PubMed HealthSearch

SEARCH · PubMed Health

Results for “Retinal Cone Photoreceptor Cells”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 19 recordsLinked to original sources

Developmental analysis of the cone photoreceptor-less little skate retina reveals distinct Onecut1 isoforms.

The retinal development of elasmobranchs, the subclass comprising sharks, skates, and rays, remains poorly understood. This group is diverse in retinal phenotype, with many sharks and rays possessing rods together with one or more cone types. In contrast, the little skate (Leucoraja erinacea) has only a single rod photoreceptor type, which has been reported to exhibit some physiological and anatomical properties associated with cones. To investigate how this unusual photoreceptor system develops, we first identified an embryonic stage of early photoreceptor formation based on otx2 expression. We then developed a retinal electroporation approach to test whether a onecut1-dependent cone-associated reporter could be activated in the embryonic skate retina. Activation of this reporter was not detected, indicating that the corresponding enhancer is not robustly active under the conditions tested. To assess developmental changes in gene expression, we generated bulk RNA-seq datasets from embryonic, hatchling, and adult retinas. These analyses showed strong embryonic expression of onecut1, increasing expression of rod-associated genes through development, and pseudogenization or loss of multiple cone-enriched genes. We further identified a developmentally regulated onecut1 splice isoform containing an additional 48 amino acid sequence between the CUT and homeodomain DNA-binding domains. This spacer-containing isoform, termed LSOC1X2, was most abundant in the embryonic retina. To test whether LSOC1X2 retained regulatory activity, we assayed it in a mouse retinal reporter system. Both skate Onecut1 isoforms activated the ThrbCRM1 reporter in this heterologous context. Together, these findings identify a novel, developmentally regulated retinal onecut1 isoform in the little skate and establish it as a candidate regulator for future studies of photoreceptor development in this species and its elasmobranch relatives.

Animals

Cone inputs to ganglion cells in hereditary retinal degeneration.

The photoreceptor layer degenerated, but cone nuclei apparently devoid of outer segments were retained in retinas of aged rats of the Royal College of Surgeons strain from which optic tract activity was recorded. Measures of sensitivity showed these single axons of retinal ganglion cells to have photopic spectral responses. Cone remnants containing a cone pigment may be the photoreceptive elements in these retinas.

Action Potentials

Systematic discovery of retina-enriched Rik genes identifies 1190005I06Rik as a novel modulator of visual signalling.

BACKGROUND: High‑throughput transcriptome projects have revealed thousands of mammalian genes with little or no functional annotation. Among these are hundreds of loci assigned provisional “Rik” identifiers following discovery in the RIKEN cDNA annotation effort. Although often dismissed as genomic dark matter, such genes may encode tissue‑restricted proteins that modulate physiologic functions and influence disease. The retina is a highly specialised neural tissue and a common site of inherited disorders; understanding its molecular repertoire could illuminate novel therapeutic avenues. METHODS: We integrated bulk RNA‑seq from ten adult mouse tissues, evolutionary and domain analysis, single‑cell RNA‑seq, and CRISPR/Cas9 gene disruption to systematically catalogue protein‑coding Rik genes enriched in the retina and test the function of a representative gene. RESULTS: A rigorous differential expression analysis identified 44 Rik genes with robust retina‑specific expression compared with nine non‑retinal tissues. Many of these genes lack orthologues beyond rodents, while others show broad conservation, illustrating a continuum from lineage‑restricted to conserved retinopathy candidates. Single‑cell transcriptomics revealed that these genes are expressed across retinal cell types, with the highest aggregate expression in cone photoreceptors and inner interneurons. To evaluate physiological significance, we generated a 1190005I06Rik knockout mouse. Although retinal architecture appeared normal, loss of 1190005I06Rik enhanced electroretinogram b‑wave amplitudes and altered light‑avoidance behaviour, indicating that this previously uncharacterised gene acts as a negative modulator of visual signalling. CONCLUSIONS: We present a curated atlas of retina‑enriched Rik genes and demonstrate that 1190005I06RIK modulates retinal circuit function. This resource expands the molecular landscape of the retina and provides new candidates for the genetic basis of inherited retinal disease. Our findings underscore that unannotated genes may exert measurable effects on sensory processing and warrant systematic exploration in the context of human ocular disorders.

