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Role of Endothelial Cell Metabolism in Vessel Sprouting

Journal

CELL METABOLISM
Volume 18, Issue 5, Pages 634-647

Publisher

CELL PRESS
DOI: 10.1016/j.cmet.2013.08.001

Keywords

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Funding

  1. Research Foundation Flanders (FWO)
  2. Flemish Association against Cancer
  3. Federal Government Belgium grant [IUAP07/03]
  4. Flemish Government
  5. Concerted Research Activities Belgium grant [GOA2006/11]
  6. FWO [G.0652.08, G.0692.09, G.0532.10, G.0817.11, 1.5.202.10.N.00]
  7. Foundation Leducq Transatlantic Network
  8. European Research Council Advanced Research Grant [EU-ERC269073]

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Endothelial cells (ECs) are quiescent for years but can plastically switch to angiogenesis. Vascular sprouting relies on the coordinated activity of migrating tip cells at the forefront and proliferating stalk cells that elongate the sprout. Past studies have identified genetic signals that control vascular branching. Prominent are VEGF, activating tip cells, and Notch, which stimulates stalk cells. After the branch is formed and perfused, ECs become quiescent phalanx cells. Now, emerging evidence has accumulated indicating that ECs not only adapt their metabolism when switching from quiescence to sprouting but also that metabolism regulates vascular sprouting in parallel to the control by genetic signals.

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