Ganglion cells (GCs) and other inner retinal neurons are fundamental to retinal neural circuitry, processing photoreceptor signals relayed from intermediate neurons for transmission to the brain. Yet, much remains unknown about their role in vision and their vulnerability to disease leading to blindness. GCs in particular are lost to neurodegenerative disorders such as glaucoma, Alzheimer?s disease, Parkinson?s disease, and multiple sclerosis. We also know from histology that a small fraction of these cells die each year as part of the normal aging process. Unfortunately, techniques to assess population loss and general health of GCs and other inner retinal neurons in vivo are limited. New optical modalities that are rapid, specific, and non-invasive promise to greatly enhance our ability to monitor the spatial and temporal dynamics of inner retinal neurons. This study takes advantage of unique optical instrumentation developed in my laboratory that combines adaptive optics and optical coherence tomography to achieve cellular-level 3D imaging of the living human retina. We will use this technique to investigate three specific aims that quantify the spatial properties of inner retinal neurons and their change in aging and glaucoma. The long term goal of this research is to establish high resolution, high specificity optical techniques as valid tools for probing structure and physiologic processes of the retina at the cellular scale. The resulting ability to study cells in vivo will improve early detection of and treatment monitoring for diseases that impact the retina.

Public Health Relevance

This study takes advantage of unique camera technology developed in my laboratory for live imaging of transparent neurons in the human retina, capturing exquisite cellular details in 3D. We will use this camera to investigate early changes that occur in these transparent neurons caused by aging and glaucoma. Results of this study may help improve our ability to detect earlier and monitor treatment more accurately some of the most blinding diseases in the world.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
1R01EY029808-01
Application #
9642056
Study Section
Diseases and Pathophysiology of the Visual System Study Section (DPVS)
Program Officer
Greenwell, Thomas
Project Start
2019-04-01
Project End
2023-03-31
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Indiana University Bloomington
Department
Type
Schools of Optometry/Opht Tech
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401