12/15-Lipoxygenase gene knockout severely impairs ischemia-induced angiogenesis due to lack of Rac1 farnesylation

Blood. 2011 Nov 17;118(20):5701-12. doi: 10.1182/blood-2011-04-347468. Epub 2011 Aug 12.

Abstract

To understand the mechanisms by which 15(S)-hydroxyeicosatetraenoic acid (15(S)-HETE) activates Rac1 in the induction of angiogenesis, we studied the role of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase and αPix. 15(S)-HETE stimulated Rac1 in a sustained manner in human dermal microvascular endothelial cells (HDMVECs). Simvastatin, a potent inhibitor of HMG-CoA reductase, suppressed 15(S)-HETE-induced Rac1 activation in HDMVECs affecting their migration and tube formation. 15(S)-HETE by inducing HMG-CoA reductase expression caused increased farnesylation and membrane translocation of Rac1 where it became activated by Src-dependent αPix stimulation. Mevalonate rescued 15(S)-HETE-induced Rac1 farnesylation and membrane translocation in HDMVECs and the migration and tube formation of these cells from inhibition by simvastatin. Down-regulation of αPix inhibited 15(S)-HETE-induced HDMVEC migration and tube formation. Hind-limb ischemia induced Rac1 farnesylation and activation leading to increased angiogenesis and these effects were blocked by simvastatin and rescued by mevalonate in WT mice. In contrast, hind-limb ischemia failed to induce Rac1 farnesylation and activation as well as angiogenic response in 12/15-Lox(-/-) mice. Activation of Src and αPix were also compromised at least to some extent in 12/15-Lox(-/-) mice compared with WT mice in response to hind-limb ischemia. Together, these findings demonstrate for the first time that HMG-CoA reductase plays a determinant role in 12/15-Lox-induced angiogenesis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acyl Coenzyme A
  • Animals
  • Arachidonate 12-Lipoxygenase / genetics*
  • Arachidonate 12-Lipoxygenase / metabolism*
  • Arachidonate 15-Lipoxygenase / genetics*
  • Arachidonate 15-Lipoxygenase / metabolism*
  • Cell Movement / drug effects
  • Cell Movement / physiology
  • Cells, Cultured
  • Guanine Nucleotide Exchange Factors / metabolism
  • Hindlimb / blood supply
  • Humans
  • Hydroxyeicosatetraenoic Acids / antagonists & inhibitors
  • Hydroxyeicosatetraenoic Acids / metabolism
  • Hydroxymethylglutaryl CoA Reductases / genetics
  • Hydroxymethylglutaryl CoA Reductases / metabolism
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Ischemia / genetics*
  • Ischemia / physiopathology*
  • Mevalonic Acid / pharmacology
  • Mice
  • Mice, Knockout
  • Neovascularization, Physiologic / genetics*
  • Neuropeptides / metabolism*
  • Prenylation / drug effects
  • Prenylation / physiology
  • Rho Guanine Nucleotide Exchange Factors
  • Simvastatin / pharmacology
  • rac GTP-Binding Proteins / metabolism*
  • rac1 GTP-Binding Protein

Substances

  • 12-15-lipoxygenase
  • Acyl Coenzyme A
  • Guanine Nucleotide Exchange Factors
  • Hydroxyeicosatetraenoic Acids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Neuropeptides
  • Rac1 protein, mouse
  • Rho Guanine Nucleotide Exchange Factors
  • 3-hydroxy-3-methylglutaryl-coenzyme A
  • 15-hydroxy-5,8,11,13-eicosatetraenoic acid
  • Simvastatin
  • Hydroxymethylglutaryl CoA Reductases
  • Arachidonate 12-Lipoxygenase
  • Arachidonate 15-Lipoxygenase
  • rac GTP-Binding Proteins
  • rac1 GTP-Binding Protein
  • Mevalonic Acid