Cargando…

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

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 concentrati...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Bo-Bae, Kim, Minji, Park, Yun-Hee, Ko, Youngkyung, Park, Jun-Beom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536397/
https://www.ncbi.nlm.nih.gov/pubmed/28459354
http://dx.doi.org/10.1177/0300060517701035
Descripción
Sumario: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 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.