[HTML][HTML] Endothelin-1 regulates the dorsoventral branchial arch patterning in mice

H Ozeki, Y Kurihara, K Tonami, S Watatani… - Mechanisms of …, 2004 - Elsevier
H Ozeki, Y Kurihara, K Tonami, S Watatani, H Kurihara
Mechanisms of development, 2004Elsevier
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 …
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.
Elsevier