 |
| Number of pages | 14 |
| Journal | Journal of International Medical Research |
| Volume | 45 |
| Issue number | 3 |
| DOIs | |
| State | Published - 1 Jun 2017 |
Bibliographical note
Publisher Copyright:© 2017, © The Author(s) 2017.
Keywords
- Dexamethasone
- gingival
- messenger RNA
- stem cells
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