Notch信号通路
赫斯1
细胞生物学
Hes3信号轴
串扰
干细胞
细胞分化
JAG1
信号转导
生物
运行x2
化学
转录因子
遗传学
物理
光学
基因
作者
Feifei Sun,Mei-Hua Wan,Xin Xu,Bo Gao,Yachuan Zhou,Jing Sun,Lei Cheng,Ophir D. Klein,Xuedong Zhou,Liwei Zheng
标识
DOI:10.1177/0022034514531146
摘要
Stem cells from the apical papilla (SCAPs) are important for the formation and regeneration of root dentin. Here, we examined the expression of Notch signaling components in SCAPs and investigated crosstalk between microRNA miR-34aand Notch signaling during cell differentiation. We found that human SCAPs express NOTCH2, NOTCH3, JAG2, DLL3, and HES1, and we tested the relationship between Notch signaling and both cell differentiation and miR-34a expression. NOTCH activation in SCAPs inhibited cell differentiation and up-regulated the expression of miR-34a, whereas miR-34a inhibited Notch signaling in SCAPs by directly targeting the 3′UTR of NOTCH2 and HES1 mRNA and suppressing the expression of NOTCH2, N2ICD, and HES1. DSPP, RUNX2, OSX, and OCN expression was consequently up-regulated. Thus, Notch signaling in human SCAPs plays a vital role in maintenance of these cells. miR-34a interacts with Notch signaling and promotes both odontogenic and osteogenic differentiation of SCAPs.
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