Evidence for two apoptotic pathways in light-induced retinal degeneration

Nat Genet. 2002 Oct;32(2):254-60. doi: 10.1038/ng984. Epub 2002 Sep 3.

Abstract

Excessive phototransduction signaling is thought to be involved in light-induced and inherited retinal degeneration. Using knockout mice with defects in rhodopsin shut-off and transducin signaling, we show that two different pathways of photoreceptor-cell apoptosis are induced by light. Bright light induces apoptosis that is independent of transducin and accompanied by induction of the transcription factor AP-1. By contrast, low light induces an apoptotic pathway that requires transducin. We also provide evidence that additional genetic factors regulate sensitivity to light-induced damage. Our use of defined mouse mutants resolves some of the complexity underlying the mechanisms that regulate susceptibility to retinal degeneration.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis*
  • Arrestin / genetics
  • Arrestin / metabolism
  • Carrier Proteins
  • Dexamethasone / metabolism
  • Eye Proteins*
  • G-Protein-Coupled Receptor Kinase 1
  • Light / adverse effects*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mutation
  • Photoreceptor Cells, Vertebrate / physiology
  • Protein Kinases / genetics
  • Protein Kinases / metabolism
  • Proteins / metabolism
  • Retina / metabolism
  • Retina / physiopathology
  • Retina / radiation effects*
  • Rhodopsin / metabolism
  • Signal Transduction
  • Transcription Factor AP-1 / antagonists & inhibitors
  • Transcription Factor AP-1 / metabolism
  • Transducin / metabolism
  • cis-trans-Isomerases

Substances

  • Arrestin
  • Carrier Proteins
  • Eye Proteins
  • Proteins
  • Transcription Factor AP-1
  • Dexamethasone
  • Rhodopsin
  • Protein Kinases
  • G-Protein-Coupled Receptor Kinase 1
  • Grk1 protein, mouse
  • retinoid isomerohydrolase
  • Transducin
  • cis-trans-Isomerases