April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Visual phenotyping of Wfs1 mutant mice, models of Wolfram syndrome neuronal and diabetic symptoms
Author Affiliations & Notes
  • Cecile Delettre
    INSERM U1051, Montpellier, France
  • Christian P Hamel
    INSERM U1051, Montpellier, France
  • Sulev Koks
    University of Tartu, Tartu, Estonia
  • Marie Seveno
    INSERM U1051, Montpellier, France
  • Guy Lenaers
    INSERM U1051, Montpellier, France
  • Delphine M Bonnet Wersinger
    INSERM U1051, Montpellier, France
  • Footnotes
    Commercial Relationships Cecile Delettre, None; Christian Hamel, None; Sulev Koks, None; Marie Seveno, None; Guy Lenaers, None; Delphine Bonnet Wersinger, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 6177. doi:https://doi.org/
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      Cecile Delettre, Christian P Hamel, Sulev Koks, Marie Seveno, Guy Lenaers, Delphine M Bonnet Wersinger; Visual phenotyping of Wfs1 mutant mice, models of Wolfram syndrome neuronal and diabetic symptoms. Invest. Ophthalmol. Vis. Sci. 2014;55(13):6177. doi: https://doi.org/.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: Wolfram syndrome is an early onset genetic disease (1/160,000) featuring diabetes mellitus and optic neuropathy, associated to mutation in the WFS1 gene. Mouse model with deleted exon 8 of Wolframin shows pancreatic beta cell atrophy, but its visual performance has not been investigated, prompting us to study its visual function and the histopathology of the retina and optic nerve.

Methods: Electroretinogram (ERG, retinal function) and visual evoked potentials (VEPs, visual pathway) were performed in Wfs1-/- and Wfs1+/+ mice at 3, 6 and 9 months of age. Fundi were pictured with Micron III apparatus. Retinal ganglion cell (RGC) proportion was determined from Brn3a immuno-labeling of retinal sections. RGC axonal loss was quantified by electron microscopy in transversal optic nerve sections.

Results: ERG showed a sex-dependent alteration in Wfs1 mutant mice at 3 months. Photoreceptor response amplitude (a-wave) was increased by 25.5% by Wfs1 mutation in females, while reduced by 28.2% in males. In contrast, positive scotopic threshold responses (pSTR) at the same age were found increased in mutant group by 20.5%. A preliminary study of 7 months male samples showed a severe loss of RGC somas (-50%) and axons in retina and optic nerve respectively. Finally, 7-8 months knocked-in mice presented a severe ocular hypertension.

Conclusions: Electrophysiological phenotyping of Wfs1 deleted mouse exon 8 visual function indicate a significant loss of RGC in mutant mouse at 7 month. Structural analysis of retinal ganglion cell somas and axons are conducted to characterize optic neuropathy in these animals.

Keywords: 531 ganglion cells • 613 neuro-ophthalmology: optic nerve  
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