PUBLICATION

Artery-vein specification in the zebrafish trunk is pre-patterned by heterogeneous Notch activity and balanced by flow-mediated fine tuning

Authors
Geudens, I., Coxam, B., Alt, S., Gebala, V., Vion, A.C., Meier, K., Rosa, A., Gerhardt, H.
ID
ZDB-PUB-190804-1
Date
2019
Source
Development (Cambridge, England)   146(16): (Journal)
Registered Authors
Coxam, Baptiste, Gerhardt, Holger, Meier, Katja, Rosa, Andre
Keywords
Angiogenesis, Artery, Developmental patterning, Haemodynamic, Notch, Vein
MeSH Terms
  • Animals
  • Arteries/embryology
  • Body Patterning*
  • Cell Polarity
  • Endothelial Cells/physiology
  • Genetic Heterogeneity
  • Lymphatic Vessels/embryology
  • Receptors, Notch/metabolism*
  • Regional Blood Flow
  • Signal Transduction
  • Veins/embryology
  • Zebrafish/blood
  • Zebrafish/embryology*
PubMed
31375478 Full text @ Development
Abstract
How developing vascular networks acquire the right balance of arteries, veins and lymphatic vessels to efficiently supply and drain tissues is poorly understood. In zebrafish embryos, the robust and regular 50:50 global balance of intersegmental veins and arteries that form along the trunk, prompts the intriguing question how the organism keeps "count". Previous studies suggest that the ultimate fate of an intersegmental vessel (ISV) is determined by the identity of the approaching secondary sprout emerging from the posterior cardinal vein (PCV). Here, we show that the formation of a balanced trunk vasculature involves an early heterogeneity in endothelial cell (EC) behavior and Notch signaling activity in the seemingly identical primary ISVs that is independent of secondary sprouting and flow. We show that Notch signaling mediates the local patterning of ISVs, and an adaptive flow-mediated mechanism subsequently fine-tunes the global balance of arteries and veins along the trunk. We propose that this dual mechanism provides the adaptability required to establish a balanced network of arteries, veins and lymphatic vessels.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping