Literature DB >> 1292750

Expression of Hox 2.1 protein in restricted populations of neural crest cells and pharyngeal ectoderm.

S C Kuratani1, N A Wall.   

Abstract

A polyclonal antibody, alpha Hox 2.1a, was used to localize Hox 2.1 protein in presumptive neural crest cells and nodose ganglion of 8.5-10.0 day p.c. mouse embryos. The following results were obtained: (1) The nodose placode, in its epithelial state, first expresses Hox 2.1 protein at 9.0 d.p.c. By 9.5 d.p.c. presumptive migrating neuroblasts between the nodose placode and ganglion primordium also express Hox 2.1 protein. (2) At 9.5 d.p.c., presumptive crest cells lateral to the cephalic cardinal vein and within pharyngeal arches 4 and 6 are immunoreactive for alpha Hox 2.1a. In the arch 6 region, positive cells extend medially to a mesenchymal cell population on the lateral aspect of the foregut wall. (3) At 10.0 d.p.c., Hox 2.1 protein expression in putative crest cells is restricted to the arch 6 cell population. A similar staining pattern is seen using alpha Hox 2.1a with chick embryos. Comparison with the chicken embryo suggests that the Hox 2.1 positive cells in the pharyngeal arch and those on the lateral aspect of the foregut in the mouse embryo correspond to the caudalmost subpopulation of the circumpharyngeal crest (Kuratani and Kirby: Am. J. Anat. 191:215-227, 1991; Anat. Rec. 234:263-280, 1992). These results are consistent with a role for Hox 2.1 in pattern formation in the caudalmost region of the vertebrate head.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1292750     DOI: 10.1002/aja.1001950103

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  8 in total

1.  lessen encodes a zebrafish trap100 required for enteric nervous system development.

Authors:  Jacy Pietsch; Jean-Marie Delalande; Brett Jakaitis; James D Stensby; Sarah Dohle; William S Talbot; David W Raible; Iain T Shepherd
Journal:  Development       Date:  2006-01-05       Impact factor: 6.868

Review 2.  Genetic model system studies of the development of the enteric nervous system, gut motility and Hirschsprung's disease.

Authors:  G Burzynski; I T Shepherd; H Enomoto
Journal:  Neurogastroenterol Motil       Date:  2009-02       Impact factor: 3.598

Review 3.  Hox genes in the lung.

Authors:  C Kappen
Journal:  Am J Respir Cell Mol Biol       Date:  1996-08       Impact factor: 6.914

Review 4.  Migration and diversification of the vagal neural crest.

Authors:  Erica J Hutchins; Ezgi Kunttas; Michael L Piacentino; Aubrey G A Howard; Marianne E Bronner; Rosa A Uribe
Journal:  Dev Biol       Date:  2018-07-05       Impact factor: 3.582

5.  Endoderm-derived Sonic hedgehog and mesoderm Hand2 expression are required for enteric nervous system development in zebrafish.

Authors:  Bettina Reichenbach; Jean-Marie Delalande; Ekaterina Kolmogorova; Abigail Prier; Tu Nguyen; Chelsey M Smith; Jochen Holzschuh; Iain T Shepherd
Journal:  Dev Biol       Date:  2008-03-20       Impact factor: 3.582

6.  Perturbation of Hoxb5 signaling in vagal and trunk neural crest cells causes apoptosis and neurocristopathies in mice.

Authors:  M K M Kam; M C H Cheung; J J Zhu; W W C Cheng; E W Y Sat; P K H Tam; V C H Lui
Journal:  Cell Death Differ       Date:  2013-10-18       Impact factor: 15.828

Review 7.  Evolution and development of the fish jaw skeleton.

Authors:  April DeLaurier
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2018-10-31       Impact factor: 5.814

8.  HOXB5 cooperates with NKX2-1 in the transcription of human RET.

Authors:  Jiang Zhu; Maria-Mercedes Garcia-Barcelo; Paul Kwong Hang Tam; Vincent Chi Hang Lui
Journal:  PLoS One       Date:  2011-06-03       Impact factor: 3.240

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.