Animals

Long-term functional synaptic integration of genome-edited retinal organoids in a primate model of macular degeneration.

Retinal organoids represent a promising regenerative strategy for restoring vision in retinal degenerative diseases, but the capacity of host cone bipolar cells in the primate macula to rewire with transplanted photoreceptors has not been established. In this study, we transplanted genome-edited ISL1-/- human retinal organoids lacking ON-bipolar cells into an acute laser-induced macular photoreceptor ablation non-human primate model. Using immunohistochemistry, ultrastructural imaging, and focal macular electroretinography, we demonstrate that host rod and cone bipolar cells actively extend dendrites toward grafted photoreceptors and form synaptic contacts, with evidence of functional signal transmission in a subset of transplanted eyes. Longitudinal, per-eye analyses revealed that host ON-bipolar responses improved in two of four eyes with ISL1-/- graft by up to 21.6% and remained stable for up to 2 years post transplantation. Moreover, OFF-pathway connectivity showed potential progressive maturation, with delayed increase in d-wave after 13 months in one of those eyes. These findings provide the first demonstration of long-term anatomical host-graft synaptic integration in the primate macula, establishing that central cone bipolar circuits retain the capacity for durable rewiring with human stem-cell-derived grafts. Our results highlight ISL1-/- retinal organoids as a promising approach for central vision restoration in macular degeneration.

Animals

Immunocytochemical localization of opsin in outer segments and Golgi zones of frog photoreceptor cells. An electron microscope analysis of cross-linked albumin-embedded retinas.

Adult vertebrate retinal cells (rod and cones) continuously synthesize membrane proteins and transport them to the organelle specialized for photon capture, the outer segment. The cell structures involved in the synthesis of opsin have been identified by means of immunocytochemistry at the electron microscope level. Two indirect detection systems were used: (a) rabbit antibodies to frog opsin were localized with ferritin conjugated F(ab')2 of sheep antibodies to rabbit F(ab')2 and (b) sheep antibodies to cattle opsin were coupled to biotin and visualized by means of avidin-ferritin conjugates (AvF). The reagents were applied directly to the surface of thin sections of frog retinal tissues embedded in glutaraldehyde cross-linked bovine serum albumin (BSA). Specific binding of anti-opsin antibodies indicates that opsin is localized in the disks of rod outer segments (ROS), as expected, and in the Golgi zone of the rod cell inner segments. In addition, we observed quantitatively different labeling patterns of outer segments of rods and cones with each of the sera employed. These reactions may indicate immunological homology of rod and cone photopigments. Because these quantitiative variations of labeling density extend along the entire length of the outer segment, they also serve to identify the cell which has shed its disks into adjacent pigment ipithelial cell phagosomes.

Animals

[Recovery of rod and cone systems after retinal detachment surgery].

The paper reports on the threshold values for light perception of circumscript retinal areas for different adaptation levels in patients successfully operated for retinal detachment. The examinations were carried out by means of the Tübingen projection perimeter, using the method of static perimetry in a meridian containing an approximately equal area of healthy and of formerly detached retina. The main aim of this examination was to establish whether both retinal photoreceptor systems recover within the same time after the operation. There is various evidence that the restitutions of the rod and cone systems do not occur at the same time.

Humans

Vitamin E deficiency and the retina: photoreceptor and pigment epithelial changes.

