Triggering of Bcl-2-related pathway is associated with apoptosis of photoreceptors in Rpe65-/- mouse model of Leber's congenital amaurosis

Apoptosis. 2008 Mar;13(3):329-42. doi: 10.1007/s10495-008-0180-2.

Abstract

Mutations in RPE65 protein is characterized by the loss of photoreceptors, although the molecular pathways triggering retinal cell death remain largely unresolved. The role of the Bcl-2 family of proteins in retinal degeneration is still controversial. However, alteration in Bcl-2-related proteins has been observed in several models of retinal injury. In particular, Bax has been suggested to play a crucial role in apoptotic pathways in murine glaucoma model as well as in retinal detachment-associated cell death. We demonstrated that Bcl-2-related signaling pathway is involved in Rpe65-dependent apoptosis of photoreceptors during development of the disease. Pro-apoptotic Bax alpha and beta isoforms were upregulated in diseased retina. This was associated with a progressive reduction of anti-apoptotic Bcl-2, reflecting imbalanced Bcl-2/Bax ratio as the disease progresses. Moreover, specific translocation of Bax beta from cytosol to mitochondria was observed in Rpe65-deficient retina. This correlated with the initiation of photoreceptor cell loss at 4 months of age, and further increased during disease development. Altogether, these data suggest that Bcl-2-apoptotic pathway plays a crucial role in Leber's congenital amaurosis disease. They further highlight a new regulatory mechanism of Bax-dependent apoptosis based on regulated expression and activation of specific isoforms of this protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Blindness / congenital
  • Blindness / genetics*
  • Blindness / physiopathology
  • Carrier Proteins / genetics*
  • Cell Line
  • Disease Models, Animal
  • Eye Proteins / genetics*
  • Gene Expression Regulation
  • Humans
  • In Situ Nick-End Labeling
  • Mice
  • Mitochondria / metabolism
  • Photoreceptor Cells / cytology*
  • Protein Conformation
  • Protein Transport
  • Proto-Oncogene Proteins c-bcl-2 / physiology*
  • Retina / metabolism*
  • Up-Regulation
  • bcl-2-Associated X Protein / biosynthesis
  • bcl-2-Associated X Protein / physiology*
  • cis-trans-Isomerases

Substances

  • Carrier Proteins
  • Eye Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • retinoid isomerohydrolase
  • cis-trans-Isomerases