Literature DB >> 16966604

The cephalic neural crest exerts a critical effect on forebrain and midbrain development.

Sophie E Creuzet1, Salvador Martinez, Nicole M Le Douarin.   

Abstract

Encephalisation is the most important characteristic in the evolutionary transition leading from protochordates to vertebrates. This event has coincided with the emergence of a transient and pluripotent structure, the neural crest (NC), which is absent in protochordates. In vertebrates, NC provides the rostral cephalic vesicles with skeletal protection and functional vascularization. The surgical extirpation of the cephalic NC, which is responsible for building up the craniofacial skeleton, results in the absence of facial skeleton together with severe defects of preotic brain development, leading to exencephaly. Here, we have analyzed the role of the NC in forebrain and midbrain development. We show that (i) NC cells (NCC) control Fgf8 expression in the anterior neural ridge, which is considered the prosencephalic organizer; (ii) the cephalic NCC are necessary for the closure of the neural tube; and (iii) NCC contribute to the proper patterning of genes that are expressed in the prosencephalic and mesencephalic alar plate. Along with the development of the roof plate, NCC also concur to the patterning of the pallial and subpallial structures. We show that the NC-dependent production of FGF8 in anterior neural ridge is able to restrict Shh expression to the ventral prosencephalon. All together, these findings support the notion that the cephalic NC controls the formation of craniofacial structures and the development of preotic brain.

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Year:  2006        PMID: 16966604      PMCID: PMC1599907          DOI: 10.1073/pnas.0605899103

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  33 in total

1.  A series of normal stages in the development of the chick embryo.

Authors:  V HAMBURGER; H L HAMILTON
Journal:  J Morphol       Date:  1951-01       Impact factor: 1.804

2.  Pallial and subpallial derivatives in the embryonic chick and mouse telencephalon, traced by the expression of the genes Dlx-2, Emx-1, Nkx-2.1, Pax-6, and Tbr-1.

Authors:  L Puelles; E Kuwana; E Puelles; A Bulfone; K Shimamura; J Keleher; S Smiga; J L Rubenstein
Journal:  J Comp Neurol       Date:  2000-08-28       Impact factor: 3.215

3.  The midbrain-hindbrain phenotype of Wnt-1-/Wnt-1- mice results from stepwise deletion of engrailed-expressing cells by 9.5 days postcoitum.

Authors:  A P McMahon; A L Joyner; A Bradley; J A McMahon
Journal:  Cell       Date:  1992-05-15       Impact factor: 41.582

4.  Zebrafish aussicht mutant embryos exhibit widespread overexpression of ace (fgf8) and coincident defects in CNS development.

Authors:  C P Heisenberg; C Brennan; S W Wilson
Journal:  Development       Date:  1999-05       Impact factor: 6.868

5.  Homeotic transformation of branchial arch identity after Hoxa2 overexpression.

Authors:  G A Grammatopoulos; E Bell; L Toole; A Lumsden; A S Tucker
Journal:  Development       Date:  2000-12       Impact factor: 6.868

6.  A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo.

Authors:  T P Yamaguchi; A Bradley; A P McMahon; S Jones
Journal:  Development       Date:  1999-03       Impact factor: 6.868

7.  Determination of the identity of the derivatives of the cephalic neural crest: incompatibility between Hox gene expression and lower jaw development.

Authors:  G Couly; A Grapin-Botton; P Coltey; B Ruhin; N M Le Douarin
Journal:  Development       Date:  1998-09       Impact factor: 6.868

8.  Expression of the Emx-1 and Dlx-1 homeobox genes define three molecularly distinct domains in the telencephalon of mouse, chick, turtle and frog embryos: implications for the evolution of telencephalic subdivisions in amniotes.

Authors:  A S Fernandez; C Pieau; J Repérant; E Boncinelli; M Wassef
Journal:  Development       Date:  1998-06       Impact factor: 6.868

9.  Inductive interactions direct early regionalization of the mouse forebrain.

Authors:  K Shimamura; J L Rubenstein
Journal:  Development       Date:  1997-07       Impact factor: 6.868

10.  The regeneration of the cephalic neural crest, a problem revisited: the regenerating cells originate from the contralateral or from the anterior and posterior neural fold.

Authors:  G Couly; A Grapin-Botton; P Coltey; N M Le Douarin
Journal:  Development       Date:  1996-11       Impact factor: 6.868

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  25 in total

Review 1.  Cranial neural crest cells on the move: their roles in craniofacial development.

Authors:  Dwight R Cordero; Samantha Brugmann; Yvonne Chu; Ruchi Bajpai; Maryam Jame; Jill A Helms
Journal:  Am J Med Genet A       Date:  2010-12-10       Impact factor: 2.802

Review 2.  Cell lineages and early patterns of embryonic CNS vascularization.

Authors:  Haymo Kurz
Journal:  Cell Adh Migr       Date:  2009-04-16       Impact factor: 3.405

Review 3.  Evolution of vertebrates as viewed from the crest.

Authors:  Stephen A Green; Marcos Simoes-Costa; Marianne E Bronner
Journal:  Nature       Date:  2015-04-23       Impact factor: 49.962

4.  Regulation of pre-otic brain development by the cephalic neural crest.

Authors:  Sophie E Creuzet
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-31       Impact factor: 11.205

Review 5.  Craniofacial malformations and their association with brain development: the importance of a multidisciplinary approach for treatment.

Authors:  Asher Ornoy
Journal:  Odontology       Date:  2019-06-06       Impact factor: 2.634

6.  Neural crest cells utilize primary cilia to regulate ventral forebrain morphogenesis via Hedgehog-dependent regulation of oriented cell division.

Authors:  Elizabeth N Schock; Samantha A Brugmann
Journal:  Dev Biol       Date:  2017-09-21       Impact factor: 3.582

Review 7.  Development and evolution of the neural crest: an overview.

Authors:  Marianne E Bronner; Nicole M LeDouarin
Journal:  Dev Biol       Date:  2012-01-02       Impact factor: 3.582

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

9.  SP8 regulates signaling centers during craniofacial development.

Authors:  Abigail D Kasberg; Eric W Brunskill; S Steven Potter
Journal:  Dev Biol       Date:  2013-07-18       Impact factor: 3.582

10.  Olfactory anomalies in CHARGE syndrome: imaging findings of a potential major diagnostic criterion.

Authors:  J Blustajn; C F E Kirsch; A Panigrahy; I Netchine
Journal:  AJNR Am J Neuroradiol       Date:  2008-04-16       Impact factor: 3.825

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