ALK5 is essential for tooth germ differentiation during tooth development

• Published in: Biotechnic & histochemistry Vol. 94; no. 7; pp. 481 - 490
• Main Authors: Guo, W., Fan, Z., Wang, S., Du, J.
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 03.10.2019
• Subjects: ALK5; Animals; Cell Differentiation - physiology; Cell Proliferation - physiology; dentinogenes; Female; Male; Mesenchymal Stem Cells - cytology; Mice, Inbred ICR; Odontogenesis - physiology; osteogenesis; Receptor, Transforming Growth Factor-beta Type I - metabolism; Signal Transduction - physiology; Stem Cells - cytology; TGFβ3; Tooth - cytology; Tooth Germ - cytology; Tooth Germ - metabolism; tooth germ mesenchymal cells; Wnt Proteins - metabolism; ALK5; osteogenesis; TGFβ3; dentinogenes; tooth germ mesenchymal cells
• ISSN: 1052-0295; 1473-7760; 1473-7760
• DOI: 10.1080/10520295.2018.1552018

The TGFβ superfamily of proteins participates in tooth development. TGFβ1 and TGFβ3 regulate odontoblast differentiation and dentin extracellular matrix synthesis. Although the expression of TGFβ family member ligands is well-characterized during mammalian tooth development, less is known about the TGFβ receptor, which is a heteromeric complex consisting of a type I and type II receptors. The molecular mechanism of ALK5 (TGFβR1) in the dental mesenchyme is not clear. We investigated the role of ALK5 in tooth germ mesenchymal cells (TGMCs) from the lower first molar tooth germs of day 15.5 embryonic mice. Human recombinant TGFβ3 protein or an ALK5 inhibitor (SD208) was added to the cells. Cell proliferation was inhibited by SD208 and promoted by TGFβ3. We found that SD208 inhibited TGMCs osteogenesis and dentinogenesis. Both canonical and noncanonical TGFβ signaling pathways participated in the process. TAK1, P-TAK1, p38 and P-p38 showed greater expression and SMAD4 showed less expression when ALK5 was inhibited. Our findings contribute to understanding the role of TGFβ signaling for the differentiation of mesenchymal stem cells derived from dental germ and suggest possible targets for optimizing the use of stem cells of dental origin for tissue regeneration.