| First Author | Javali A | Year | 2020 |
| Journal | Dev Dyn | Volume | 249 |
| Issue | 11 | Pages | 1347-1364 |
| PubMed ID | 32427396 | Mgi Jnum | J:297161 |
| Mgi Id | MGI:6471833 | Doi | 10.1002/dvdy.208 |
| Citation | Javali A, et al. (2020) Modulation of beta-catenin levels regulates cranial neural crest patterning and dispersal into first pharyngeal arch. Dev Dyn |
| abstractText | BACKGROUND: Vertebrate cranial neural crest cells (CNCCs) are multipotent, proximal to the source CNCC form the cranial ganglia. Distally, in the pharyngeal arches, they give rise to the craniofacial skeleton and connective tissues. Fate choices are made as CNCC pattern into distinct destination compartments. In spite of this importance, the mechanism patterning CNCC is poorly defined. RESULTS: Here, we report that a novel beta-catenin-dependent regulation of N-Cadherin levels may drive CNCC patterning. In mouse embryos, at the first pharyngeal arch axial level, membrane beta-catenin levels correlate with the extent of N-cadherin-mediated adhesion and thus suggest the presence of collective and dispersed states of CNCC. Using in vitro human neural crest model and chemical modulators of beta-catenin levels, we show a requirement for down-modulating beta-catenin for regulating N-cadherin levels and cell-cell adhesion. Similarly, in beta-catenin gain-of-function mutant mouse embryos, CNCC fail to lower N-cadherin levels. This indicates a failure to reduce cell-cell adhesion, which may underlie the failure of mutant CNCC to populate first pharyngeal arch. CONCLUSION: We suggest that beta-catenin-mediated regulation of CNCC adhesion, a previously underappreciated mechanism, underlies the patterning of CNCC into fate-specific compartments. |
