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We produced 8 lines of transgenic (Tg) rats expressing one of two different rhodopsin mutations in albino Sprague-Dawley (SD) rats. Three lines were generated with a proline to histidine substitution at codon 23 (P23H), the most common autosomal dominant form of retinitis pigmentosa in the United States. Five lines were generated with a termination codon at position 334 (S334ter), resulting in a C-terminal truncated opsin protein lacking the last 15 amino acid residues and containing all of the phosphorylation sites involved in rhodopsin deactivation, as well as the terminal QVAPA residues important for rhodopsin deactivation and trafficking. The rates of photoreceptor (PR) degeneration in these models vary in proportion to the ratio of mutant to wild-type rhodopsin. The models have been widely studied, but many aspects of their phenotypes have not been described. Here we present a comprehensive study of the 8 Tg lines, including the time course of PR degeneration from the onset to one year of age, retinal structure by light and electron microscopy (EM), hemispheric asymmetry and gradients of rod and cone degeneration, rhodopsin content, gene dosage effect, rapid activation and invasion of the outer retina by presumptive microglia, rod outer segment disc shedding and phagocytosis by the retinal pigmented epithelium (RPE), and retinal function by the electroretinogram (ERG). The biphasic nature of PR cell death was noted, as was the lack of an injury-induced protective response in the rat models. EM analysis revealed the accumulation of submicron vesicular structures in the interphotoreceptor space during the peak period of PR outer segment degeneration in the S334ter lines. This is likely due to the elimination of the trafficking consensus domain as seen before as with other rhodopsin mutants lacking the C-terminal QVAPA. The 8 rhodopsin Tg lines have been, and will continue to be, extremely useful models for the experimental study of inherited retinal degenerations., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

RDS (retinal degeneration slow) is a photoreceptor-specific tetraspanin protein required for the biogenesis and maintenance of rod and cone outer segments. Mutations in the Rds gene are associated with multiple forms of rod- and cone-dominant retinal degeneration. To gain more insight into the mechanisms underlying the regulation of this gene, the identification of regulatory sequences within the promoter of Rds was undertaken. A 3.5 kb fragment of the 5' flanking region of the mouse Rds gene was isolated and binding sites for Crx, Otx2, Nr2e3, RXR family members, Mef2C, Esrrb, NF1, AP1, and SP1 in addition to several E-boxes, GC-boxes and GAGA-boxes were identified. Crx binding sequences were conserved in all mammalian species examined. Truncation expression analysis of the Rds promoter region in Y-79 retinoblastoma cells showed maximal activity in the 350 bp proximal promoter region. We also show that inclusion of more distal fragments reduced promoter activity to the basal level, and that the promoter activities are cell-type and direction specific. Co-transfection with Nrl increased promoter activity, suggesting that this gene positively regulates Rds expression. Based on these findings, a relatively small fragment of the Rds promoter may be useful in future gene transfer studies to drive gene expression in photoreceptors., (Copyright 2010 Elsevier Ltd. All rights reserved.)

To examine its potential role within the retina as a modulator of cell death and photoreceptor degeneration, bcl-2 expression was targeted to the photoreceptors of transgenic mice by the human IRBP promoter. Three transgenic families were established, with levels of transgene expression between 0.2 and two-fold relative to that of endogenous bcl-2. The effect of bcl-2 expression on genetically programmed photoreceptor degeneration was evaluated by crossing these transgenic mice with mice that develop a rapid degeneration of rod photoreceptors due to expression of a distinct transgene, SV40 T antigen (Tag). Transgenic Bcl-2 was localized to photoreceptor inner segments and was capable of abrogating the activation of caspase activity and the resulting cell death associated with ectopic expression of Tag. However, Bcl-2 itself ultimately caused photoreceptor cell death and retinal degeneration. Several proteins not expressed normally in Tag or other transgenic retinas undergoing photoreceptor degeneration were induced in the Bcl-2 transgenic retinas. Analysis by mass spectroscopy identified one of these proteins as alphaA-crystallin, a member of a protein family that associates with cellular stress. Since Bcl-2 can promote as well as spare cell death in the same photoreceptor population, its potential utility in ameliorating photoreceptor death in human hereditary blinding disorders is compromised., ((C) 2001 Academic Press.)

We have recently noted that the inner nuclear layer (INL) and the inner plexiform layer (IPL) were significantly thinner in mice homozygous for the nervous defect (nr / nr) than in control (nr /+ or +/+) littermates. Here, we have carried out a series of anatomical studies to further understand these inner retinal changes. At postnatal day (P) 13, there was no difference in the inner retina between nervous and control mice, while a significant difference was observed at P30. Similar changes were not seen in other mouse models of photoreceptor degeneration. There was a significant reduction in the density of cells in the INL that were stained by antibodies against the inhibitory neurotransmitters GABA and glycine. These results indicate that the nervous defect causes a degeneration of one or more sub-types of amacrine cells, in addition to the loss of cerebellar Purkinje cells and retinal photoreceptors that is known to occur in these mutant animals. Finally, evidence is provided that photoreceptors die by an apoptotic pathway in nervous mice., (Copyright 2001 Academic Press.)

