Conditioned medium-mediated photoreceptor differentiation in retina from embryonic rd chickens.

Retina cells from 8-day rd (retinal degenerate) chicken embryos were cultured in media supplemented with optic lobe conditioned medium (OLCM). The morphogenesis of rd photoreceptors is being described. Several differentiating photoreceptors depicted a membranous sac protruding from the apical end of the cell as revealed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Such structures were found mostly in 8-day-old cultures supplemented with OLCM and were absent in controls. They resembled rudimentary outer segments emanating from a cilium at the apical inner segments. TEM showed a few stacks of free floating disks within the membranous structure which was suggestive of a rudimentary outer segment development. The possible neurotrophic effect of OLCM on rd retina photoreceptor differentiation is being suggested.

Radioimmunocytochemical localization of retinal S-antigen with monoclonal antibodies.

Two monoclonal antibodies (RSA1/83 and RSA2/83) were developed against a homogeneous preparation of bovine retinal S-antigen. The two hybridomas produced by mouse X mouse hybrid myeloma cells secrete immunoglobulin G. Indirect autoradiography on glutaraldehyde-fixed preparations of bovine explants was used to locate the antigenic site. Antibody RSA1/83 recognizes the antigen primarily in the apical region of the rod outer segment, while antibody RSA2/83 located the antigen both in the outer and inner segments of the rod photoreceptor cells. A distinct band of silver grains also appeared along the inner limiting membrane with both antibodies. Control explants showed no specific labeling pattern over the various retinal compartments.

Tunicamycin-induced dysgenesis of retinal rod outer segment membranes. I. A scanning electron microscopy study.

Incubation of Xenopus retinas with tunicamycin has been shown to block the glycosylation of opsin, the rod visual pigment apoglycoprotein, with concomitant accumulation of vesicular membrane material in the compartment between the rod inner and outer segments (i.e., the intersegmental space) (Fliesler et al, J Cell Biol 100:574-587, 1985). To further assess the morphology, topology, and cellular origin of this membranous material, Xenopus retinas were incubated in the presence or absence of tunicamycin and the photoreceptor cells were examined by scanning electron microscopy. The material which accumulated in the intersegmental space appeared to be a complex of membranous structures consisting of cisternae with numerous tubular projections, as well as closely associated individual vesicles of various sizes. This tubulo-vesicular material was exclusively associated with the basal surface of the rod outer segment. The connecting cilium, periciliary ridge complex, and the apical surface of the rod inner segment were devoid of such membrane material. Nascent (open) discs (i.e., evaginations of the plasma membrane at the base of the outer segment) often observed in control retinas were not present in tunicamycin-treated tissue. These results support the hypothesis that the membranous material which accumulates in the intersegmental space of rods in tunicamycin-treated retinas represents incompletely and aberrantly formed nascent disc membranes. The formation of this material is apparently a consequence of a deficiency in newly synthesized, asparagine-linked membrane glycoconjugates (e.g., the oligosaccharide chains of opsin) at the site of disc assembly.

Sensitivity of photoreceptors to elevated levels of cGMP in the human retina.

When isolated human retinas were cultured in the presence of a phosphodiesterase inhibitor or dibutyryl cyclic guanosine monophosphate (dbcGMP), degenerative changes occurred which were proportional to the concentration of drug used and the period of exposure. Low concentrations of either drug did not alter retinal morphology as compared to controls. Higher concentrations provoked vesiculation of rod inner segments and rounding up of cones. Numerous pyknotic nuclei were noted in the outer nuclear layer of those preparations. Combining IBMX and dbcGMP in the same medium destroyed virtually every rod in the specimen within 8 hr of incubation. Under those conditions, cones remained structurally intact although somewhat rounded. In all treatments, cells of the innerretinal layers maintained normal morphology. Our results suggest that elevated levels of cGMP in the human retina can alter certain metabolic processes in photoreceptors, which leads to degenerative changes and cell death uniquely in rod photoreceptors.

Scanning electron microscopy of human drusen.

