PUBLICATION

Arteries are formed by vein-derived endothelial tip cells

Authors
Xu, C., Hasan, S.S., Schmidt, I., Rocha, S.F., Pitulescu, M.E., Bussmann, J., Meyen, D., Raz, E., Adams, R.H., Siekmann, A.F.
ID
ZDB-PUB-141217-19
Date
2014
Source
Nature communications   5: 5758 (Journal)
Registered Authors
Bussmann, Jeroen, Meyen, Dana, Raz, Erez, Siekmann, Arndt Friedrich
Keywords
none
MeSH Terms
  • Arteries/cytology
  • Arteries/growth & development*
  • Arteries/metabolism
  • Mice
  • Endothelial Cells/cytology
  • Endothelial Cells/metabolism*
  • Zebrafish/genetics
  • Zebrafish/metabolism
  • Signal Transduction
  • Retina/cytology
  • Retina/growth & development
  • Retina/metabolism
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
  • Veins/cytology
  • Veins/growth & development*
  • Veins/metabolism
  • Cell Lineage/genetics
  • Neovascularization, Physiologic*
  • Animals, Genetically Modified
  • Chemokine CXCL12/genetics
  • Chemokine CXCL12/metabolism
  • Gene Expression Regulation, Developmental
  • Animal Fins/blood supply
  • Animal Fins/cytology
  • Animal Fins/growth & development
  • Animal Fins/metabolism
  • Cell Movement
  • Endothelium, Vascular/cytology
  • Endothelium, Vascular/growth & development
  • Endothelium, Vascular/metabolism*
  • Receptors, CXCR4/genetics
  • Receptors, CXCR4/metabolism*
  • Time-Lapse Imaging
  • Animals
  • Video Recording
(all 36)
PubMed
25502622 Full text @ Nat. Commun.
Abstract
Tissue vascularization entails the formation of a blood vessel plexus, which remodels into arteries and veins. Here we show, by using time-lapse imaging of zebrafish fin regeneration and genetic lineage tracing of endothelial cells in the mouse retina, that vein-derived endothelial tip cells contribute to emerging arteries. Our movies uncover that arterial-fated tip cells change migration direction and migrate backwards within the expanding vascular plexus. This behaviour critically depends on chemokine receptor cxcr4a function. We show that the relevant Cxcr4a ligand Cxcl12a selectively accumulates in newly forming bone tissue even when ubiquitously overexpressed, pointing towards a tissue-intrinsic mode of chemokine gradient formation. Furthermore, we find that cxcr4a mutant cells can contribute to developing arteries when in association with wild-type cells, suggesting collective migration of endothelial cells. Together, our findings reveal specific cell migratory behaviours in the developing blood vessel plexus and uncover a conserved mode of artery formation.
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