Albino rats were born and raised in one of three cyclic (12L: 12D) lighting conditions: (1) 5 lux for 9 weeks, (2) 800 lux for 9 weeks, or (3) 800 lux for 9 weeks, followed by 5 lux for 3 weeks (800:5). After the treatment, the following were determined: (i) retinal function as measured by the electroretinogram (ERG); (ii) retinal morphology, including rod outer segment (ROS) length and outer nuclear layer area; (iii) rhodopsin levels in whole retina and ROS preparations; (iv) fatty acid profile of ROS membranes and (v) retinal antioxidant levels. After 9 weeks, rats raised in 800 lux sustained an irreversible loss of photoreceptors which could not be reversed by then placing them in 5 lux. However, these rats displayed significant alterations in all other parameters measured after the 3 weeks in dim cyclic light. ERGs showed a 60% increase of b-wave maximum amplitude in 800:5 rats at 12 weeks over the value at the time of their change to a dim environment, while a-wave amplitude in 800:5 rats increased more than 2.5 times. This increase can be explained by a combination of increased ROS length and increased ROS membrane concentration of rhodopsin during the three weeks in 5 lux. Polyunsaturated fatty acids predominated in the ROS of 5 lux rats and 800:5 rats, but not in 800 lux animals. Measurements of retinal glutathione enzyme activity and vitamin E and C levels were relatively low in 800:5 rats. Some rats from the 800:5 group were exposed to 2000 lux for 24 hr. Retinas of these rats sustained 50% loss of photoreceptors from this exposure. Comparisons are made to previous studies concerning the effect of cyclic light environments on the retinas of albino rats.

We have compared the specific activities of glutathione-dependent enzymes in rod outer segments (ROS) and in whole retina of rabbits and rats, using three different assays. In the first, glutathione peroxidase (GSH-Px) activity was measured as the combined activities of the Se-dependent and Se-independent forms using cumene hydroxide as a substrate. In the second, Se-dependent GSH-Px alone was measured using hydrogen peroxide (H2O2) as a substrate. In the third, the combined activities of several enzymes, collectively known as GSH-S-transferase, were measured. The latter includes the activity of the Se-independent GSH-Px. GSH-Px activity (Se-dependent and Se-independent combined) in ROS of rat and rabbit were found to be 47.7 +/- 8.2 and 72.9 +/- 11.9 nmol of GSH oxidized min-1 mg-1 soluble protein, respectively. From whole retina, values were 67.3 +/- 6.0 and 128.8 +/- 12.3, respectively. Se-dependent GSH-Px specific activities from the above tissues were 43.5 +/- 2.9 (rat ROS). 70.6 +/- 11.3 (rabbit ROS), 30.6 +/- 9.6 (rat whole retina), and 113.2 +/- 12.2 (rabbit whole retina). GSH-S-transferase activity was negligible in rabbit ROS, whereas, in rat ROS, it was 40.4 +/- 8.0, expressed as nmol of S-2,4-dinitrophenylglutathione produced min-1 mg-1 soluble protein. In contrast, the GSH-S-transferase specific activity in whole rabbit retinas was about eight times that found in the rat retina (101.5 +/- 12.3 for rat retina and 885.3 +/- 60.0 for rabbit retina). These results demonstrate that ROS contain glutathione enzymes which are important in protecting membranes from oxidative stresses by reducing hydrogen peroxide and lipid hydroperoxides at the site of their formation.

Albino rats were born and raised to 12 weeks of age in 12L:12D light regimes of 5, 300 or 800 lx. Upon killing, the activities of the following glutathione enzymes were measured in the neuroretina: (1) glutathione peroxidase; (2) glutathione-S-transferase; and (3) glutathione reductase. Also measured were vitamin E, ascorbic acid, and the levels of oxidized and reduced glutathione. Animals raised in 800-lx cyclic light have a significant increase in the retinal activities of the three glutathione enzymes over activities measured in animals raised in the two dimmer regimes. The retinal level of vitamin E, measured per nmol of lipid phosphorus, is directly and significantly correlated with rearing illuminance (P less than 0.05). The same is true of retinal ascorbic acid, which shows a 30% increase in the 800-lx-reared rats over the level of those raised in the intermediate light regime (300 lx). Some of the animals from each group were exposed to 2000 lx for 24 hr to determine if correlations existed between the levels of retinal antioxidants listed above and susceptibility to light damage. Animals raised in 5-lx cyclic light lost almost all of their photoreceptors as a result of the exposure. Rats raised in 300-lx cyclic light lost a small but significant number (ca. 20%), while those raised in 800 lx sustained no light damage. Electroretinographic evaluation supports these morphometrical findings.