The identification of critical time windows of postnatal root elongation in response to Wnt/β-catenin signaling

Objectives: In this study, we attempted to define the precise window of time for molar root elongation using a gain-of-function mutation of beta-catenin model. Materials and Methods: Both the control and constitutively activated beta-catenin (CA-beta-cat) mice received a one-time tamoxifen administration (for activation of beta-catenin at newborn, postnatal day 3, or 5, or 7, or 9) and were harvested at the same stage of P21. Multiple approaches were used to define the window of time of postnatal tooth root formation. Results: In the early activation groups (tamoxifen induction at newborn, or P3 or P5), there was a lack of molar root elongation in the CA-beta-cat mice. When induced at P7, the root length was slightly reduced at P21. However, the root length was essentially the same as that in the control when beta-cat activated at P9. This study indicates that root elongation occurs in a narrow time of window, which is highly sensitive to a change of beta-catenin levels. Molecular studies showed a drastic decrease in the levels of nuclear factor I-C (NFIC) and osterix (OSX), plus sharp reductions of odontoblast differentiation markers, including Nestin, dentin sialoprotein (DSP), and dentin matrix protein 1 (DMP1) at both mRNA and protein levels. Conclusions: Murine molar root elongation is precisely regulated by the Wnt/beta-catenin signaling within a narrow window of time (newborn to day 5).

Automated summary

This study demonstrates that murine molar root elongation is precisely regulated by Wnt/beta-catenin signaling within a narrow window of time, from newborn to the 5th day. Activation of beta-catenin at different time points affects the extent of root elongation, indicating a high sensitivity of root elongation to changes in beta-catenin levels.