| Literature DB >> 24710391 |
F Sun1, M Wan2, X Xu3, B Gao3, Y Zhou4, J Sun1, L Cheng1, O D Klein5, X Zhou1, L Zheng6.
Abstract
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. © International & American Associations for Dental Research.Entities:
Keywords: cell fate determination; epigenetic; microRNA; stem cells from apical papilla; tooth development; tooth regeneration
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Year: 2014 PMID: 24710391 DOI: 10.1177/0022034514531146
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116