Granulocyte colony-stimulating factor protects retinal photoreceptor cells against light-induced damage

Invest Ophthalmol Vis Sci. 2008 Dec;49(12):5629-35. doi: 10.1167/iovs.08-1711. Epub 2008 Aug 1.

Abstract

Purpose: Granulocyte colony stimulating factor (G-CSF) has been shown to have neuroprotective and anti-inflammatory effects in cerebral damage models. In addition, bone-marrow-derived hematopoietic cells, which can be mobilized with G-CSF, have a neuroprotective effect in hereditary retinal cell death. The present study was conducted to investigate whether G-CSF protects photoreceptors from light-induced cell death.

Methods: G-CSF or vehicle was systemically injected before the light exposure and for four consecutive days after the exposure. Morphologic and electrophysiologic examinations were performed 1 week after the exposure to light. Gamma ray irradiation (6.5 Gy) was used to examine the involvement of bone marrow-derived cells increased by G-CSF injection. The expression of G-CSF receptor in the retina was analyzed by immunohistochemistry and quantitative RT-PCR.

Results: The outer nuclear layer thickness was partially preserved in G-CSF-treated mice (measured at 300 microm superior from the optic disc, G-CSF: 14.9 +/- 6.3 microm versus control: 6.7 +/- 2.5 microm), and an electroretinogram confirmed the preservation of wave amplitudes (maximum scotopic a-wave G-CSF: 97.7 +/- 48.0 microV versus control: 14.4 +/- 21.9 microV, maximum scotopic b-wave G-CSF: 298.1 +/- 145.3 microV versus control: 33.2 +/- 50.1 microV). The effect was not lost, even with leukocyte depletion by irradiation. G-CSF receptor was expressed in retinal cells and upregulated by the light exposure (1.8-fold upregulation 2 hours after light exposure).

Conclusions: G-CSF protects photoreceptor cells against light-induced damage, possibly via G-CSF receptor expressed on retinal cells. These findings may lead to a novel treatment strategy for neural degenerating diseases of the retina.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Cells / radiation effects
  • Electroretinography
  • Gamma Rays
  • Gene Expression
  • Granulocyte Colony-Stimulating Factor / administration & dosage*
  • Injections, Subcutaneous
  • Light
  • Lymphocyte Depletion
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Neuroprotective Agents / administration & dosage*
  • Photoreceptor Cells, Vertebrate / radiation effects*
  • Radiation Injuries, Experimental / genetics
  • Radiation Injuries, Experimental / physiopathology
  • Radiation Injuries, Experimental / prevention & control*
  • Receptors, Granulocyte Colony-Stimulating Factor / genetics
  • Receptors, Granulocyte Colony-Stimulating Factor / metabolism
  • Recombinant Proteins
  • Retinal Degeneration / genetics
  • Retinal Degeneration / physiopathology
  • Retinal Degeneration / prevention & control*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Up-Regulation
  • Whole-Body Irradiation

Substances

  • Neuroprotective Agents
  • Receptors, Granulocyte Colony-Stimulating Factor
  • Recombinant Proteins
  • Granulocyte Colony-Stimulating Factor