Literature DB >> 7768190

Origins of the avian neural crest: the role of neural plate-epidermal interactions.

M A Selleck1, M Bronner-Fraser.   

Abstract

We have investigated the lineage and tissue interactions that result in avian neural crest cell formation from the ectoderm. Presumptive neural plate was grafted adjacent to non-neural ectoderm in whole embryo culture to examine the role of tissue interactions in ontogeny of the neural crest. Our results show that juxtaposition of non-neural ectoderm and presumptive neural plate induces the formation of neural crest cells. Quail/chick recombinations demonstrate that both the prospective neural plate and the prospective epidermis can contribute to the neural crest. When similar neural plate/epidermal confrontations are performed in tissue culture to look at the formation of neural crest derivatives, juxtaposition of epidermis with either early (stages 4-5) or later (stages 6-10) neural plate results in the generation of both melanocytes and sympathoadrenal cells. Interestingly, neural plates isolated from early stages form no neural crest cells, whereas those isolated later give rise to melanocytes but not crest-derived sympathoadrenal cells. Single cell lineage analysis was performed to determine the time at which the neural crest lineage diverges from the epidermal lineage and to elucidate the timing of neural plate/epidermis interactions during normal development. Our results from stage 8 to 10+ embryos show that the neural plate/neural crest lineage segregates from the epidermis around the time of neural tube closure, suggesting that neural induction is still underway at open neural plate stages.

Entities:  

Mesh:

Year:  1995        PMID: 7768190     DOI: 10.1242/dev.121.2.525

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


  75 in total

1.  Dlx proteins position the neural plate border and determine adjacent cell fates.

Authors:  Juliana M Woda; Julie Pastagia; Mark Mercola; Kristin Bruk Artinger
Journal:  Development       Date:  2003-01       Impact factor: 6.868

2.  Neural crest-specific loss of Prkar1a causes perinatal lethality resulting from defects in intramembranous ossification.

Authors:  Georgette N Jones; Daphne R Pringle; Zhirong Yin; Michelle M Carlton; Kimerly A Powell; Michael B Weinstein; Ramiro E Toribio; Krista M D La Perle; Lawrence S Kirschner
Journal:  Mol Endocrinol       Date:  2010-06-09

Review 3.  Ventrally emigrating neural tube (VENT) cells: a second neural tube-derived cell population.

Authors:  Douglas P Dickinson; Michal Machnicki; Mohammed M Ali; Zhanying Zhang; Gurkirpal S Sohal
Journal:  J Anat       Date:  2004-08       Impact factor: 2.610

4.  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 5.  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

6.  WNT/β-catenin signaling mediates human neural crest induction via a pre-neural border intermediate.

Authors:  Alan W Leung; Barbara Murdoch; Ahmed F Salem; Maneeshi S Prasad; Gustavo A Gomez; Martín I García-Castro
Journal:  Development       Date:  2016-02-01       Impact factor: 6.868

7.  Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein.

Authors:  Alissa M Hulstrand; Douglas W Houston
Journal:  Dev Biol       Date:  2013-08-29       Impact factor: 3.582

8.  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

Review 9.  Relations and interactions between cranial mesoderm and neural crest populations.

Authors:  Drew M Noden; Paul A Trainor
Journal:  J Anat       Date:  2005-11       Impact factor: 2.610

10.  Use of mutant mouse lines to investigate origin of gonadotropin-releasing hormone-1 neurons: lineage independent of the adenohypophysis.

Authors:  Hillery Metz; Susan Wray
Journal:  Endocrinology       Date:  2009-12-11       Impact factor: 4.736

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