The regenerative potential of Tideglusib and CHIR99021 small molecules as potent odontogenic differentiation enhancers of human dental pulp stem cells

• Published in: Clinical oral investigations Vol. 28; no. 1; p. 48
• Main Authors: Hanna, Samer, Eldeen, Ghada Nour, Alfayate, Ruth Perez, Aly, Riham
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 28.12.2023; Springer Nature B.V
• Subjects: Antigens, Differentiation; beta Catenin; Cbfa-1 protein; Dental Pulp; Dentistry; Flow cytometry; Humans; Medicine; Molars; Odontology; Polymerase chain reaction; Regeneration; Statistical analysis; Stem Cells; Wnt protein; β-Catenin; Dentin; Regeneration; Dental pulp capping; AXIN2; Wnt/β-catenin signalling pathway; GSK-3 inhibitor
• ISSN: 1436-3771; 1432-6981; 1436-3771
• DOI: 10.1007/s00784-023-05452-x

Objectives To assess the effect of Tideglusib and CHIR99021 small molecules on the odontogenic differentiation potential of human dental pulp stem cells (hDPSCs) via Wnt/β-catenin pathway activation. Methodology hDPSCs were isolated from impacted third molars indicated for extraction and were characterized by flow cytometry. hDPSCs were then induced to differentiate into odontogenic lineage in the presence of Tideglusib and CHIR99021. Odontogenic differentiation was evaluated using Alizarin Red stain and RT-PCR for expression of odontogenic specific differentiation markers: DSPP, DMP1, ALP, OPN, and RUNX2 in relation to undifferentiated cells. RT-PCR was also conducted to assess the expression of Wnt/β-catenin pathway activation marker (AXIN2). One-way ANOVA Kruskal-Wallis test was used for statistical analysis. Results Wnt/β-catenin pathway was successfully activated by Tideglusib and CHIR99021 in hDPSCs where AXIN2 was significantly upregulated. Successful odontogenic differentiation was confirmed by Alizarin Red staining of calcified nodules. RT-PCR for odontogenic differentiation markers DSPP, DMP1, and RUNX expression by hDPSCs induced by CHIR99021 was higher than that expressed by hDPSCs induced by Tideglusib, whereas expression of OPN and ALP was higher in Tideglusib-induced cells than in CHIR99021-induced cells. Conclusions Both small molecules successfully induced odontogenic differentiation of hDPSCs through Wnt/β-catenin pathway activation. Clinical relevance These findings suggest that Tideglusib and CHIR99021 can be applied clinically in pulp regeneration to improve strategies for vital pulp regeneration and to promote dentine repair.