In mice, the incisors grow throughout the animal's life, and this continuous renewal is driven by dental epithelial and mesenchymal stem cells. is a principal marker of the epithelial stem cells that reside in the mouse incisor stem cell niche, called the labial cervical loop, but relatively little is known about the role of the stem cell population. In this study, we show that conditional deletion of in the embryonic incisor epithelium leads to growth defects and impairment of ameloblast lineage commitment. Deletion of specifically in cells during incisor renewal revealed cellular plasticity that leads to the relatively rapid restoration of a-expressing cell population. Furthermore, we show that -expressing cells are a subpopulation of dental cells that also arise from cells during tooth formation. Finally, we show that the embryonic and adult populations are regulated by distinct signalling pathways, which is reflected in their distinct transcriptomic signatures. Together, our findings demonstrate that a stem cell population can be regenerated from cells, reinforcing its importance for incisor homeostasis.