Identification and characterization of a mirror-image oligonucleotide that binds and neutralizes sphingosine 1-phosphate, a central mediator of angiogenesis

Biochem J. 2014 Aug 15;462(1):153-62. doi: 10.1042/BJ20131422.

Abstract

The sphingolipid S1P (sphingosine 1-phosphate) is known to be involved in a number of pathophysiological conditions such as cancer, autoimmune diseases and fibrosis. It acts extracellularly through a set of five G-protein-coupled receptors, but its intracellular actions are also well documented. Employing in vitro selection techniques, we identified an L-aptamer (Spiegelmer®) to S1P designated NOX-S93. The binding affinity of NOX-S93 to S1P had a Kd value of 4.3 nM. The Spiegelmer® shows equal binding to dihydro-S1P, but no cross-reactivity to the related lipids sphingosine, lysophosphatidic acid, ceramide, ceramide-1-phosphate or sphingosine phosphocholine. In stably transfected CHO (Chinese-hamster ovary) cell lines expressing the S1P receptors S1PR1 or S1PR3, NOX-S93 inhibits S1P-mediated β-arrestin recruitment and intracellular calcium release respectively, with IC50 values in the low nanomolar range. The pro-angiogenic activity of S1P, and of the growth factors VEGF-A (vascular endothelial growth factor-A), FGF-2 (fibroblast growth factor-2) and IGF-1 (insulin-like growth factor-1), was effectively blocked by NOX-S93 in a cellular angiogenesis assay employing primary human endothelial cells. These data provide further evidence for the relevance of extracellular S1P as a central mediator of angiogenesis, suggesting pharmacological S1P neutralization as a promising treatment alternative to current anti-angiogenesis approaches.

MeSH terms

  • Angiogenesis Inhibitors / isolation & purification*
  • Angiogenesis Inhibitors / pharmacology
  • Animals
  • Aptamers, Nucleotide / pharmacology*
  • Arrestins / metabolism
  • CHO Cells
  • Calcium / metabolism
  • Cricetulus
  • Fibroblast Growth Factor 2 / antagonists & inhibitors
  • Humans
  • Insulin-Like Growth Factor I / antagonists & inhibitors
  • Lysophospholipids / antagonists & inhibitors*
  • Neovascularization, Pathologic
  • Receptors, Lysosphingolipid / metabolism
  • Sphingosine / analogs & derivatives*
  • Sphingosine / antagonists & inhibitors
  • Vascular Endothelial Growth Factor A / antagonists & inhibitors
  • beta-Arrestins

Substances

  • Angiogenesis Inhibitors
  • Aptamers, Nucleotide
  • Arrestins
  • Lysophospholipids
  • NOX-S93
  • Receptors, Lysosphingolipid
  • Vascular Endothelial Growth Factor A
  • beta-Arrestins
  • Fibroblast Growth Factor 2
  • sphingosine 1-phosphate
  • Insulin-Like Growth Factor I
  • Sphingosine
  • Calcium