Differential role of Jak-STAT signaling in retinal degenerations

FASEB J. 2006 Nov;20(13):2411-3. doi: 10.1096/fj.06-5895fje. Epub 2006 Sep 11.

Abstract

Retinal degeneration is a major cause of severe visual impairment or blindness. Understanding the underlying molecular mechanisms is a prerequisite to develop therapeutic approaches for human patients. We show in three mouse models that induced and inherited retinal degeneration induces LIF and CLC as members of the interleukin (IL)-6 family of proteins, activates proteins of the Jak-STAT signaling pathway, and up-regulates suppressors of cytokine signaling as a negative feedback loop. Inhibition of Jak2 leads to protection of photoreceptors in a model of induced but not in a model of inherited retinal degeneration. Differential activation of Akt suggests alternative pathways for cell death and/or survival in different models. Proteins induced during photoreceptor degeneration are not mainly expressed in photoreceptors but in cells of other retinal layers. This suggests a model in which photoreceptor injury is signaled to cells of the inner retina, which in turn initiate a response either to support viability or accelerate death of injured cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Interleukin-6 / metabolism
  • Light
  • Mice
  • Mice, Inbred BALB C
  • Photoreceptor Cells / physiology
  • Protein-Tyrosine Kinases / metabolism
  • Retinal Degeneration / pathology
  • Retinal Degeneration / physiopathology*
  • STAT Transcription Factors / physiology*
  • Signal Transduction

Substances

  • Interleukin-6
  • STAT Transcription Factors
  • Protein-Tyrosine Kinases