Genome-wide expression profiling of the retinoschisin-deficient retina in early postnatal mouse development

Invest Ophthalmol Vis Sci. 2007 Feb;48(2):891-900. doi: 10.1167/iovs.06-0641.

Abstract

Purpose: The Rs1h knockout mouse displays retinal features typical for X-linked juvenile retinoschisis (RS). Consequently, this mouse line represents an excellent model to study early molecular events in RS.

Methods: Whole genome expression profiling using DNA-microarrays was performed on total RNA extracts from retinoschisin-deficient and wild-type murine retinas from postnatal days 7, 9, 11, and 14. Quantitative real-time RT-PCR (qRT-PCR) analysis of additional time points facilitated the refinement of the temporal expression profile of differentially regulated transcripts. Differential protein expression was confirmed by Western blot analysis.

Results: Based on biostatistic and knowledge-based DNA-microarray analyses we have identified differentially regulated retinal genes in early postnatal stages of the Rs1h-deficient mouse defining key molecular pathways including adhesion, cytoskeleton, vesicular trafficking, and immune response. A significant upregulation of Egr1 at P11 and several microglia/glia-related transcripts starting at P11 with a peak at P14 were identified in the diseased retina. The results provided evidence that macrophage/microglia activation precedes apoptotic photoreceptor cell death. Finally, the role of Egr1 in the pathogenesis of Rs1h-deficiency was investigated, and the results indicated that activation of the MAPK Erk1/2 pathway occurs as early as P7. Analyses of Rs1h(-/Y)/Egr1(-/-) double-knockout mice suggest that Egr1 upregulation is not a prerequisite for macrophage/microglia activation or apoptosis.

Conclusions: The findings imply that microglia/glia activation may be triggering events in the photoreceptor degeneration of retinoschisin-deficient mice. Furthermore, the data point to a role of Erk1/2-Egr1 pathway activation in RS pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Adhesion Molecules / physiology*
  • Disease Models, Animal
  • Early Growth Response Protein 1 / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Eye Proteins / physiology*
  • Gene Expression Profiling*
  • Gene Expression Regulation, Developmental*
  • Genome*
  • In Situ Nick-End Labeling
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microscopy, Fluorescence
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Retina / metabolism*
  • Retinoschisis / genetics*
  • Retinoschisis / metabolism
  • Retinoschisis / pathology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Up-Regulation

Substances

  • Cell Adhesion Molecules
  • Early Growth Response Protein 1
  • Egr1 protein, mouse
  • Eye Proteins
  • RS1 protein, mouse
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3