Abstract

Summary

This thesis characterizes retinal neuronal remodelling in a mouse model of autosomal dominant optic atrophy, finding progressive dendritic atrophy in retinal ganglion cells (RGCs) and reduced glutamatergic synaptic connectivity specifically in ON-centre RGCs. These findings are relevant to lighting design because ON-centre RGCs include intrinsically photosensitive cells (ipRGCs) critical for circadian photoentrainment, meaning optic atrophy patients may have compromised non-visual light responses.
Abstract

Key Findings

  • 50% reduction in Opa1 transcript and protein in the B6;C3-Opa1Q285STOP heterozygous mouse model
  • Retinal ganglion cell dendritic atrophy was localized exclusively to sublamina b of the inner plexiform layer and was exacerbated with age
  • Marked reduction in glutamatergic synaptic sites and PSD95 levels specifically on ON-centre retinal ganglion cells
  • Significant increase in synaptic vesicle number and density in both ON and OFF bipolar cells
Categories

Categories

Eye Health & Vision: Investigates retinal ganglion cell degeneration and structural changes in the retina in a mouse model of optic atrophy, directly relevant to retinal health and vision loss.
The Science of Light: Examines retinal ganglion cell architecture and synaptic connectivity, including changes to ON-centre RGCs which are relevant to photoreceptor and ipRGC biology.
Authors

Author(s)

P Williams
Publication Date

Publication Year

2011
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