Suppression of Notch signalling by the COUP-TFII transcription factor regulates vein identity

Nature. 2005 May 5;435(7038):98-104. doi: 10.1038/nature03511.


Arteries and veins are anatomically, functionally and molecularly distinct. The current model of arterial-venous identity proposes that binding of vascular endothelial growth factor to its heterodimeric receptor--Flk1 and neuropilin 1 (NP-1; also called Nrp1)--activates the Notch signalling pathway in the endothelium, causing induction of ephrin B2 expression and suppression of ephrin receptor B4 expression to establish arterial identity. Little is known about vein identity except that it involves ephrin receptor B4 expression, because Notch signalling is not activated in veins; an unresolved question is how vein identity is regulated. Here, we show that COUP-TFII (also known as Nr2f2), a member of the orphan nuclear receptor superfamily, is specifically expressed in venous but not arterial endothelium. Ablation of COUP-TFII in endothelial cells enables veins to acquire arterial characteristics, including the expression of arterial markers NP-1 and Notch signalling molecules, and the generation of haematopoietic cell clusters. Furthermore, ectopic expression of COUP-TFII in endothelial cells results in the fusion of veins and arteries in transgenic mouse embryos. Thus, COUP-TFII has a critical role in repressing Notch signalling to maintain vein identity, which suggests that vein identity is under genetic control and is not derived by a default pathway.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Arteries / cytology
  • Arteries / metabolism
  • COUP Transcription Factor II
  • COUP Transcription Factors
  • Cell Differentiation*
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Endothelial Cells / metabolism
  • Endothelium, Vascular / metabolism
  • Gene Expression Regulation
  • Membrane Proteins / antagonists & inhibitors*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • Neuropilin-1 / metabolism
  • Organ Specificity
  • Receptors, Notch
  • Receptors, Steroid / deficiency
  • Receptors, Steroid / genetics
  • Receptors, Steroid / metabolism*
  • Signal Transduction*
  • Transcription Factors / deficiency
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Veins / cytology*
  • Veins / metabolism*


  • COUP Transcription Factor II
  • COUP Transcription Factors
  • DNA-Binding Proteins
  • Membrane Proteins
  • Nr2f2 protein, mouse
  • Receptors, Notch
  • Receptors, Steroid
  • Transcription Factors
  • Neuropilin-1