Pigment epithelium-derived factor (PEDF) is an endogenous antiinflammatory factor

FASEB J. 2006 Feb;20(2):323-5. doi: 10.1096/fj.05-4313fje. Epub 2005 Dec 20.

Abstract

Pigment epithelium-derived factor (PEDF) is a potent angiogenic inhibitor. Reduced PEDF levels are associated with diabetic retinopathy. However, the mechanism for the protective effects of PEDF against diabetic retinopathy (DR) is presently unclear. As inflammation plays a role in DR, the present study determined the effect of PEDF on inflammation. Western blot analysis and ELISA demonstrated that retinal and plasma PEDF levels were drastically decreased in rats with endotoxin-induced uveitis (EIU), which suggests that PEDF is a negative acute-phase protein. Intravitreal injection of PEDF significantly reduced vascular hyper-permeability in rat models of diabetes and oxygen-induced retinopathy, correlating with the decreased levels of retinal inflammatory factors, including VEGF, VEGF receptor-2, MCP-1, TNF-alpha, and ICAM-1. In cultured retinal capillary endothelial cells, PEDF significantly decreased TNF-alpha and ICAM-1 expression under hypoxia. Moreover, down-regulation of PEDF expression by siRNA resulted in significantly increases of VEGF and TNF-alpha secretion in retinal Müller cells. These findings suggest that PEDF is a novel endogenous anti-inflammatory factor in the eye. The decrease of ocular PEDF levels may contribute to inflammation and vascular leakage in DR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / metabolism*
  • Anti-Inflammatory Agents / pharmacology
  • Cells, Cultured
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / pathology
  • Diabetic Retinopathy / complications
  • Diabetic Retinopathy / drug therapy
  • Diabetic Retinopathy / metabolism*
  • Down-Regulation
  • Endothelium / drug effects
  • Eye Proteins / metabolism*
  • Eye Proteins / pharmacology
  • Gene Expression Regulation
  • Lipopolysaccharides / toxicity
  • Nerve Growth Factors / metabolism*
  • Nerve Growth Factors / pharmacology
  • Oxygen / toxicity
  • Permeability
  • RNA Interference
  • Rats
  • Retina / cytology
  • Retinal Neovascularization / chemically induced
  • Retinal Neovascularization / drug therapy
  • Serpins / metabolism*
  • Serpins / pharmacology
  • Tumor Necrosis Factor-alpha / metabolism
  • Uveitis / chemically induced
  • Uveitis / drug therapy
  • Vascular Endothelial Growth Factor A / antagonists & inhibitors
  • Vascular Endothelial Growth Factor A / metabolism
  • Vascular Endothelial Growth Factor A / pharmacology
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism

Substances

  • Anti-Inflammatory Agents
  • Eye Proteins
  • Lipopolysaccharides
  • Nerve Growth Factors
  • Serpins
  • Tumor Necrosis Factor-alpha
  • Vascular Endothelial Growth Factor A
  • pigment epithelium-derived factor
  • Vascular Endothelial Growth Factor Receptor-2
  • Oxygen