Photoreceptor protection by cardiotrophin-1 in transgenic rats with the rhodopsin mutation s334ter

Invest Ophthalmol Vis Sci. 2003 Sep;44(9):4069-75. doi: 10.1167/iovs.02-1130.

Abstract

Purpose: This work examines the effects of cardiotrophin (CT)-1 on photoreceptor survival in transgenic rats that carry the rhodopsin mutation S334ter.

Methods: Recombinant CT-1 was injected intravitreally into eyes of heterozygous animals. Photoreceptor survival was analyzed by histology. Phosphorylation of signal transducer and activator of transcription1 (STAT1), STAT3, extracellular signal-regulated kinase (ERK), or Akt was assessed by immunoblot analysis. Localization of phosphorylated STAT3 was determined by immunocytochemistry.

Results: Heterozygous S334ter rats experience rapid photoreceptor degeneration. By postnatal day (PD)20, the outer nuclear layer (ONL) retained only 1 to 2 rows of nuclei compared with 10 to 12 rows in wild-type animals. Repeated administration of CT-1 resulted in significant survival of photoreceptors. At PD20, a CT-1-treated eye (2 micro g/2 micro L every 3 days, starting at PD9) had six to seven rows of nuclei, and the vehicle-treated eyes had only one to two rows. At PD30, eyes treated every 3 days still had five to six rows of nuclei, in contrast to no rows to one row in vehicle-treated eyes. Eyes treated every 4 days retained three to four rows, whereas eyes treated every 5 days had two to three rows. There was a significant increase in phosphorylated STAT1 and -3 in the retina after CT-1 injection. The increase in phosphorylated STAT3 was colocalized with glutamine synthetase, a Müller cell marker, by immunocytochemistry.

Conclusions: These results indicate that CT-1 promotes photoreceptor survival and that Müller cells probably mediate this effect. They also suggest that sustained delivery of the protein is essential for long-term rescue of photoreceptors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Cell Survival / drug effects
  • Cytokines / therapeutic use*
  • Cytoprotection / drug effects
  • DNA-Binding Proteins / metabolism
  • Fluorescent Antibody Technique, Indirect
  • Immunoblotting
  • Immunoenzyme Techniques
  • Injections
  • Mitogen-Activated Protein Kinases / metabolism
  • Mutation*
  • Phosphorylation
  • Photoreceptor Cells, Vertebrate / drug effects*
  • Photoreceptor Cells, Vertebrate / metabolism
  • Photoreceptor Cells, Vertebrate / pathology
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins
  • Retinal Degeneration / genetics
  • Retinal Degeneration / metabolism
  • Retinal Degeneration / pathology
  • Retinal Degeneration / prevention & control*
  • Rhodopsin / genetics*
  • STAT3 Transcription Factor
  • Trans-Activators / metabolism
  • Vitreous Body

Substances

  • Cytokines
  • DNA-Binding Proteins
  • Proto-Oncogene Proteins
  • Recombinant Proteins
  • STAT3 Transcription Factor
  • Stat3 protein, rat
  • Trans-Activators
  • Rhodopsin
  • cardiotrophin 1
  • Akt1 protein, rat
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinases