Type I pig collagen enhances the efficacy of PEDF 34-mer peptide in a mouse model of laser-induced choroidal neovascularization

Graefes Arch Clin Exp Ophthalmol. 2019 Aug;257(8):1709-1717. doi: 10.1007/s00417-019-04394-z. Epub 2019 Jun 20.

Abstract

Background: Pigment epithelium-derived factor (PEDF)-derived 34-mer peptide (PEDF34, Asp44-Asn77) has anti-angiogenic activity but has limitations in clinical application because of an inverted bell-shaped dose-effect relationship and a short half-life. In this study, we attempted to mitigate these problems by mixing PEDF34 with type I collagen.

Methods: The anti-angiogenic activity of the PEDF34/atelocollagen mixture was evaluated by HUVEC tube formation assay and in a laser-induced choroidal neovascular (CNV) mouse model. PEDF34 and/or collagen were administrated using intravitreal injections or eye drops. CNV lesion size was quantified using FITC-dextran-perfused retinal whole mounts. Western blot analysis and inhibitor assays were used to define the action mechanisms of PEDF34 and the mixture.

Results: Collagen broadened the effective dose range of PEDF34 in the tube formation assay by > 250 times (from 0.2 to 50 nM). In the CNV model, five intravitreal injections of PEDF34 were required for therapeutic effect, whereas the mixture had a significant therapeutic effect following a single injection. Eye drops of the mixture showed significantly stronger CNV-suppressive effects than drops of PEDF34 alone. The anti-angiogenic activity of PEDF34 might be mediated by inhibition of ERK and JNK activation by VEGF, and collagen potentiated these effects.

Conclusions: Collagen can serve as a carrier and reservoir of PEDF34. PEDF peptide/collagen mixture is easy to prepare than conventional methods for maintaining the therapeutic effect of PEDF peptide.

Keywords: Anti-angiogenesis effect; Choroidal neovascularization; Pigment epithelium-derived factor; Type I collagen.

MeSH terms

  • Animals
  • Cells, Cultured
  • Choroid / pathology*
  • Choroidal Neovascularization / drug therapy*
  • Choroidal Neovascularization / metabolism
  • Choroidal Neovascularization / pathology
  • Collagen Type I / administration & dosage*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Eye Proteins / administration & dosage*
  • Female
  • Humans
  • Lasers / adverse effects
  • Mice
  • Mice, Inbred C57BL
  • Nerve Growth Factors / administration & dosage*
  • Ophthalmic Solutions
  • Protease Inhibitors / administration & dosage
  • Retina / pathology
  • Serpins / administration & dosage*

Substances

  • Collagen Type I
  • Eye Proteins
  • Nerve Growth Factors
  • Ophthalmic Solutions
  • Protease Inhibitors
  • Serpins
  • pigment epithelium-derived factor

Grants and funding