
pmid: 11585794
Recent evidence indicates that acquisition of artery or vein identity during vascular development is governed, in part, by genetic mechanisms. The artery-specific expression of a number of Notch signaling genes in mouse and zebrafish suggests that this pathway may play a role in arterial-venous cell fate determination during vascular development. We show that loss of Notch signaling in zebrafish embryos leads to molecular defects in arterial-venous differentiation, including loss of artery-specific markers and ectopic expression of venous markers within the dorsal aorta. Conversely, we find that ectopic activation of Notch signaling leads to repression of venous cell fate. Finally, embryos lacking Notch function exhibit defects in blood vessel formation similar to those associated with improper arterial-venous specification. Our results suggest that Notch signaling is required for the proper development of arterial and venous blood vessels, and that a major role of Notch signaling in blood vessels is to repress venous differentiation within developing arteries.Movies available on-line
Embryonic Induction, Base Sequence, Microinjections, Molecular Sequence Data, Intracellular Signaling Peptides and Proteins, Gene Expression Regulation, Developmental, Membrane Proteins, Proteins, Receptor Protein-Tyrosine Kinases, Cell Differentiation, Ephrin-B2, Receptors, Cell Surface, Arteries, Proto-Oncogene Proteins, Mutation, Basic Helix-Loop-Helix Transcription Factors, Animals, Female, Receptors, Growth Factor, Biomarkers
Embryonic Induction, Base Sequence, Microinjections, Molecular Sequence Data, Intracellular Signaling Peptides and Proteins, Gene Expression Regulation, Developmental, Membrane Proteins, Proteins, Receptor Protein-Tyrosine Kinases, Cell Differentiation, Ephrin-B2, Receptors, Cell Surface, Arteries, Proto-Oncogene Proteins, Mutation, Basic Helix-Loop-Helix Transcription Factors, Animals, Female, Receptors, Growth Factor, Biomarkers
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