Retinal remodeling This renewal is based on our discovery that retinal degenerations are two separate diseases. Acute primary photoreceptor degenerations turn into chronic neurodegenerations mimicking brain diseases called ?pro- teinopathies?. The neurodegeneration is unremitting, slowly destroying the neural retina with > 90% loss of retinal neurons, severely impeding rescue. The proposal aims to pro?le proteinopathy molecules; identify net- works underlying metabolic collapse; map the nature and scope of rewiring and neuronal loss, and develop a pigmented Tg P347L rabbit model of human adRP.
Aim 1. Pro?le neurodegenerative proteinopathy molecules in the neurodegenerative retina. Hypothesis. Retinal neurodegeneration is a proteinopathy. Outcomes: A comprehensive, proteinopathy ?nger- print spanning 6y of disease progression. Signi?cance. Interventions for blinding diseases require survival of the retina. Neurodegeneration must be overcome.
Aim 2. Characterize of the metabolic / signaling collapse of the ND retina. Hypothesis. ND corrupts neuronal signaling and energetics. Outcomes: Metabolome status for all neurons and glial cells spanning 6y of ND. Signi?cance. If neurodegenerative retinas cannot sustain activity, therapeutic in- terventions are destined to fail. Metabolic network mapping may reveal druggable targets.
Aim 3. Develop a pathoconnectome spanning mid and late ND. Hypothesis. Neural rewiring in the retina is driven by interactions between survivor and degenerating neurons. Outcomes. The survivorship and connectivity of the ND retina. Signi?cance. Different rescue schemas have different targets and the status of each is critical.
Aim 4. Develop a pigmented Tg P347L rabbit for retinal degeneration research. Hypothesis. A pigmented eye is optimal for studying of retinal degenerations. Outcomes. A long lifespan, eco- nomically viable, large-eye pigmented model suitable for the FDA Animal Model Quali?cation Program, imag- ing, and analysis of disease progression, rescue and ND interventions. Signi?cance. Developing therapies for human retinal disorders will eventually have to proceed beyond mouse models. A pigmented rabbit is an ideal platform for intervention testing.

Public Health Relevance

This project is based on the discovery that retinal degenerations are binary diseases: acute photore- ceptor degenerations convert to chronic neurodegenerations similar to progressive brain diseases called ?proteinopathies?. The goals are to diagnose the proteinopathy and its associated metabolic im- pairments. Treating these defects are critical to achieving rescues vision rescue by molecular, cellular, or engineering approaches.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY015128-13
Application #
9453704
Study Section
Diseases and Pathophysiology of the Visual System Study Section (DPVS)
Program Officer
Greenwell, Thomas
Project Start
2004-08-01
Project End
2022-03-31
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
13
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Utah
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
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Nagarajan, N; Jones, B W; West, P J et al. (2018) Corticostriatal circuit defects in Hoxb8 mutant mice. Mol Psychiatry 23:1-10
Loizos, Kyle; Marc, Robert; Humayun, Mark et al. (2018) Increasing Electrical Stimulation Efficacy in Degenerated Retina: Stimulus Waveform Design in a Multiscale Computational Model. IEEE Trans Neural Syst Rehabil Eng 26:1111-1120
Nagarajan, N; Jones, B W; West, P J et al. (2017) Corticostriatal circuit defects in Hoxb8 mutant mice. Mol Psychiatry :
Yoshioka, Nayuta; Zangerl, Barbara; Nivison-Smith, Lisa et al. (2017) Pattern Recognition Analysis of Age-Related Retinal Ganglion Cell Signatures in the Human Eye. Invest Ophthalmol Vis Sci 58:3086-3099
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Wahlin, Karl J; Maruotti, Julien A; Sripathi, Srinivasa R et al. (2017) Photoreceptor Outer Segment-like Structures in Long-Term 3D Retinas from Human Pluripotent Stem Cells. Sci Rep 7:766
Foster, James W; Wahlin, Karl; Adams, Sheila M et al. (2017) Cornea organoids from human induced pluripotent stem cells. Sci Rep 7:41286
Phu, Jack; Khuu, Sieu K; Nivison-Smith, Lisa et al. (2017) Pattern Recognition Analysis Reveals Unique Contrast Sensitivity Isocontours Using Static Perimetry Thresholds Across the Visual Field. Invest Ophthalmol Vis Sci 58:4863-4876
Pfeiffer, Rebecca L; Marc, Robert E; Kondo, Mineo et al. (2016) Müller cell metabolic chaos during retinal degeneration. Exp Eye Res 150:62-70

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