Literature DB >> 9811576

Effects of Shh and Noggin on neural crest formation demonstrate that BMP is required in the neural tube but not ectoderm.

M A Selleck1, M I García-Castro, K B Artinger, M Bronner-Fraser.   

Abstract

To define the timing of neural crest formation, we challenged the fate of presumptive neural crest cells by grafting notochords, Sonic Hedgehog- (Shh) or Noggin-secreting cells at different stages of neurulation in chick embryos. Notochords or Shh-secreting cells are able to prevent neural crest formation at open neural plate levels, as assayed by DiI-labeling and expression of the transcription factor, Slug, suggesting that neural crest cells are not committed to their fate at this time. In contrast, the BMP signaling antagonist, Noggin, does not repress neural crest formation at the open neural plate stage, but does so if injected into the lumen of the closing neural tube. The period of Noggin sensitivity corresponds to the time when BMPs are expressed in the dorsal neural tube but are down-regulated in the non-neural ectoderm. To confirm the timing of neural crest formation, Shh or Noggin were added to neural folds at defined times in culture. Shh inhibits neural crest production at early stages (0-5 hours in culture), whereas Noggin exerts an effect on neural crest production only later (5-10 hours in culture). Our results suggest three phases of neurulation that relate to neural crest formation: (1) an initial BMP-independent phase that can be prevented by Shh-mediated signals from the notochord; (2) an intermediate BMP-dependent phase around the time of neural tube closure, when BMP-4 is expressed in the dorsal neural tube; and (3) a later pre-migratory phase which is refractory to exogenous Shh and Noggin.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9811576     DOI: 10.1242/dev.125.24.4919

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  22 in total

Review 1.  Evolution of neural crest and placodes: amphioxus as a model for the ancestral vertebrate?

Authors:  L Z Holland; N D Holland
Journal:  J Anat       Date:  2001 Jul-Aug       Impact factor: 2.610

Review 2.  Gene expression profiling within the developing neural tube.

Authors:  Richard H Finnell; Wade M Junker; Lisa Kvist Wadman; Robert M Cabrera
Journal:  Neurochem Res       Date:  2002-10       Impact factor: 3.996

3.  FGF/MAPK signaling is required in the gastrula epiblast for avian neural crest induction.

Authors:  Timothy J Stuhlmiller; Martín I García-Castro
Journal:  Development       Date:  2011-11-30       Impact factor: 6.868

Review 4.  Craniofacial birth defects: The role of neural crest cells in the etiology and pathogenesis of Treacher Collins syndrome and the potential for prevention.

Authors:  Paul A Trainor
Journal:  Am J Med Genet A       Date:  2010-08-23       Impact factor: 2.802

5.  Dynamic alterations in gene expression after Wnt-mediated induction of avian neural crest.

Authors:  Lisa A Taneyhill; Marianne Bronner-Fraser
Journal:  Mol Biol Cell       Date:  2005-08-31       Impact factor: 4.138

6.  Embryonic origin of gustatory cranial sensory neurons.

Authors:  Danielle E Harlow; Linda A Barlow
Journal:  Dev Biol       Date:  2007-08-15       Impact factor: 3.582

7.  Hand transcription factors cooperatively regulate development of the distal midline mesenchyme.

Authors:  Ana C Barbosa; Noriko Funato; Shelby Chapman; Marc D McKee; James A Richardson; Eric N Olson; Hiromi Yanagisawa
Journal:  Dev Biol       Date:  2007-08-03       Impact factor: 3.582

Review 8.  Signaling pathways and tissue interactions in neural plate border formation.

Authors:  Carolin Schille; Alexandra Schambony
Journal:  Neurogenesis (Austin)       Date:  2017-02-23

Review 9.  Cardiac outflow tract anomalies.

Authors:  Zachary Neeb; Jacquelyn D Lajiness; Esther Bolanis; Simon J Conway
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2013-02-19       Impact factor: 5.814

10.  Modeling neural crest induction, melanocyte specification, and disease-related pigmentation defects in hESCs and patient-specific iPSCs.

Authors:  Yvonne Mica; Gabsang Lee; Stuart M Chambers; Mark J Tomishima; Lorenz Studer
Journal:  Cell Rep       Date:  2013-04-11       Impact factor: 9.423

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.