Role of glutamine and interlinked asparagine metabolism in vessel formation

EMBO J. 2017 Aug 15;36(16):2334-2352. doi: 10.15252/embj.201695518. Epub 2017 Jun 28.

Abstract

Endothelial cell (EC) metabolism is emerging as a regulator of angiogenesis, but the precise role of glutamine metabolism in ECs is unknown. Here, we show that depriving ECs of glutamine or inhibiting glutaminase 1 (GLS1) caused vessel sprouting defects due to impaired proliferation and migration, and reduced pathological ocular angiogenesis. Inhibition of glutamine metabolism in ECs did not cause energy distress, but impaired tricarboxylic acid (TCA) cycle anaplerosis, macromolecule production, and redox homeostasis. Only the combination of TCA cycle replenishment plus asparagine supplementation restored the metabolic aberrations and proliferation defect caused by glutamine deprivation. Mechanistically, glutamine provided nitrogen for asparagine synthesis to sustain cellular homeostasis. While ECs can take up asparagine, silencing asparagine synthetase (ASNS, which converts glutamine-derived nitrogen and aspartate to asparagine) impaired EC sprouting even in the presence of glutamine and asparagine. Asparagine further proved crucial in glutamine-deprived ECs to restore protein synthesis, suppress ER stress, and reactivate mTOR signaling. These findings reveal a novel link between endothelial glutamine and asparagine metabolism in vessel sprouting.

Keywords: angiogenesis; asparagine; endothelial cell; glutamine; metabolism.

MeSH terms

  • Asparagine / metabolism*
  • Cell Movement / drug effects*
  • Cell Proliferation / drug effects*
  • Culture Media / chemistry
  • Endothelial Cells / drug effects*
  • Endothelial Cells / metabolism
  • Endothelial Cells / physiology*
  • Glutaminase / metabolism
  • Glutamine / metabolism*
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Metabolic Networks and Pathways
  • Neovascularization, Pathologic
  • Neovascularization, Physiologic / drug effects*

Substances

  • Culture Media
  • Glutamine
  • Asparagine
  • GLS protein, human
  • Glutaminase