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Nrl-Knockout Mice Deficient in Rpe65 Fail to Synthesize 11-cis Retinal and Cone Outer Segments

¹From the Departments of Ophthalmology and Visual Sciences, ⁶Human Genetics, and ⁷Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan; the ³Department of Ophthalmology, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; and the ⁴Departments of Pharmacology and ⁵Neurosciences, University of California-San Diego, La Jolla, California.

PURPOSE. To define rod and cone function further in terms of visual cycle mechanism, the retinal phenotype resulting from Rpe65 (retinoid isomerase I) deficiency in Nrl^–/– mice having a single class of photoreceptors resembling wild-type cones was characterized and outcomes of retinoid supplementation evaluated.

METHODS. Rpe65^–/–/Nrl^–/– mice were generated by breeding Rpe65^–/– and Nrl^–/– strains. Retinal histology, protein expression, retinoid content, and electroretinographic (ERG) responses were evaluated before and after treatment with 11-cis retinal by intraperitoneal injection.

Results

Retinas of young Rpe65^–/–/Nrl^–/– mice exhibited normal lamination, but lacked intact photoreceptor outer segments at all ages examined. Rpe65, Nrl, and rhodopsin were not detected, and S-opsin and M/L-opsin levels were reduced. Retinyl esters were the only retinoids present. In contrast, Nrl^–/– mice exhibited decreased levels of retinaldehydes and retinyl esters, and elevated levels of retinols. ERG responses were elicited from Rpe65^–/–/Nrl^–/– mice only at the two highest intensities over a 4-log-unit range. Significant retinal thinning and outer nuclear layer loss occurred in Rpe65^–/–/Nrl^–/– mice with aging. Administration of exogenous 11-cis retinal did not rescue retinal morphology or markedly improve ERG responses.

CONCLUSIONS. The findings provide clarification of reported cone loss of function in Rpe65^–/–/Nrl^–/– mice, now showing that chromophore absence results in destabilized cone outer segments and rapid retinal degeneration. The data support the view that rod-dominant retinas do not have a cone-specific mechanism for 11-cis retinal synthesis and have potential significance for therapeutic strategies for rescue of cone-rich retinal regions affected by disease in the aging human population.

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