PLoS ONE · 2007 · 132 citations · 44 references
Life SciencesCell BiologyDevelopmental BiologyCraniofacial DevelopmentEmbryogenesisMorphogenesisCranial Neural Crest SpecificationCraniofacial MorphogenesisEpithelial-mesenchymal InteractionsEpithelial-to-mesenchymal TransitionNeural Crest DevelopmentNeural DevelopmentCephalic Mesenchyme DevelopmentCephalic Neural Crest MigrationCephalic StructuresCranial Neural Crest CellsNeural Crest Cell BiologyNeural Crest Epithelial-to-mesenchymal TransitionNeural Crest MorphogenesisTranscription Factor Cooperation
Neural crest cells (NCC) have the particularity to invade the environment where they differentiate after separation from the neuroepithelium. This process, called delamination, is strikingly different between cranial and trunk NCCs. If signalings controlling slow trunk delamination start being deciphered, mechanisms leading to massive and rapid cranial outflow are poorly documented. Here, we show that the chick cranial NCCs delamination is the result of two events: a substantial cell mobilization and an epithelium to mesenchyme transition (EMT). We demonstrate that ets-1, a transcription factor specifically expressed in cranial NCCs, is responsible for the former event by recruiting massively cranial premigratory NCCs independently of the S-phase of the cell cycle and by leading the gathered cells to straddle the basal lamina. However, it does not promote the EMT process alone but can cooperate with snail-2 (previously called slug) to this event. Altogether, these data lead us to propose that ets-1 plays a pivotal role in conferring specific cephalic characteristics on NCC delamination.
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Opposing effects of Ets and Id proteins on p16INK4a expression during cellular senescence
Naoko Ohtani, Zoë Zebedee, Thomas J. G. Huot et al. · Nature · 2001 · 641 citations