article · 01/05/2015
Cranial placodes: Models for exploring the multi-facets of cell adhesion in epithelial rearrangement, collective migration and neuronal movements
Résumé
Key to morphogenesis is the orchestration of cell movements in the embryo, which requires fine-tuned adhesive interactions between cells and their close environment. The neural crest paradigm has provided important insights into how adhesion dynamics control epithelium-to-mesenchyme transition and mesenchymal cell migration. Much less is known about cranial placodes, patches of ectodermal cells that generate essential parts of vertebrate sensory organs and ganglia. In this review, we summarise the known functions of adhesion molecules in cranial placode morphogenesis, and discuss potential novel implications of adhesive interactions in this crucial developmental process. The great repertoire of placodal cell behaviours offers new avenues for exploring the multiple roles of adhesion complexes in epithelial remodelling, collective migration and neuronal movements. (C) 2014 Elsevier Inc. All rights reserved.
Citer cet article
Breau, M.-A., & Schneider-Maunoury, S. (2015). Cranial placodes: Models for exploring the multi-facets of cell adhesion in epithelial rearrangement, collective migration and neuronal movements. Dev. Biol., 401(1, SI). https://doi.org/10.1016/j.ydbio.2014.12.012@article{Breau2015_265,
author = {Breau, Marie Anne and Schneider-Maunoury, Sylvie},
year = {2015},
month = {5},
title = {Cranial placodes: Models for exploring the multi-facets of cell adhesion in epithelial rearrangement, collective migration and neuronal movements},
journal = {Dev. Biol.},
publisher = {ACADEMIC PRESS INC ELSEVIER SCIENCE},
volume = {401},
number = {1, SI},
address = {525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA},
abstract = {Key to morphogenesis is the orchestration of cell movements in the embryo, which requires fine-tuned adhesive interactions between cells and their close environment. The neural crest paradigm has provided important insights into how adhesion dynamics control epithelium-to-mesenchyme transition and mesenchymal cell migration. Much less is known about cranial placodes, patches of ectodermal cells that generate essential parts of vertebrate sensory organs and ganglia. In this review, we summarise the known functions of adhesion molecules in cranial placode morphogenesis, and discuss potential novel implications of adhesive interactions in this crucial developmental process. The great repertoire of placodal cell behaviours offers new avenues for exploring the multiple roles of adhesion complexes in epithelial remodelling, collective migration and neuronal movements. (C) 2014 Elsevier Inc. All rights reserved.},
url = {http://www.dx.doi.org/10.1016/j.ydbio.2014.12.012},
doi = {10.1016/j.ydbio.2014.12.012},
issn = {0012-1606},
}TY - JOUR
AU - Breau, Marie Anne
AU - Schneider-Maunoury, Sylvie
PY - 2015
DA - 2015/05/01
TI - Cranial placodes: Models for exploring the multi-facets of cell adhesion in epithelial rearrangement, collective migration and neuronal movements
JO - Dev. Biol.
VL - 401
IS - 1, SI
PB - ACADEMIC PRESS INC ELSEVIER SCIENCE
SN - 0012-1606
AB - Key to morphogenesis is the orchestration of cell movements in the embryo, which requires fine-tuned adhesive interactions between cells and their close environment. The neural crest paradigm has provided important insights into how adhesion dynamics control epithelium-to-mesenchyme transition and mesenchymal cell migration. Much less is known about cranial placodes, patches of ectodermal cells that generate essential parts of vertebrate sensory organs and ganglia. In this review, we summarise the known functions of adhesion molecules in cranial placode morphogenesis, and discuss potential novel implications of adhesive interactions in this crucial developmental process. The great repertoire of placodal cell behaviours offers new avenues for exploring the multiple roles of adhesion complexes in epithelial remodelling, collective migration and neuronal movements. (C) 2014 Elsevier Inc. All rights reserved.
DO - 10.1016/j.ydbio.2014.12.012
UR - http://www.dx.doi.org/10.1016/j.ydbio.2014.12.012
ER -