Encyclopedia of Computational Neuroscience

Living Edition
| Editors: Dieter Jaeger, Ranu Jung

Retinal Disease and Remodeling

  • Robert E. MarcEmail author
Living reference work entry
DOI: https://doi.org/10.1007/978-1-4614-7320-6_659-1


Retinal remodeling is a collection of pathologic changes in the structure and function of the neural retina triggered by photoreceptor degenerations.

Detailed Description

Diseases That Cause Retinal Remodeling

Retinal remodeling is initiated by inherited gene defects and gene-risk coupled environmental stressors that lead to photoreceptor degeneration (Jones et al. 2003, 2012; Marc et al. 2003), e.g., retinitis pigmentosa (RP) and macular degeneration (AMD). Over 100 gene loci are associated with RP-like degenerations (Daiger and Sullivan 2013). Most RP-like degenerations directly affect rods, leaving many cones intact. Rod death can, however, trigger extensive bystander killing of cones. These different effects have been classified as cone sparing and cone decimating (Marc et al. 2007). After photoreceptor death, the surviving retina progressively changes form and signaling properties. Remodeling progression depends on the nature of the primary degeneration. Recessive RP...


Retinitis Pigmentosa Bipolar Cell Retinoic Acid Receptor Outer Nuclear Layer Retinal Pigment Epithelium 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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Copyright information

© Springer Science+Business Media New York 2014

Authors and Affiliations

  1. 1.John A. Moran Eye CenterUniversity of UtahSalt Lake CityUSA