To investigate the role of normal vitamin E levels and the interrelationships between vitamin E and A in maintaining the visual cells of the retina, weanling female Sprague-Dawley rats were fed vitamin E-free diets differing tenfold in their vitamin A content (0.8 and 8.0 mg of retinol per kilogram of diet). Rats on vitamin E-free diets with the higher vitamin A level exhibited marked disruption of photoreceptor outer segment membranes and a fivefold increase in the number of lipofuscin granules in the pigment epithelial cells which ingest these membranes. Rats on vitamin E-free diets with the lower vitamin A level showed the same retinal damages plus significant loss of photoreceptor cells compared to age-matched rats on control diets. Rods and cones were involved equally, and their pattern of loss was not like that found in vitamin A deficiency. Normal levels of vitamin E probably protect photoreceptor membranes from oxidative damage and retard the accumulation of their remnants and other products of lipid breakdown in the pigment epithelium. The vitamin A status of rats has a significant influence on the extent of damage induced by vitamin E deficiency.

Animals

[Cone dysfunction and cone dystrophy. A dynamic classification (author's transl)].

Since Goodman and coll. introduced the concept of cone dysfunction syndromes, many papers have been published. Some authors based their diagnosis on functional data while others referred to the classic denominations. As a consequence there is no uniformity with regard to terminology of the cone dystrophies. In an effort to avoir the introduction of new terms the author presents a classification of cone dysfunctions based on the results of electroretinography and color vision examination. This classification is dynamic since it allows the follow-up of a cone dystrophy into its late stages.

Color Perception

After-effects of small adapting fields.

1. Sensitivity to a small test probe in the centre of a small, steady background is less than when the background is large (sensitization). When an equiluminous steady annulus is added to the region surrounding a small background, rod threshold takes several minutes to stabilize at its new, lower level. The after-effects of the small background follow a time course characteristic of cortical adaptation. 2. The sensitivity loss and time course of recovery after intense bleaching lights in the cone system depend markedly on the size of the retinal region bleached, although no such effect is observed in the rod system. If a steady annular surround is added to the region surrounding the bleached patch, threshold falls rapidly to the value it would have after a large-area bleach of the same intensity. 3. The interaction between bleaches and steady surrounds suggests that bleaches produce long-lasting signals in the cone receptors. 4. The different temporal properties of sensitization on rod backgrounds and sensitization after cone bleaches suggest that different mechanisms underlie the two phenomena. 5. In cone vision, if light is added to the area surrounding a small, steady background, the subsequent readjustment takes minutes to complete, as it does in rod vision. But in addition, for cones, a large proportion of the sensitivity loss caused by the small background can be rapidly restored, as it is with cone bleaches. 6. The above results, together with the known absence of sensitization in rod dark adaptation, are consistent with the hypothesis that sensitization occurs at least partly at the retinal level in the cone system, but not (or only weakly) in the rod system, and that there is an additional, probably cortical elevation, common to rod and cone systems, for small backgrounds, but not for small, brief bleaches.

Adaptation, Ocular

The effects of hypophysectomy on the retinomotor responses of the killifish, Fundulus heteroclitus.

This paper presents the results of an investigation concerned with the effects of long-term hypophysectomy on the retinomotor responses of the euryhaline killifish, Fundulus heteroclitus: 1. The eye of hypophysectomised Fundulus heteroclitus responds to light and dark in the same manner as that of intact controls: the retina is not in a state of permanent light-adaptation as claimed by Vilter (1942) for the hypophysectomised eel. 2. There is no evidence of a persistent circadian rhythm during continous darkness. 3. Unilateral illumination of the eye of intact fish results in dispersion of retinal pigment in both illuminated and unilluminated eyes, as in the goldfish (Ali, 1964), but no such contralateral response was evident after hypophysectomy. The cones are unresponsive.

Adaptation, Physiological

The retinal pigment epithelium and photoreceptor cells. Light- and electron microscopic studies on monkey eyes.

