Investigative Ophthalmology & Visual Science Cover Image for Volume 59, Issue 9
July 2018
Volume 59, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2018
Retinal amyloid pathology requires CD36 receptors.
Author Affiliations & Notes
  • Emily Plyler
    Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio, United States
    Biomedical Sciences, Kent State University, Kent, Ohio, United States
  • Matthew A Smith
    Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio, United States
  • Jason R Richardson
    Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio, United States
  • Christine M Dengler-Crish
    Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio, United States
  • Samuel D Crish
    Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, Ohio, United States
  • Footnotes
    Commercial Relationships   Emily Plyler, None; Matthew Smith, None; Jason Richardson, None; Christine Dengler-Crish, None; Samuel Crish, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2018, Vol.59, 3720. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Emily Plyler, Matthew A Smith, Jason R Richardson, Christine M Dengler-Crish, Samuel D Crish; Retinal amyloid pathology requires CD36 receptors.. Invest. Ophthalmol. Vis. Sci. 2018;59(9):3720.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose : Accumulation and aggregation of amyloid-beta, a neurotoxic protein associated with Alzheimer’s disease (AD), has been identified in retinas of glaucoma, age-related macular degeneration, and diabetic retinopathy. Moreover, the retina and optic nerve have been implicated as some of the earliest sites of pathology in AD, exhibiting amyloidosis prior to degeneration of the hippocampus and entorhinal cortex. However, the mechanism of amyloid deposition is not clear. Here, we sought to determine the potential role for cluster of differentiation 36 (CD36) on amyloid deposition and neuroinflammation in the retina and its projection.

Methods : Fibrillar, fluorophore-tagged amyloid-beta was unilaterally injected into the vitreal chamber of 6-8 month old C57BL/6J mice and transgenic mice lacking CD36. One or two weeks following injection, retinas, optic nerves, and their brain targets were evaluated by immunofluorescence and multiplex protein quantitation for inflammatory and neurodegenerative markers.

Results : Amyloid-beta produced neuroinflammation throughout the entire retinal projection - including distal brain targets. Retinal ganglion cell (RGC) degeneration was evident, with significant RGC reductions at 1 (77% of control) and 2 weeks (46% of control) after injection. Surprisingly, amyloid pathology was sectorial and spread to the opposite, un-injected retina and projection -- resulting in inflammation and RGC loss in the untreated eye. Amyloid-beta fibril injections in CD36-null mice did not produce significant neuroinflammatory responses or RGC loss.

Conclusions : Amyloid-beta fibrils produce spreading, sectorial inflammation and neurodegeneration in the absence of other stress factors in the retina and its projection. CD36 is necessary for amyloid-mediated neuroinflammation and acute degeneration.

This is an abstract that was submitted for the 2018 ARVO Annual Meeting, held in Honolulu, Hawaii, April 29 - May 3, 2018.

×
×

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.

×