Increased isolevuglandin-modified proteins in glaucomatous astrocytes

Mol Vis. 2009 Jun 1:15:1079-91.

Abstract

Purpose: Lipid oxidation has been proposed to be a factor in the pathophysiology of glaucoma. We investigated whether elevated levels of isolevuglandin (iso[4]LGE(2)) protein adducts are associated with astrocytes derived from the glaucomatous optic nerve head. In addition, we examined whether the iso[4]LGE(2) protein adducts are altered following exposure of astrocytes to elevated pressure.

Methods: Astrocytes were isolated from rat brain cortex and human optic nerve and were subjected to pressure treatments, western blot analyses, liquid chromatography tandem mass spectrometry, and immunocytochemistry.

Results: Elevated levels of isolevuglandin (iso[4]LGE(2)) protein adducts were associated with astrocytes derived from the glaucomatous (n=10) optic nerve head when compared to those from controls (n=6). Astrocytes subjected to in vitro pressure treatment resulted in increased levels of iso[4]LGE(2) protein adducts. Pressure exposure and the recovery period affect iso[4]LGE(2) protein modification, and pyridoxamine was effective in decreasing the appearance of iso[4]LGE(2) protein adduct immunoreactivity when applied immediately after pressure treatment.

Conclusions: These results suggest that the elevated iso[4]LGE(2) protein adduct immunoreactivity observed in glaucomatous astrocytes may be due to chronic and/or prolonged exposure to pressure, and pyridoxamine may have prophylactic utility against such oxidative protein modification.

Publication types

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

MeSH terms

  • Aged
  • Aged, 80 and over
  • Animals
  • Astrocytes / metabolism*
  • Cerebral Cortex / cytology
  • Child
  • Fatty Acids, Unsaturated / metabolism*
  • Female
  • Glaucoma / metabolism*
  • Glaucoma / pathology
  • Humans
  • Lipid Peroxidation
  • Male
  • Middle Aged
  • Optic Disk / cytology
  • Oxidative Stress
  • Pressure
  • Protein Processing, Post-Translational / drug effects
  • Pyridoxamine / pharmacology
  • Rats

Substances

  • Fatty Acids, Unsaturated
  • iso(4)levuglandin E2
  • Pyridoxamine