Drusen are small, yellowish deposits that form under the retinal pigment epithelium (RPE) with senescence or under certain pathological conditions. The present study examined these structures under the scanning electron microscope. Tissue came from four eyes of 66- and 75-year-old donors who demonstrated widespread drusen of the posterior fundus noted on postmortem examination. Specimens were prepared by either detaching the RPE from Bruch's membrane, or by cryofracturing the tissue for cross-sectional views. Drusen appeared to be composed of irregularly-shaped globular masses and of distinct spherical entities. These particles varied greatly in size, and were situated between the RPE's basement membrane and the outer collagenous zone of Bruch's membrane. Surface views showed drusen components to be embedded in the collagenous zone of Bruch's membrane. Pits corresponding to the sizes of the globular and spherical masses imply that some particles were lost during tissue processing. Fractured cross sections of the irregularly-shaped globular masses revealed a homogeneous, granular matrix with no distinct ultrastructural features, while some of the fractured spherical components demonstrated an internal core. Transmission electron microscopic analysis on the same specimens that were subjected to SEM corroborated these observations. Analytical x-ray microanalysis (Kevex, Foster City, CA) in the SEM revealed major peaks for calcium and phosphorous in the crystalline spherical components, and primarily potassium and chloride in the globular structures.

Rhodopsin, vitamin A, and interstitial retinol-binding protein in the rd chicken.

In order to determine whether blindness in the rd strain of Rhode Island Red chickens is due to a defect in the vitamin A (visual) cycle, spectroscopy, high performance liquid chromatography, and immunochemical techniques were used to compare the amounts of rhodopsin, interstitial retinol-binding protein, and vitamin A compounds in the dark-adapted eyes of homozygous rd and heterozygous carriers. In both groups of chickens, (up to 6 weeks post-hatching) the distribution of stored vitamin A differed from other vertebrates (mammals, amphibians, fish) in that more than half of the retinyl palmitate/stearate occurred in the neurosensory retina. The 11-cis isomer accounted for nearly 100% of the retinyl palmitate/stearate in the neurosensory retinas of both groups. In the pigmented layers (pigment epithelium and choroid) the 11-cis isomer amounted to 70.1 +/- 4.2% in the carrier, and 65.1 +/- 2.9% in the rd birds. With respect to their content of rhodopsin, IRBP, retinyl palmitate/stearate and unesterified retinol, (both 11-cis and all-trans isomers) no significant difference could be demonstrated between the eyes of rd and carrier chickens (3 days and 28 days post-hatching). These results therefore demonstrate that the ocular tissues of rd chickens do not lack IRBP, the putative extracellular transport protein for vitamin A, that these tissues synthesize and store the 11-cis isomer of vitamin A, and that the 11-cis isomer is used to form rhodopsin.(ABSTRACT TRUNCATED AT 250 WORDS)

Distributions of elements in the human retinal pigment epithelium.

Distributions of elements above the atomic number of sodium were mapped in the retinal pigment epithelia of eight human eyes. X-ray energy spectra and maps were collected from cryofixed, freeze-dried, and epoxy-embedded tissues using energy-dispersive x-ray microanalysis. All eyes had high concentrations of phosphorus in the nuclei of retinal pigment epithelial cells. Melanosomes were rich in sulfur, zinc, calcium, and iron. Lipofuscin and cytoplasm contained only phosphorus and sulfur in detectable amounts. Drusen, when present, contained phosphorus and calcium. Six eyes had a prominent aluminum peak recorded from melanosomes, nuclei, and Bruch's membrane. In one pair of 90-year-old eyes, small, electron-dense deposits surrounded many melanosomes and contained mercury and selenium. Retinal pigment epithelial melanosomes may bind and accumulate metals and other potentially toxic ions over time, preventing them from reaching the neural retina.

Excitatory amino acid involvement in retinal degeneration.

Amino acid analysis using high-performance liquid chromatography demonstrated high levels of the excitatory amino acids, aspartate and glutamate, in the retinas of congenitally blind chicks at the time of photoreceptor degeneration. Concentrations of aspartate were about 2 times higher in blind chicks than in retinas of age-matched sighted chicks that were carriers for the genetic defect. Glutamate levels were similar in blind chicks and carriers at 1 day of age, but doubled and tripled sighted chick values at 1 week and 2 weeks of age in blind chick retinas. Light microscopic immunocytochemistry using antibodies that recognize aspartate and glutamate revealed increased levels of these two amino acids specifically in the photoreceptor layer of blind chicks. This report is the first to demonstrate high endogenous levels of excitatory amino acids associated with a hereditary degeneration of photoreceptor cells.

A primate model for age related macular drusen.

