The visual system exhibits a heightened sensitivity to the quality visual experience during an interval late in development termed the `critical period'. Discordant vision during the critical period is the cause of amblyopia, a prevalent visual disorder in children. Treatment of amblyopia is most effective in children before the close of the critical period. Subsequently, the flexibility with brain circuitry diminishes in adulthood and effective therapy is more difficult. In a mouse model of amblyopia, disrupting normal vision by closing one (monocular deprivation, MD) for the duration of the critical period, but not thereafter, decreases visual acuity and perturbs the normal eye dominance of neurons in visual cortex. The nogo-66 receptor gene (ngr1) is required to close the critical period. In ngr1 mutant mice, plasticity during the critical period is normal, but it is retained in adult mice. Importantly, ngr1 mutant mice spontaneously recover visual acuity in this model of amblyopia. Our overall hypothesis is that recovery of acuity and eye dominance are independent. In the proposed research, we take advantage of this extended critical period in ngr1 mice to identify with location and mechanisms of plasticity that mediate recovery of acuity and eye dominance with a combination of conditional mouse genetics, behavioural assays, electrophysiology, sophisticated repeated in vivo calcium imaging and laser-scanning photostimulation circuit mapping. We will begin to unravel how plasticity within visual circuitry mediates recovery of visual function following early abnormal vision (MD), as well as how this plasticity is restricted to the critical period with these experiments. In addition to improving understanding of how experience-dependent plasticity changes the function of brain circuits, these studies may reveal new avenues for developing therapeutic approaches to treat amblyopia. .

Public Health Relevance

Abnormal vision only during a ?critical period? in childhood induces amblyopia, also known as lazy eye, a disorder comprising several deficits in spatial vision including poor acuity. The proposed research is relevant to public health because knowledge of the neural circuits that mediate recovery of acuity and eye dominance will improve our understanding of targets for therapeutic intervention. Thus, the proposed research is relevant to the mission of the both the NEI to increase understanding of the critical period in order to determine how experience alters connectivity in the developing visual system.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY021580-08
Application #
9754152
Study Section
Mechanisms of Sensory, Perceptual, and Cognitive Processes Study Section (SPC)
Program Officer
Greenwell, Thomas
Project Start
2012-05-01
Project End
2021-07-31
Budget Start
2019-08-01
Budget End
2020-07-31
Support Year
8
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Louisville
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
057588857
City
Louisville
State
KY
Country
United States
Zip Code
40292
Stephany, Céleste-Élise; Ma, Xiaokuang; Dorton, Hilary M et al. (2018) Distinct Circuits for Recovery of Eye Dominance and Acuity in Murine Amblyopia. Curr Biol 28:1914-1923.e5
Frantz, Michael G; Kast, Ryan J; Dorton, Hilary M et al. (2016) Nogo Receptor 1 Limits Ocular Dominance Plasticity but not Turnover of Axonal Boutons in a Model of Amblyopia. Cereb Cortex 26:1975-85
Stephany, Céleste-Élise; Ikrar, Taruna; Nguyen, Collins et al. (2016) Nogo Receptor 1 Confines a Disinhibitory Microcircuit to the Critical Period in Visual Cortex. J Neurosci 36:11006-11012
Stephany, Céleste-Élise; Frantz, Michael G; McGee, Aaron W (2016) Multiple Roles for Nogo Receptor 1 in Visual System Plasticity. Neuroscientist 22:653-666
Stephany, Céleste-Élise; Chan, Leanne L H; Parivash, Sherveen N et al. (2014) Plasticity of binocularity and visual acuity are differentially limited by nogo receptor. J Neurosci 34:11631-40
Priebe, Nicholas J; McGee, Aaron W (2014) Mouse vision as a gateway for understanding how experience shapes neural circuits. Front Neural Circuits 8:123
Park, Jennifer I; Frantz, Michael G; Kast, Ryan J et al. (2014) Nogo receptor 1 limits tactile task performance independent of basal anatomical plasticity. PLoS One 9:e112678