Absence of p53 delays apoptotic photoreceptor cell death in the rds mouse

Curr Eye Res. 1998 Sep;17(9):917-23. doi: 10.1076/ceyr.17.9.917.5137.


Purpose: This study was aimed at determining whether or not apoptotic photoreceptor cell death in a mouse model of inherited retinal degeneration is p53 dependent.

Methods: A colony of p53-deficient rds mice were obtained by crossing homozygous rds mice with animals homozygous for a targeted disruption of the p53 gene and genotyping the offspring of the F1 cross. Both parental strains were on a BALB/c background. Age matched p53-deficient rds mice and controls (p53-deficient, rds and BALB/c mice), were sacrificed from day 1 to day 58 after birth. Eyes were paraffin-embedded and a modified terminal dUTP nick-end labeling (TUNEL) technique was used to detect the number of cells displaying DNA fragmentation within the sectioned retina. Eyes were also resin-embedded for semi-thin and ultra-thin sectioning.

Results: The peak in photoreceptor apoptosis, which occurs at 16 days in the rds mouse, was delayed by 3 days in p53-deficient rds mice. In addition, there was also a delay in the loss of photoreceptor cells between 16 and 26 days. However, absence of p53 did not prevent retinal degeneration in the rds mouse. The number of photoreceptor cells in p53-deficient rds mice at 35 days was very similar to that in the controls.

Conclusions: We have demonstrated that absence of p53 delays but does not prevent photoreceptor cell loss in the rds mouse. Our results provide evidence for plasticity in the mechanism by which apoptosis proceeds in retinal degeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • DNA Primers / chemistry
  • Gene Deletion
  • Genes, p53*
  • Genotype
  • In Situ Nick-End Labeling
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Photoreceptor Cells, Vertebrate / pathology*
  • Photoreceptor Cells, Vertebrate / ultrastructure
  • Retina / pathology*
  • Retina / physiopathology
  • Retina / ultrastructure
  • Retinal Degeneration / genetics
  • Retinal Degeneration / pathology*
  • Retinal Degeneration / physiopathology
  • Tumor Suppressor Protein p53 / physiology*


  • DNA Primers
  • Tumor Suppressor Protein p53