A closed colony of semi-free-ranging rhesus monkeys maintained in isolation since 1938 by the Caribbean Primate Research Center (CPRC) is being studied as a model for age related macular drusen. Of examined colony animals 57.7% of the monkeys and 47.3% of their eyes have drusen. The prevalence and severity of drusen are linearly related to increasing age and are significantly higher in specific maternal lineages (matrilines). An electrophysiological estimate indicates loss of function associated with drusen. Prevalence of drusen in CPRC females is almost twice that of males, while the prevalence among CPRC animals in general appears to be several times that of monkeys from continental US facilities. Evidence suggests that the frequency of endstage lesions is also similar to that in human populations. The CPRC matriline monkeys appear to provide the best model yet reported for human age related macular drusen.

Cell death and optic fiber penetration in the optic stalk of the chick.

The role of dying cells in the optic stalk in relation to retinal fiber migration was investigated in the chick embryo. Cell death was analysed at various stages of development by counting pycnotic nuclei and also by the Gomori acid phosphatase reaction, while nerve fibers were visualised by the Bodian method. A wave of cell death, beginning in the neural retina at stage 18 and advancing with time through the stalk towards the diencephalon, occurred simultaneously or slightly prior to differentiation and migration of ganglion cell axons. Cell death stopped and gliogenesis occurred in the stalk after penetration by retinal fibers. Cell death occurred in the stalk even when fiber penetration was prevented by optic cup ablation. In this case, necrosis ensued until almost complete degeneration of the stalk, usually within three days after the operation, and gliogenesis did not occur. As the stalk degenerated, its cells became heavily pigmented. These observations suggest that the onset of cell death in the optic stalk is determined prior to and independently of retinal fiber penetration. On the other hand, cessation of cell death and subsequent gliogenesis occur only in the presence of ingrowing optic fibers.

An SEM AND TEM study of suppression of eye development in eyeless mutant axolotls.

Morphology of the primary optic rudiment of normal eyed and mutant eyeless (e/e) axolotl embryos was studied at light. Tem and SEM levels. The presumptive eyeforming region of eyeless embryos differs from that of normal embryos in several important respects including premature formation of basal lamina, separation from overlying ectoderm by mesenchyme cells and persistence of granules in the interspace surrounding the optic anlage into relatively late developmental stages. These differences suggest that the gene that causes failure of eye formation in the mutant axolotls produces structural differences that interfer with normal physical and/or biochemical inductive interactions between neurectoderm and mesenchyme cells due primarily to the precocious development of basal lamina over the extermal surface of the optic primordia.

Ultrastructural changes in the retinal pigment epithelium of congenitally blind chickens.

Pathological changes in the retinal pigment epithelium (RPE) in a strain of chickens having hereditary blindness and retinal degeneration were described at the ultrastructural level. Photoreceptors in the retinal degenerate (rd) chicken had previously been noted to degenerate within a week after hatching. Affected chicks have neural retinas that are morphologically comparable to normal animals prior to that time despite an obvious lack of vision. In the present study, no pathological changes were noted in rd RPE prior to the time of photoreceptor degeneration. However, while mitochondria in the normal chick's RPE underwent diurnal changes in morphology within a few days of hatching, pleomorphic or ring mitochondria were not seen with high frequency in the rd chick. After photoreceptors began degenerating, changes were seen in the rd RPE. By 2 weeks of age, we noted a reduction in the depth and number of basal infoldings, an increase in number and size of autophagic vacuoles and large whorls of membranous material within rd RPE cells. Membranous debris and what appeared to be broken off outer segments were seen in the subretinal space at that time. These phenomena became more prominent and prevalent with time. In 3-4 week old specimens, nearly intact outer segments were seen within RPE cytoplasm. At the same time very few intact outer segments were present on photoreceptors. After this time degenerative changes were seen in the RPE: a thinning of cells (apical to basal cell width), spreading out of cells (increased distance between intercellular junctional complexes), hypopigmentation of cells and presence of free cells in the sub-retinal space. Some RPE cells appeared in a rounded up configuration, bulging into the subretinal space and making junctional complexes with remaining photoreceptor inner segments or Mueller cell processes. Many RPE cells did appear to maintain their phagocytic abilities, as evidenced by presence of many microvilli and pinocytotic vacuoles in the apical cytoplasm.

Axonal transport and central visual projections of ganglion cells in congenitally blind chickens.

