Thursday, May 2, 2024
5/2/2024
Abstract Retinitis pigmentosa (RP) is the most common group of inherited retinal disorders associated with progressive loss of vision. RP is typically diagnosed in adulthood following the onset of night blindness and impaired peripheral vision. Longitudinal studies of patients with RP reveal that their loss of visual acuity is significantly slower than the deterioration of their photoreceptor function. How the visual system sustains acuity despite the progressive loss of photoreceptors is unclear. Our hypothesis is that flexibility within the circuits of the visual system engage with the progressive loss of visual output to impair acuity. We will test our hypothesis by first characterizing the deficit in acuity and related functional characteristics in visual cortex and retina in using the rhodopsin P23H/+ (rho P23H/+) mutant mouse model. These mice have similar declines in retinal function and are a good model of human RP. Then we will evaluate whether enhancing or reducing experience-dependent plasticity affects the trajectory of the progressive loss of vision of rho P23H/+ mice by then characterizing the deficit in acuity and related functional characteristics in visual cortex and retina in using the rhodopsin P23H/+ (rho P23H/+) mutant mice that also lack a gene that limits plasticity in adult visual circuitry (nogo-66 receptor, ngr1) or that is required for visual plasticity (activity-regulated cytoskeleton-associated protein, ARC). Mice lacking ngr1 (ngr1 -/-) display greater visual plasticity than adult wild-type mice while mice lacking ARC (ARC -/-) exhibit reduced visual plasticity.
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