Induction of human stem cells into ameloblasts by reaggregation strategy

• Published in: Stem cell research & therapy Vol. 15; no. 1; pp. 332 - 10
• Main Authors: Lin, Chensheng, Liu, Shiyu, Huang, Minjun, Zhang, Yanding, Hu, Xuefeng
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 27.09.2024; BioMed Central; BMC
• Subjects: Ameloblast; Ameloblasts - cytology; Ameloblasts - metabolism; Analysis; Animals; Cell Aggregation; Cell Differentiation; Cells, Cultured; Humans; Induced pluripotent stem cell; Induced Pluripotent Stem Cells - cytology; Induced Pluripotent Stem Cells - metabolism; Keratinocyte; Keratinocytes - cytology; Keratinocytes - metabolism; Mesenchymal Stem Cells - cytology; Mesenchymal Stem Cells - metabolism; Mice; Reaggregate; Stem cells; Tooth Germ - cytology; Tooth Germ - metabolism; Tooth regeneration; Induced pluripotent stem cell; Keratinocyte; Tooth regeneration; Ameloblast; Reaggregate
• ISSN: 1757-6512; 1757-6512
• DOI: 10.1186/s13287-024-03948-1

Human epithelium-derived stem cells and induced pluripotent stem cells (hiPSCs) possess the capability to support tooth formation and differentiate into functional enamel-secreting ameloblasts, making them promising epithelial-component substitutes for future human tooth regeneration. However, current tissue recombination approaches are not only technically challenging, requiring precise induction procedures and sophisticated microsurgery, but also exhibit low success rates in achieving tooth formation and ameloblastic differentiation. Suspended human keratinocyte stem cells (hKSCs) or cells from three hiPSC lines were directly mixed with dissociated embryonic mouse dental mesenchymal cells (mDMCs) that possess odontogenic potential in different proportions and reaggregated them to construct bioengineered tooth germs. The success rates of tooth formation and ameloblastic differentiation were confirmed after subrenal culture. The sorting capability, sequential development, and ameloblastic differentiation of stem cells were examined via GFP tracing, RT-PCR, and histological analysis, respectively. Our reaggregation approach achieved an impressive success rate of more than 90% in tooth formation and 100% in ameloblastic differentiation when the chimeric tooth germs contained 1%~10% hKSCs or 5% hiPSCs. In addition, we observed that hiPSCs, upon exposure to mDMCs, initially transformed into epidermal cells, as indicated by KRT14 and CD29 expression, before progressing into dental epithelial cells, as indicated by SP6 and SHH expression. We also found that epithelial-derived hiPSCs, when reaggregated with mDMCs, were more favorable for tooth formation than their mesenchymal-derived counterparts. This study establishes a simplified yet highly effective cell-cell reaggregation strategy for inducing stem cells to support tooth formation and differentiate into functional ameloblasts, paving the way for novel approaches for the development of stem cell-based tooth organoids and bioengineered tooth germs in vitro.