𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Neural crest cells and patterning of the mammalian dentition

✍ Scribed by Martyn T. Cobourne; Thimios Mitsiadis


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
225 KB
Volume
306B
Category
Article
ISSN
1552-5007

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The mammalian dentition is composed of serial groups of teeth, each with a distinctive crown and root morphology, highly adapted to its particular masticatory function. In the embryo, generation of individual teeth within the jaws relies upon interactions between ectoderm of the first branchial arch and the neural crest‐derived ectomesenchymal cells that migrate into this region from their site of origin along the neural axis. Classic tissue recombination experiments have provided evidence of an essential role of the ectoderm in initiating tooth development; however, the underlying ectomesenchyme rapidly acquires dominance in establishing shape. A key question is how these cells acquire this positional information. One theory suggests that ectomesenchymal cells are pre‐patterned with respect to shape generation. Alternatively, this cell population acquires positional information within the first branchial arch itself, following migration. Recent molecular evidence suggests a high degree of plasticity within these ectomesenchymal cells. In particular, signalling molecules within the ectoderm exert a time‐dependent influence upon the ectomesenchyme by establishing specific domains of homeobox gene expression. Initially, these ectomesenchymal cells are plastic and able to respond to signalling from the ectoderm, however, this plasticity is rapidly lost and pattern information becomes fixed. Therefore, in the first branchial arch, local regulation between the ectoderm and neural crest‐derived ectomesenchyme is crucial in establishing the appropriate tooth shape in the correct region of the jaw. J. Exp. Zool. (Mol. Dev. Evol.) 306B, 2006. Β© 2005 Wiley‐Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Induction and patterning of the neural c
✍ LaBonne, Carole ;Bronner-Fraser, Marianne πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 348 KB πŸ‘ 2 views

The neural crest is a multipotent precursor population which ultimately generates much of the peripheral nervous system, epidermal pigment cells, and a variety of mesectodermal derivatives. Individual multipotent neural crest cells are capable of some self-renewing divisions, and based upon this cri

Molecular mechanisms of segmental patter
✍ David G. Wilkinson πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 936 KB

Recent work has shown that segmentation underlies the patterning of the vertebrate hindbrain and its neural crest derivatives. Several genes have been identified with segment-restricted expression, and evidence is now emerging regarding their function and regulatory relationships. The expression pat

Distribution patterns of neural-crest-de
✍ Faas, Laura ;Rovasio, Roberto A. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 413 KB πŸ‘ 2 views

Background: In vertebrate embryos, migration of trunk neural crest cells (NCC) proceeds mainly in two streams: a dorsoventral path between the neural tube and somites, and a dorsolateral one between somites and ectoderm. This last pathway is taken by melanocyte precursor cells (MPC) homing the skin,

The proliferating field of neural crest
✍ Mariana Delfino-MachΓ­n; Thomas R. Chipperfield; Frederico S.L.M. Rodrigues; Robe πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 508 KB
Chemotactic migration of mesencephalic n
✍ Yukihiko Kubota; Kazuo Ito πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 695 KB

We examined the roles of fibroblast growth factor (FGF)-2 and FGF-8 in the migration of mesencephalic mouse neural crest cells. Our in vitro migration assay has shown that FGF-2 (basic FGF) and FGF-8 have chemotactic activity for these cells. Chemotaxis was inhibited by anti-FGF-2 and anti-FGF-8 neu