Tetrapeptide AcSDKP induces postischemic neovascularization through monocyte chemoattractant protein-1 signaling

Arterioscler Thromb Vasc Biol. 2006 Apr;26(4):773-9. doi: 10.1161/01.ATV.0000203510.96492.14. Epub 2006 Jan 12.

Abstract

Background: We investigated the putative proangiogenic activity and molecular pathway(s) of the tetrapeptide acetyl-N-Ser-Asp-Lys-Pro (AcSDKP) in a model of surgically induced hindlimb ischemia.

Methods and results: Hindlimb ischemia was induced by femoral artery ligature and an osmotic minipump was implanted subcutaneously to deliver low (0.12 mg/kg per day) or high (1.2 mg/kg per day) doses of AcSDKP, for 7 or 21 days. Angiography scores, arteriole density, capillary number, and foot perfusion were increased at day 21 in the high-dose AcSDKP-treated mice (by 1.9-, 1.8-, 1.3-, and 1.6-fold, respectively) compared with control animals (P<0.05, P<0.01, P<0.01, respectively). AcSDKP treatment for 24 hours upregulated the monocyte chemoattractant protein-1 (MCP-1) mRNA and protein levels by 1.5-fold in cultured endothelial cells (P<0.01). In the ischemic hindlimb model, administration of AcSDKP also enhanced MCP-1 mRNA levels by 90-fold in ischemic leg (P<0.001) and MCP-1 plasma levels by 3-fold (P<0.001 versus untreated ischemic control mice). MCP-1 levels upregulation were associated with a 2.3-fold increase in the number of Mac3-positive cells in ischemic area of AcSDKP-treated mice (P<0.001 versus untreated animals). Interestingly, AcSDKP-induced monocyte/macrophage infiltration and postischemic neovascularization was fully blunted in MCP-1-deficient animals.

Conclusions: AcSDKP stimulates postischemic neovascularization through activation of a proinflammatory MCP-1-related pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Cells / pathology
  • Cell Differentiation
  • Cell Line, Transformed
  • Chemokine CCL2 / deficiency
  • Chemokine CCL2 / physiology*
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / pathology
  • Femoral Artery / pathology
  • Hindlimb / blood supply*
  • Ischemia / drug therapy*
  • Ischemia / physiopathology
  • Mice
  • Mice, Inbred C57BL
  • Monocytes / pathology
  • Neovascularization, Physiologic / drug effects*
  • Oligopeptides / administration & dosage*
  • Signal Transduction / drug effects

Substances

  • Chemokine CCL2
  • Oligopeptides
  • goralatide