Endoplasmic reticulum stress in human photoreceptor diseases

Brain Res. 2016 Oct 1;1648(Pt B):538-541. doi: 10.1016/j.brainres.2016.04.021. Epub 2016 Apr 23.

Abstract

Photoreceptors are specialized sensory neurons essential for light detection in the human eye. Photoreceptor cell dysfunction and death cause vision loss in many eye diseases such as retinitis pigmentosa and achromatopsia. Endoplasmic reticulum (ER) stress and Unfolded Protein Response (UPR) signaling have been implicated in the development and pathology of heritable forms of retinitis pigmentosa and achromatopsia. We review the role of ER stress and UPR in retinitis pigmentosa arising from misfolded rhodopsins (RHO) and in achromatopsia arising from genetic mutations in Activating Transcription Factor 6 (ATF6). This article is part of a Special Issue entitled SI:ER stress.

Keywords: ATF6; Achromatopsia; Photoreceptor; Retina; Retinitis pigmentosa; Rhodopsin.

Publication types

  • Review

MeSH terms

  • Activating Transcription Factor 6 / genetics
  • Endoplasmic Reticulum Stress / genetics
  • Endoplasmic Reticulum Stress / physiology*
  • Humans
  • Mutation / genetics
  • Photoreceptor Cells, Vertebrate / pathology*
  • Photoreceptor Cells, Vertebrate / physiology*
  • Retinal Diseases / genetics
  • Retinal Diseases / pathology*
  • Retinal Diseases / physiopathology
  • Unfolded Protein Response / genetics
  • Unfolded Protein Response / physiology

Substances

  • ATF6 protein, human
  • Activating Transcription Factor 6