The rd (retinal degenerate) strain of chicken is an example of a recessively inherited mutation characterized by blindness at the time of hatching, as defined by behavioral and electrophysiological tests. Paradoxically, blind mutants have normal retinal morphology, even at the ultrastructural level. Eventually, however, the entire retina degenerates in this strain, perhaps as a result of disuse atrophy. Results of preliminary studies imply that a defect in the visual transduction cascade in photoreceptor cells is responsible for the lack of vision. As well as being an important animal model for studies on photochemistry and transduction, the rd chicken may afford a paradigm for studies on inner retinal physiology and pathology, as electrical input to this inner neuronal system appears to be absent. In the current study we examined axonal transport (both retrograde and anterograde) in rd retinal ganglion cells and connectivity of ganglion cells to visual centers in the brain and compared these to normally sighted chicks. All visuorecipient nuclei were present in rd animals and appeared normal at the light microscopic level. When 3H-proline was injected into one eye of a blind chicken on the day of hatching, labeled polypeptides or proteins were transported via a fast transport mechanism to the same visual centers in roughly the same quantities as in normally sighted chicks. When horseradish peroxidase (HRP) was injected in the optic tectum of blind and normal 1 day old chicks, this label was transported retrogradely to the soma of retinal ganglion cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Differential sensitivity of protein synthesis in human retina to a phosphodiesterase inhibitor and cyclic nucleotides.

When human retinas are cultured in the presence of various phosphodiesterase (PDE) inhibitors or cyclic nucleotide analogues, rod photoreceptors undergo degenerative changes followed by cell death within 8 hours of incubation, whereas cone photoreceptors and other retinal cells are affected minimally. In the present study we found that the PDE inhibitor, isobutylmethylxanthine (IBMX), as well as the dibutyryl analogues of cGMP and cAMP, inhibited protein synthesis in short-term cultures of human retinas under conditions where uptake of exogenously supplied 3H-leucine was not diminished (relative to controls). The results of an autoradiographic analysis suggested that inhibition of protein synthesis by these drugs occurred to a greater extent in rod photoreceptors than in cones or other retinal cells, and that this phenomenon happened prior to the onset of any morphological changes. When retinas incubated in IBMX for 4 hours were returned to control medium for an additional incubation, rods recovered their ability to synthesize proteins and cell viability was maintained. The results of polyacrylamide gel electrophoresis indicated that IBMX caused a general inhibition of retinal protein synthesis rather than affecting the synthesis of specific retinal proteins. These observations are discussed with regard to possible mechanisms underlying rod-specific photoreceptor degeneration.

Adult-onset macular degeneration in the Cayo Santiago macaques.

Since 1985 a group from the University of Florida has examined 136 rhesus monkeys from the Cayo Santiago colony. From the sample, 97 are older than nine years (approximately 30 human years) and 39 are younger. Drusen were found in 17% of the younger eyes and in 46% of the older eyes. All animals over 25 years of age had drusen in the central fundus. The incidence of drusen varied from 19-77% between five social groups. Incidence reported in random-source colonies in the continental U.S.A. is about six percent. Compared to near-age matched controls without drusen, selected rhesus exhibited visual resolution losses amounting to two Snellen-lines or more. The end-stage disciform changes and ultrastructural similarities are comparable with human macular disease. Future prospective studies may include therapies, surgical intervention, environmental manipulation and genetic research.

Scanning electron microscopy of the retina in an animal model of hereditary blindness.

Scanning electron microscopy was performed on retinas from normal and a mutant strain of chickens suffering from congenital blindness with retinal degeneration. Both surface and cryofractured transverse views of the retina were examined. Photoreceptors were generally seen to degenerate along a central to peripheral gradient: the more damaged receptors located centrally while areas of normal appearing photoreceptors were located toward the ora serrata. Pathological changes included deformed and missing outer segments and short, swollen inner segments. Reactive changes in overlying pigment epithelium (PE) were also noted over areas displaying advanced photoreceptor degeneration. PE changes included both hypertrophy and dystrophy of cells, detached cells, and formation of clusters or nodules along Bruch's membrane or in the sub-retinal space among photoreceptor inner segments. Among the 6 types of photoreceptors in the chicken retina (1 type of rod and 5 types of cones), more intact double cones were identified in areas undergoing retinal degeneration than other types. Double cones may be more resistant to the factor(s) involved in cellular death.

