𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Epithelial-specific requirement of FGFR2 signaling during tooth and palate development

✍ Scribed by Ryoichi Hosokawa; Xuemei Deng; Kazunori Takamori; Xun Xu; Mark Urata; Pablo Bringas Jr; Yang Chai


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
605 KB
Volume
312B
Category
Article
ISSN
1552-5007

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Reciprocal interactions between epithelium and mesenchyme are crucial for embryonic development. Fibroblast growth factors (FGFs) are a growth factor family that play an important role in epithelial–mesenchymal tissue interaction. We have generated epithelial‐specific conditional knockout mice targeting Fibroblast growth factor receptor 2 (Fgfr2) to investigate the function of FGF signaling during craniofacial development. K14‐Cre;Fgfr2^fl/fl^ mice have skin defects, retarded tooth formation, and cleft palate. During the formation of the tooth primordium and palatal processes, cell proliferation in the epithelial cells of K14‐Cre;Fgfr2^fl/fl^ mice is reduced. Thus, FGF signaling via FGFR2 in the epithelium is crucial for cell proliferation activity during tooth and palate development. J. Exp. Zool. (Mol. Dev. Evol.) 312B:343–350, 2009. © 2009 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Concepts of epithelial-mesenchymal inter
✍ Harold C. Slavkin; Malcolm L. Snead; Margarita Zeichner-David; Tina F. Jaskoll; 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 577 KB

One of the major problems in developmental biology concerns how differential gene activity is regionally controlled. One approach to this problem is the use of mesenchyme specification of epithelial-specific gene expression, such as, during tooth morphogenesis or lung morphogenesis. In the example o

Specific signaling cascades involved in
✍ Marie-Pier Tétreault; Pierre Chailler; Jean-François Beaulieu; Nathalie Rivard; 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 357 KB

## Abstract Mechanisms that specifically modulate cell spreading and/or cell migration following epithelial wounding are poorly understood. Using micro‐wounded human gastric epithelial monolayers, we show herein that EGF and TGFα maximally increase spreading of epithelial sheets under a cell prolif