Blockade of insulin receptor substrate-1 inhibits corneal lymphangiogenesis

Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5778-85. doi: 10.1167/iovs.10-6816.

Abstract

Purpose: To analyze whether insulin receptor substrate (IRS-1) is involved in lymphatic vessel development and whether IRS-1 blockade can inhibit lymphangiogenesis in vivo.

Methods: The impact of IRS-1 blockade by GS-101 (Aganirsen), an antisense oligonucleotide against IRS-1, on lymphatic endothelial cell (LEC) proliferation was assessed by ELISA. Furthermore, the effect of IRS-1 blockade on prolymphangiogenic growth factor expression by LECs and macrophages (peritoneal exudate cells) was tested by real-time PCR. The mouse model of inflammatory corneal neovascularization was used to analyze the effect of IRS-1 blockade in vivo: after corneal suture placement, mice were treated with GS-101 eye drops (twice daily afterwards for 1 week, 5 μL per drop; 50, 100, or 200 μM). Afterward, corneal wholemounts were prepared and stained for blood and lymphatic vessels.

Results: Blockade of IRS-1 by GS-101 inhibited LEC proliferation dose dependently. GS-101 led to decreased VEGF-A expression levels in LECs, whereas VEGF-C, VEGF-D, and VEGFR3 showed no significant change. In macrophages, VEGF-A expression levels were also inhibited by IRS-1 blockade. Additionally, GS-101 strongly inhibited macrophage-derived VEGF-C, VEGF-D, and VEGFR3 expression. In vivo, corneal hemangiogenesis was significantly inhibited when used at a concentration of 200 μM (by 17%; P < 0.01). Corneal lymphangiogenesis was significantly inhibited when used at a dose of 100 μM (by 21%; P < 0.01), and the highest used dose (200 μM) showed an even stronger inhibition (by 28%; P < 0.001).

Conclusions: Blockade of IRS-1 inhibits not only hemangiogenesis but also lymphangiogenesis. To the authors' knowledge, this is the first evidence that IRS-1 is involved in the molecular pathway leading to lymphangiogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division / physiology
  • Cells, Cultured
  • Endothelial Cells / cytology
  • Endothelial Cells / physiology*
  • Endothelium, Corneal / cytology
  • Endothelium, Corneal / physiology*
  • Female
  • Humans
  • Insulin Receptor Substrate Proteins / antagonists & inhibitors
  • Insulin Receptor Substrate Proteins / genetics
  • Insulin Receptor Substrate Proteins / physiology*
  • Lymphangiogenesis / physiology*
  • Macrophages, Peritoneal / cytology
  • Macrophages, Peritoneal / physiology*
  • Mice
  • Oligonucleotides / pharmacology
  • Ophthalmic Solutions
  • Signal Transduction / physiology
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor C / genetics
  • Vascular Endothelial Growth Factor D / genetics
  • Vascular Endothelial Growth Factor Receptor-3 / genetics

Substances

  • GS 101
  • IRS1 protein, human
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • Oligonucleotides
  • Ophthalmic Solutions
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factor C
  • Vascular Endothelial Growth Factor D
  • vascular endothelial growth factor A, mouse
  • Vascular Endothelial Growth Factor Receptor-3