Literature DB >> 19235875

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

Ryoichi Hosokawa1, Xuemei Deng, Kazunori Takamori, Xun Xu, Mark Urata, Pablo Bringas, Yang Chai.   

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. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19235875      PMCID: PMC2896559          DOI: 10.1002/jez.b.21274

Source DB:  PubMed          Journal:  J Exp Zool B Mol Dev Evol        ISSN: 1552-5007            Impact factor:   2.656


  39 in total

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Authors:  Yang Chai; Robert E Maxson
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Journal:  EMBO J       Date:  2007-02-15       Impact factor: 11.598

5.  Ectodermal Smad4 and p38 MAPK are functionally redundant in mediating TGF-beta/BMP signaling during tooth and palate development.

Authors:  Xun Xu; Jun Han; Yoshihiro Ito; Pablo Bringas; Chuxia Deng; Yang Chai
Journal:  Dev Cell       Date:  2008-08       Impact factor: 12.270

6.  Smad4 is required to regulate the fate of cranial neural crest cells.

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7.  PITX2 and beta-catenin interactions regulate Lef-1 isoform expression.

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8.  An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis.

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9.  Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis.

Authors:  Y Chai; X Jiang; Y Ito; P Bringas; J Han; D H Rowitch; P Soriano; A P McMahon; H M Sucov
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10.  Temporal and spatial expression of Pax9 and Sonic hedgehog during development of normal mouse palates and cleft palates in TGF-beta3 null embryos.

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  31 in total

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2.  Risk of breast cancer in families with cleft lip and palate.

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Review 3.  Palatogenesis: morphogenetic and molecular mechanisms of secondary palate development.

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Review 4.  Closing the Gap: Mouse Models to Study Adhesion in Secondary Palatogenesis.

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5.  Expression of fibroblast growth factors (Fgfs) in murine tooth development.

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7.  Mesenchymal fibroblast growth factor receptor signaling regulates palatal shelf elevation during secondary palate formation.

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Journal:  Dev Dyn       Date:  2015-08-24       Impact factor: 3.780

8.  Type 1 fibroblast growth factor receptor in cranial neural crest cell-derived mesenchyme is required for palatogenesis.

Authors:  Cong Wang; Julia Yu Fong Chang; Chaofeng Yang; Yanqing Huang; Junchen Liu; Pan You; Wallace L McKeehan; Fen Wang; Xiaokun Li
Journal:  J Biol Chem       Date:  2013-06-10       Impact factor: 5.157

Review 9.  From Bench to Bedside and Back: Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models.

Authors:  Alice F Goodwin; Rebecca Kim; Jeffrey O Bush; Ophir D Klein
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10.  Expression Analysis of FGF/FGFR and FOX Family Proteins in Mucosal Tissue Obtained from Orofacial Cleft-Affected Children.

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