Transcriptional regulation during development of the ductus arteriosus

Kathryn N. Ivey, David Sutcliffe, James Richardson, Ronald I. Clyman, Joseph A. Garcia, Deepak Srivastava

Research output: Contribution to journalArticle

30 Scopus citations

Abstract

The ductus arteriosus is a specialized blood vessel containing highly differentiated and contractile vascular smooth muscle, derived largely from neural crest cells, that is essential for fetal life but typically closes after birth. Impaired development of the ductus arteriosus or disruption of signaling pathways that initiate postnatal closure can result in persistent patency of the ductus arteriosus, the third most common congenital heart defect. We found that Tfap2β, a transcription factor associated with patent ductus arteriosus in humans, was uniquely expressed in mouse ductal smooth muscle. Endothelin-1 and the hypoxia-induced transcription factor, Hif2α were also highly enriched in ductal smooth muscle at embryonic day 13.5 and were dependent on Tfap2β for their expression in this domain. Hif2α functioned as a negative regulator of Tfap2β-induced transcription by disrupting protein-DNA interactions, suggesting a negative feedback loop regulating Tfap2β activity. Our data indicate that Tfap2β, Et-1, and Hif2α act in a transcriptional network during ductal smooth muscle development and that disruption of this pathway may contribute to patent ductus arteriosus by affecting the development of smooth muscle within the ductus arteriosus.

Original languageEnglish (US)
Pages (from-to)388-395
Number of pages8
JournalCirculation research
Volume103
Issue number4
DOIs
StatePublished - Aug 15 2008

Keywords

  • Ductus arteriosus
  • Endothelin-1
  • Hypoxia-inducible factor 1
  • Tfap2
  • Transcriptional regulation

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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