April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Age-Related Dendrite Pruning in the Adult Brown Norway (BN) Rat Retina
Author Affiliations & Notes
  • L. Kisiswa
    School of Optometry and Vision Sciences, Cardiff University, Cardiff, United Kingdom
  • J. Albon
    School of Optometry and Vision Sciences, Cardiff University, Cardiff, United Kingdom
  • M. A. Wride
    Zoology Department, University of Dublin Trinity College, Dublin, Ireland
  • J. E. Morgan
    Ophthalmology, University Hospital of Wales, Cardiff, United Kingdom
  • Footnotes
    Commercial Relationships  L. Kisiswa, None; J. Albon, None; M.A. Wride, None; J.E. Morgan, None.
  • Footnotes
    Support  National Eye Research Centre (NERC), UK, Grant RCOP256
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 4050. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      L. Kisiswa, J. Albon, M. A. Wride, J. E. Morgan; Age-Related Dendrite Pruning in the Adult Brown Norway (BN) Rat Retina. Invest. Ophthalmol. Vis. Sci. 2010;51(13):4050.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose: : To determine the extent in which age-related dendritic pruning occurs in the adult rat retina.

Methods: : Whole-mount retinal explants from 6 (young) and 24-52 weeks (mature) old BN rats were prepared and RGCs were diolisticaly (DiI) labelled using BioRad gene gun and Hoeschst 33342. Changes in RGC dendritic complexity were assessed utilising Sholl analysis. RGC cell density was determined in the whole mounts while outer and inner nuclear layer (ONL and INL) cell number was assessed in retinal slices stained with Hoeschst 33342

Results: : RGC dendrite branching was significantly reduced (p<0.0002) in 24-52 compared to 6 weeks old RGCs, although dendrite length remained unchanged. There was marginal RGC loss (7%) in mature compared to young retinae. RGC density was significantly reduced (p<0.001) (26%) in the central (1mm from optic disc), but not in the peripheral (2-3mm from the optic disc) retina of 24-52 compared to 6 weeks old BN retina. Overall retinal area was significantly increased (p<0.001) (23%) in mature compared to younger BN retina. A significant reduction in the INL and ONL cell numbers were also significantly reduced (p<0.001 and p<0.001 respectively (25% and 20% respectively)) occurred in mature retina although there was no evidence of thinning of the layers.

Conclusions: : Age-related reduction in RGC dendritic complexity implies that dendritic pruning occurs during adulthood. Developmental retinal expansion that occurs during the period studied, which accounts, in part for the reduction in RGC density, suggests that cell loss is marginal. Age-related dendritic modifications should be considered when determining the effects of disease models in RGC morphology.

Keywords: ganglion cells • aging • degenerations/dystrophies 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×