共 47 条
Glycogen synthase kinase-3β inhibitor promotes the migration and osteogenic differentiation of rat dental pulp stem cells via the β-catenin/PI3K/Akt signaling pathway
被引:19
作者:

Xie, Huilan
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机构:
Fujian Prov Hosp, Dept Stomatol, Fuzhou, Fujian, Peoples R China Fujian Prov Hosp, Dept Stomatol, Fuzhou, Fujian, Peoples R China

Lin, Yi
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h-index: 0
机构:
Fujian Prov Hosp, Dept Stomatol, Fuzhou, Fujian, Peoples R China Fujian Prov Hosp, Dept Stomatol, Fuzhou, Fujian, Peoples R China

Fang, Fang
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h-index: 0
机构:
Fujian Prov Hosp, Dept Stomatol, Fuzhou, Fujian, Peoples R China Fujian Prov Hosp, Dept Stomatol, Fuzhou, Fujian, Peoples R China
机构:
[1] Fujian Prov Hosp, Dept Stomatol, Fuzhou, Fujian, Peoples R China
关键词:
Glycogen synthase kinase-3 beta inhibitor;
Dental pulp stem cells;
Migration;
Osteogenic differentiation;
PI3K;
BONE REGENERATION;
PROLIFERATION;
GSK-3-BETA;
SURVIVAL;
D O I:
10.1016/j.jds.2021.09.035
中图分类号:
R78 [口腔科学];
学科分类号:
1003 ;
摘要:
Background/purpose: Glycogen synthase kinase-3b ( GSK3b) inhibitor enhances bone formation, while dental pulp stem cells (DPSC) are potentially used to repair bone defects. The present study aimed to investigate the effect of AR-A014418 (AR, a specific glycogen synthase kinase-3b inhibitor) on the migration and osteogenic differentiation of rat-derived dental pulp stem cells (rDPSCs), and further explore the underlying mechanism. Materials and methods: rDPSCs were isolated from rats, and then cultured with different concentrations of AR with or without LY294002 (a PI3K inhibitor). Then, cell viability, migration, osteogenic differentiation, and the involvement of PI3K pathway were detected by CCK-8 assay, Transwell assay, Alizarin Red S Staining, Alkaline phosphatase (ALP) assay, Western blot, and RT-PCR, respectively. Results: Our present study demonstrated that AR of various concentrations (1 mM, 2.5 mM, and 5 mM) not only promoted the rDPSC proliferation and migration, but also increased calcium deposition, the activity of alkaline phosphatase (ALP), and levels of osteogenic markers (RUNX2, OPN, OCN, and OSX) in rDPSCs. It was also found that the administration of AR resulted in an increase in the expression level of p- GSK3b (Ser), beta-catenin, p-PI3K, and p-Akt, and a reduction in p-GSK3b (Tyr216). Furthermore, PI3K inhibitor LY294002 abrogated the enhanced cell migration and osteogenic differentiation of rDPSCs induced by AR. Conclusion: Our results provide evidence that AR significantly promotes migration and osteogenic differentiation of rDPSCs by activating beta-catenin/PI3K/Akt signaling pathway. (C) 2021 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V.
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页码:802 / 810
页数:9
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