MiR-146a-5p Promotes Dental Stem Cells Osteo/odontogenic Differentiation through NF-Kappa B Signaling Pathway by Targeting TRAF6.

Xin Yu, Jian Feng Lu, Mei Qin Gao, Bin Xiong, Wen Qian Xia
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引用次数: 1

Abstract

Objective: To screen miRNAs that could simultaneously regulate osteo/odontogenic differentiation of multiple stem cells, including dental pulp stem cells (DPSCs), stem cells from the apical papilla (SCAPs) and periodontal ligament stem cells (PDLSCs).

Methods: Differentially expressed miRNAs analysis on three miRNA microarrays data of dental stem cells undergoing osteo/odontogenic differentiation (GSE138180, GSE154466 and GSE159508) was performed, and miR-146a-5p were identified by bioinformatic prediction, dual-luciferase reporter assay and quantitative real-time polymerase chain reaction (PCR). In addition, differentially expressed genes between miR-146a-5p overexpressed group and control group (GSE79341) were applied for KEGG pathways enrichment analysis.

Results: MiR-146a-5p expression increased in the osteo/odontogenic differentiation of DPSCs, SCAPs and PDLSCs. Tumour necrosis factor receptor (TNFR)-associated factor 6 (TRAF6) was identified as the target gene of miR-146a-5p. Furthermore, miR-146a-5p could influence the NF-Kappa B signalling pathway.

Conclusion: This study suggests that miR-146a-5p could promote differentiation in multiple dental stem cells through the NF-Kappa B signalling pathway by targeting TRAF6.

MiR-146a-5p通过NF-Kappa B信号通路靶向TRAF6促进牙干细胞成骨/成牙分化
目的:筛选能同时调控牙髓干细胞(DPSCs)、根尖乳头干细胞(SCAPs)和牙周韧带干细胞(PDLSCs)等多种干细胞成骨/牙源性分化的miRNAs。方法:对骨/牙源性分化牙干细胞(GSE138180、GSE154466和GSE159508)的三个miRNA微阵列数据进行差异表达miRNAs分析,并通过生物信息学预测、双荧光素酶报告基因法和实时定量聚合酶链反应(PCR)鉴定miR-146a-5p。此外,应用miR-146a-5p过表达组与对照组的差异表达基因(GSE79341)进行KEGG通路富集分析。结果:MiR-146a-5p在DPSCs、SCAPs和PDLSCs成骨/牙源性分化过程中表达升高。肿瘤坏死因子受体(TNFR)相关因子6 (TRAF6)被确定为miR-146a-5p的靶基因。此外,miR-146a-5p可能影响NF-Kappa B信号通路。结论:本研究提示miR-146a-5p可通过NF-Kappa B信号通路靶向TRAF6促进多种牙干细胞分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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