The overall goal of this project is to understand how retinal computations are modified in response to the structure of the visual environment. It has long been known that the sensitivity of retinal ganglion cells (RGCs) is depen- dent on recent visual input. These adaptive changes in sensitivity show remarkable flexibility; some RGCs adapt to ignore predictable components of the visual world in favor of encoding what is unexpected. This strategy is thought to maximize the amount of information transmitted to the higher brain. Recent work from our lab, how- ever, suggests that some RGCs use previous visual stimuli to predict future input. High-contrast input to these RGCs, such as a moving object, increases their sensitivity, thereby encoding the object's likely future location. It remais unknown, however, whether RGCs sensitize to properties of the visual environment beyond luminance and contrast, or, more simply, whether the retina maintains predictions about more complex features of the visual world. The first goal of this work is to understand the class of visual features to which the retina exhibits predictive sensitization. A second goal is to take advantage of the tractability of the retina to explore the neural mechanisms underlying prediction, a computation thought to be performed throughout the brain. In addition to improving our fundamental understanding of the retina, these results will have direct application. Retinal prosthetic devices hold the promise of substantially restored vision for those suffering from photoreceptor degeneration diseases, which affect more than two million Americans. As the computation of predictive sensitization is easily implemented in digital circuits, this research wil provide basic scientific insight and computational models to inform in the design of processing elements in retinal prosthetics.

Public Health Relevance

Nearly two million Americans suffer from age-related macular degeneration, only one of many retinal diseases leading to vision loss. For these patients, retinal prosthetic devices may substantially restore lost vision and lead to dramatic quality of lie improvements. This research will explore the neural mechanisms by which the retina changes its processing strategies to better suit a changing visual environment, and will directly aid in th design of processing components for retinal prosthetics.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31EY025110-02
Application #
9020092
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Agarwal, Neeraj
Project Start
2015-01-02
Project End
2018-01-01
Budget Start
2016-01-03
Budget End
2017-01-02
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Stanford University
Department
Neurology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94304