Literature DB >> 10585567

Expression of FGFR1, FGFR2 and FGFR3 during early neural development in the chick embryo.

J Walshe1, I Mason.   

Abstract

Studies involving chick embryos have implicated FGFs in neural induction and patterning as well as in other developmental events. Detailed analyses of FGF receptor expression at early stages of neural development have not been reported for the chick embryo and are incomplete for other vertebrate classes. Here we show the expression patterns of three FGF receptors, (FGFR1, FGFR2 and FGFR3) in embryonic stages between gastrulation and limb bud formation, focussing particularly on neural tissues. Between neural induction and neurulation, all three receptors are expressed in the neural plate albeit with distinct and overlapping distributions. During early neuromere formation FGFR1 transcripts are present throughout the neural tube, while transcripts for FGFR2 and FGFR3 become restricted to regions of the diencephalon and spinal cord. A little later, FGFR2 and FGFR3 are additionally expressed in the anterior midbrain and within the hindbrain. During later neuromere development, FGFR1 transcripts become localised to the telencephalon, anterior dorsal diencephalon and throughout the midbrain and hindbrain, whereas FGFR2 mRNA is restricted to dorsal telencephalon, dorsoanterior midbrain and hindbrain. FGFR3 is also expressed in anterior midbrain and hindbrain during this developmental period, and is additionally expressed in the posterior telencephalon, in the pretectum, and at the zona limitans intrathalamica. The observed expression patterns of all three receptors within the hindbrain, including rhombomere boundaries, are complex and dynamic. Expression patterns within the somites, eye, head mesenchyme, branchial arches, limb buds, nephric kidney and pharynx are also described.

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Year:  2000        PMID: 10585567     DOI: 10.1016/s0925-4773(99)00225-7

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  32 in total

1.  Expansion, folding, and abnormal lamination of the chick optic tectum after intraventricular injections of FGF2.

Authors:  Luke D McGowan; Roula A Alaama; Amanda C Freise; Johnny C Huang; Christine J Charvet; Georg F Striedter
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-20       Impact factor: 11.205

Review 2.  An essential role for FGF receptor signaling in lens development.

Authors:  Michael L Robinson
Journal:  Semin Cell Dev Biol       Date:  2006-10-27       Impact factor: 7.727

Review 3.  Primary cultures of embryonic chick lens cells as a model system to study lens gap junctions and fiber cell differentiation.

Authors:  Linda S Musil
Journal:  J Membr Biol       Date:  2012-07-15       Impact factor: 1.843

4.  FGFR1 is independently required in both developing mid- and hindbrain for sustained response to isthmic signals.

Authors:  Ras Trokovic; Nina Trokovic; Sanna Hernesniemi; Ulla Pirvola; Daniela M Vogt Weisenhorn; Janet Rossant; Andrew P McMahon; Wolfgang Wurst; Juha Partanen
Journal:  EMBO J       Date:  2003-04-15       Impact factor: 11.598

5.  Prolyl isomerase Pin1-mediated conformational change and subnuclear focal accumulation of Runx2 are crucial for fibroblast growth factor 2 (FGF2)-induced osteoblast differentiation.

Authors:  Won-Joon Yoon; Young-Dan Cho; Woo-Jin Kim; Han-Sol Bae; Rabia Islam; Kyung-Mi Woo; Jeong-Hwa Baek; Suk-Chul Bae; Hyun-Mo Ryoo
Journal:  J Biol Chem       Date:  2014-02-07       Impact factor: 5.157

6.  Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10.

Authors:  E Rampersaud; A G Bassuk; D S Enterline; T M George; D G Siegel; E C Melvin; J Aben; J Allen; A Aylsworth; T Brei; J Bodurtha; C Buran; L E Floyd; P Hammock; B Iskandar; J Ito; J A Kessler; N Lasarsky; P Mack; J Mackey; D McLone; E Meeropol; L Mehltretter; L E Mitchell; W J Oakes; J S Nye; C Powell; K Sawin; R Stevenson; M Walker; S G West; G Worley; J R Gilbert; M C Speer
Journal:  J Med Genet       Date:  2005-04-14       Impact factor: 6.318

7.  Modeling gastrulation in the chick embryo: formation of the primitive streak.

Authors:  Bakhtier Vasiev; Ariel Balter; Mark Chaplain; James A Glazier; Cornelis J Weijer
Journal:  PLoS One       Date:  2010-05-11       Impact factor: 3.240

8.  Cubilin, a high affinity receptor for fibroblast growth factor 8, is required for cell survival in the developing vertebrate head.

Authors:  Olivier Cases; Aitana Perea-Gomez; Diego P Aguiar; Anders Nykjaer; Sabine Amsellem; Jacqueline Chandellier; Muriel Umbhauer; Silvia Cereghini; Mette Madsen; Jérôme Collignon; Pierre Verroust; Jean-François Riou; Sophie E Creuzet; Renata Kozyraki
Journal:  J Biol Chem       Date:  2013-04-16       Impact factor: 5.157

Review 9.  Signals and switches in Mammalian neural crest cell differentiation.

Authors:  Shachi Bhatt; Raul Diaz; Paul A Trainor
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-02-01       Impact factor: 10.005

10.  Zebrafish fgfr1 is a member of the fgf8 synexpression group and is required for fgf8 signalling at the midbrain-hindbrain boundary.

Authors:  Steffen Scholpp; Casper Groth; Claudia Lohs; Michael Lardelli; Michael Brand
Journal:  Dev Genes Evol       Date:  2004-05-25       Impact factor: 0.900

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