Endothelin-1 regulates the dorsoventral branchial arch patterning in mice

Mech Dev. 2004 Apr;121(4):387-95. doi: 10.1016/j.mod.2004.02.002.

Abstract

Endothelin-1 (ET-1), a 21-amino acid peptide secreted by the epithelium and core mesenchyme in the branchial arches as well as vascular endothelium, is involved in craniofacial and cardiovascular development through endothelin receptor type-A (EdnrA) expressed in the neural crest-derived ectomesenchyme. Here we show that ET-1(-/-) mutant mice exhibit a homeotic-like transformation of the lower jaw to an upper jaw. Most of the maxillary arch-derived components are duplicated and replaced mandibular arch-derived structures, resulting in a mirror image of the upper and lower jaws in the ET-1(-/-) mutant. As for hyoid arch-derivatives, the ventral structures are severely affected in comparison to the dorsal ones in the ET-1(-/-) mutant. Correspondingly, the expression of Dlx5 and Dlx6, Distalless-related homeobox genes determining the ventral identity of the anterior branchial arches, and of the mandibular marker gene Pitx1 is significantly downregulated in the ET-1(-/-) mutant, whereas the expression of Dlx2 and the maxillary marker gene Prx2 is unaffected or rather upregulated. These findings indicate that the ET-1/EdnrA signaling may contribute to the dorsoventral axis patterning of the branchial arch system as a mediator of the regional intercellular interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Patterning / physiology*
  • Branchial Region / embryology*
  • Branchial Region / metabolism
  • Endothelin-1 / genetics
  • Endothelin-1 / metabolism*
  • Gene Expression / physiology
  • In Situ Hybridization
  • Mandible / abnormalities
  • Mandible / anatomy & histology
  • Mandible / embryology
  • Mice / embryology*
  • Mutation
  • Phenotype

Substances

  • Endothelin-1