In the perifoveal retina of the monkey, Cercopithecus aethiops, the melanin granules are accumulated in apical cytoplasmatic protrusions of the pigment epithelial cells, facing the end of the cones. The rods are inserted deeper into the pigment epithelium than the cones; they reach the bottom of the infoldings of the apical surface membrane of the pigment epithelial cells. No melanin granules or other inclusions are situated at the end of the rods. The outer extremity of the rods is considerably inclined and in sections often appears as groups of rod discs which are incompletely or completely separated from the main part of the outer segments. This separation is regarded as an artifact caused by the inclination of the rods, and it is therefore not considered to represent phagocytosis of the outer segments by the pigment epithelium. The inclusions of the pigment epithelial cells are classified in five categories which seem to be related to each other owing to their shared structural characteristics. It is suggested that melanin granules are produced, modified and destroyed by the pigment epithelial cells of the adult. Because of the relations between the photoreceptors and the melanin granules it is suggested that light scattered by the melanin granules may pass backwards through the outer segments of the cones, but not of the rods.

Animals

Chromatic patterns of cone photoreceptors. 1976 Glenn A. Fry Award Lecture.

The operations of vertebrate visual neurons must eventually be expressed in terms of the spectral classes and spatial distributions of photoreceptors that constitute inputs to those neurons. By using a cytochemical probe that permits visualization of the responses of cone photoreceptors to light stimulation, it has been possible to describe the spectral classes and spatial patterns of cones in a lower vertebrate, the goldfish, and in a primate, the baboon. This information is an important first step in analyzing the connections between cones and retinal neurons.

Animals

Transmission from photoreceptors to ganglion cells in turtle retina.

1. Synaptic transfer between photoreceptors and impulse-generating cells was studied in isolated eyecups from turtles. Single red-sensitive cones or rods were stimulated by current passed through an intracellular electrode, and impulses generated by the resulting synaptic action were recorded with an external micro-electrode. This technique permits study of retinal transmission without the operation of the visual transduction mechanism. Antidromic stimulation of the optic nerve indicated that most of the impulse-generating cells were ganglion cells.2. Individual ganglion cells responded transiently to changes in the membrane potential of a receptor and could be classified into three groups on the basis of the direction of the effective change in potential. Off centre ganglion cells responded selectively to depolarizations of a receptor, while on centre ganglion cells responded selectively to hyperpolarizations. On-off ganglion cells responded to both depolarizations and hyperpolarizations of a receptor.3. Ganglion cells gave the same pattern of response to electrical hyperpolarization of a receptor and to light in the centre of their receptive fields. Subthreshold depolarizing currents passed in a receptor antagonized the ganglion cell's response to light, and subthreshold hyperpolarizing currents reinforced the response. These observations are consistent with the view that the hyperpolarization generated by visual transduction is responsible for regulating the release of transmitter at the first retinal synapse.4. When a receptor was stimulated with weak current pulses of fixed intensity the number and latency of the ganglion cell impulses fluctuated randomly in successive trials. The relation between the fraction of trials yielding a response and the stimulus intensity was broad. These results indicate that the link between retinal input and output is noisy.5. In the most sensitive pairs of cells, a response of one or more impulses could be obtained in half the trials with a current of about 2 x 10(-11) A, which changed the potential of the receptor by 1-2 mV. A current of similar magnitude would be developed by about 130 photoisomerizations in a red-sensitive cone or 50 photoisomerizations in a rod.6. Dim background light producing a steady hyperpolarization of a few millivolts in the rods raised the threshold for electrically-evoked transmission from a rod to a ganglion cell. In experiments on red-sensitive cones, background light raised the threshold in the off pathway, in which depolarization was the effective stimulus, and lowered the threshold in the on pathway, in which hyperpolarization was the effective stimulus. These changes in sensitivity were not accompanied by obvious changes in the input resistance of the stimulated receptor. Regulation of retinal sensitivity in background light thus involves changes in synaptic transfer as well as changes in the sensitivity of the visual transduction mechanism.

Animals