Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptors

J Cell Biol. 2006 Apr 10;173(1):59-68. doi: 10.1083/jcb.200509036. Epub 2006 Apr 3.

Abstract

It is commonly assumed that photoreceptor (PR) outer segment (OS) morphogenesis is reliant upon the presence of peripherin/rds, hereafter termed Rds. In this study, we demonstrate a differential requirement of Rds during rod and cone OS morphogenesis. In the absence of this PR-specific protein, rods do not form OSs and enter apoptosis, whereas cone PRs develop atypical OSs and are viable. Such OSs consist of dysmorphic membranous structures devoid of lamellae. These tubular OSs lack any stacked lamellae and have reduced phototransduction efficiency. The loss of Rds only appears to affect the shape of the OS, as the inner segment and connecting cilium remain intact. Furthermore, these structures fail to associate with the specialized extracellular matrix that surrounds cones, suggesting that Rds itself or normal OS formation is required for this interaction. This study provides novel insight into the distinct role of Rds in the OS development of rods and cones.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Basic-Leucine Zipper Transcription Factors / genetics
  • Cell Differentiation / genetics*
  • Cell Survival / genetics
  • Electroretinography
  • Eye Proteins / genetics
  • Immunohistochemistry
  • Intermediate Filament Proteins / genetics*
  • Intracellular Membranes / metabolism
  • Intracellular Membranes / pathology
  • Intracellular Membranes / ultrastructure
  • Membrane Glycoproteins / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Microscopy, Electron, Transmission
  • Nerve Tissue Proteins / genetics*
  • Peripherins
  • Retinal Cone Photoreceptor Cells / abnormalities*
  • Retinal Cone Photoreceptor Cells / metabolism
  • Retinal Cone Photoreceptor Cells / ultrastructure
  • Retinal Rod Photoreceptor Cells / abnormalities*
  • Retinal Rod Photoreceptor Cells / metabolism
  • Retinal Rod Photoreceptor Cells / ultrastructure
  • Vision, Ocular / genetics

Substances

  • Basic-Leucine Zipper Transcription Factors
  • Eye Proteins
  • Intermediate Filament Proteins
  • Membrane Glycoproteins
  • Nerve Tissue Proteins
  • Nrl protein, mouse
  • Peripherins
  • Prph2 protein, mouse