Cdc42 activation by endothelin regulates neural crest cell migration in the cardiac outflow tract

Research output: Contribution to journalArticle

Authors

External Institution(s)

  • Baylor College of Medicine

Details

Original languageEnglish (US)
Pages (from-to)795-812
Number of pages18
JournalDevelopmental Dynamics
Volume248
Issue number9
StatusPublished - Sep 1 2019
Peer-reviewedYes

Abstract

Background: Congenital cardiovascular malformations are the most common birth defects affecting children. Several of these defects occur in structures developing from neural crest cells. One of the key signaling pathways regulating cardiac neural crest cell (CNCC) development involves the endothelin-A receptor (Ednra). However, the exact function of Ednra signaling in CNCC is unknown. Results: The fate mapping of CNCC in Ednra embryos indicated that the migration of these cells is aberrant in the cardiac outflow tract (OFT), but not in the pharyngeal arches. This premature arrest of CNCC migration occurs independently of CNCC proliferation and apoptosis changes and major gene expression changes. Analysis of the Rho family of small GTPases in the mutant embryos revealed that Cdc42 failed to localize normally in the CNCC migrating in the OFT. The inhibition of Cdc42 activity in cultured embryos recapitulated the migratory phenotype observed in Ednra mice. Further analyses revealed that Cdc42 is part of the signaling pathway activated by endothelin specifically in OFT CNCC to control their migration. Conclusions: These results indicated that the activation of Cdc42 by endothelin signaling is important for CNCC migration in the OFT but this pathway is not involved in mandibular or pharyngeal arch artery patterning.

    Research areas

  • Cdc42, cardiovascular malformation, endothelin, fate mapping, migration, neural crest cell