Hereditary retinal degeneration in the Rhode Island Red chicken: ultrastructural analysis.

An electron microscopic analysis of photoreceptor degeneration in a congenitally blind strain of chickens is presented. The mutation was named rd, meaning 'retinal degeneration'. Although the chicks were behaviorally and electrophysiologically blind at the time of hatching, their retinas appeared morphologically comparable to normal chicks at this stage. Both groups had well-developed photoreceptor cells, although outer segments were typically disoriented or misaligned. In the normal, and to some degree in the rd, retina, outer segments became organized within the first week posthatching. In the rd retina at that time, however, more outer segments were disorganized and disoriented. Disc-like membranes were also seen in some inner segments. Many photoreceptors had distended inner segment tips containing a granular cytoplasm. Membraneous debris was present in the subretinal space. Over the next 2-3 weeks there was a reduction in number of inner segments, outer segments and photoreceptor nuclei of both rods and cones. Photoreceptor cell bodies in the outer nuclear layer were replaced by Mueller cell processes. By the end of the second month, a larger cone:rod ratio was apparent, and a large proportion of the remaining cones were double cones. Intact outer segments were rarely seen at that time. Few and sporadic cone cells, identified by a pale-staining oil droplet, were the predominant surviving photoreceptors by 6 months of age. At the later stages examined, the pigment epithelium (PE) appeared to be undergoing degenerative changes. A general thinning of cells and hypopigmentation of PE cells was apparent, although hyperpigmented, hypertrophied PE cells were also present which bulged into the subretinal space. Pigmented cells of unknown origin were also noted in the subretinal space at the later time points.

Neurotransmitter-specific identification and characterization of neurons in the all-cone retina of Anolis carolinensis. II: Glutamate and aspartate.

Immunocytochemical and autoradiographic methods were used to identify neurons in the pure cone retina of the lizard (Anolis carolinensis) that are likely to employ glutamate (GLU) or aspartate (ASP) as a neurotransmitter. GLU immunocytochemistry demonstrated high levels of endogenous GLU in all cone types and numerous bipolar cells. Moderate GLU levels were found in horizontal and ganglion cells. Müller cells and most amacrine cells had very low GLU levels. GLU immunoreactivity (GLU-IR) in the cones was present from the inner segment to the synaptic pedicle. A large spherical cell type with moderate GLU-IR was identified in the proximal inner plexiform layer (IPL). These cells also contain ASP and have been tentatively identified as amacrine cells. Uptake of [3H]-L-GLU labeled all retinal layers. All cone types and Müller cells sequestered [3H]-D-ASP, a substrate specific for the GLU transporter. Anti-ASP labeling was observed in cones, horizontal cells, amacrine cells, and cells in the ganglion cell layer. ASP immunoreactivity (ASP-IR) in the cones was confined to the inner segment. One ASP-containing pyriform amacrine cell subtype ramifying in IPL sublamina b was identified. Analysis of GLU-IR, ASP-IR, and GABA-IR on serial sections indicated that there were two distinct populations of horizontal cells in the Anolis retina: one containing GABA-IR, GLU-IR, and ASP-IR; and another type containing only GLU-IR and ASP-IR. Light GLU-IR was frequently found in GABA-containing amacrine cells but ASP-IR was not. The distinct distributions of GLU and ASP may indicate distinctly different roles for these amino acids. GLU, not ASP, is probably the major neurotransmitter in the cone-bipolar-ganglion cell pathway of the Anolis retina. Both GLU and ASP are present in horizontal cells and specific subpopulations of amacrine cells, but it is unclear if GLU or ASP have a neurotransmitter role in these cells.

[Alterations in concanavalin A binding during retinal development in Xenopus laevis]. / Modifications de la fixation de la concanavaline A au cours du développement de la rétine chez Xenopus laevis.

Changes in concanavalin A binding were observed in the retina of Xenopus laevis throughout development. Prior to stage 37, the optic cup and nervous sysetm displayed a light, diffuse staining. Abruptly at stage 37, however, intense staining reaction occurred in the ganglionic fibers, both plexiform layers and photoreceptor inner segments, remaining thus throughout larval and adult life. Our results suggest that important structural modifications occur in retinal cells at the time of establishment of connections with the tectum, preceedings, and possibility related to, electrical functioning of the visual system.