An understanding of the histology of the retina is essential to consider for complete insight into diseases involving a vital sensory component in the eye. The complexity of the retina, from its precise multi-layered structure to its various cell types and function, will be discussed briefly in this overview. Also, understanding features involving both structure and function will help appreciate the pathophysiology of disorders affecting the retina. Acknowledging the elements in this article may help guide future investigations towards specific therapeutic targets to help prevent, preserve, and treat irreversible vision loss.
Six major cell types form the various layers within the human retina :
The retina transmits light signals into chemical signals that are sent to the brain. This process requires the ability to sense the stimulus of light and transmit that signal from cell to cell.
Photoreceptors (rods and cones): The detection of light begins at the deepest cell layer in the retina, the photoreceptors, located in the outer nuclear layer. Rods are very light sensitive and are responsible for dim-light vision. Cones, on the other hand, are not very light sensitive but are specific for a particular wavelength of light. Thus, cones are responsible for high acuity color vision.
Bipolar cells: Photoreceptors use the neurotransmitter, glutamate, to communicate at the synapse with bipolar cells within the outer plexiform layer. Bipolar cell bodies are just shallow to this layer at the inner nuclear layer. At the inner plexiform layer, bipolar cells are responsible for transmitting an impulse to retinal ganglion cells.
Retinal ganglion cells: These are the final receivers and transmitters of the initial stimulus. They send the information they receive down their axons, which eventually form the optic nerve and project to higher brain centers.
Amacrine cells: Amacrine cells modulate the excitation of the retinal ganglion cells through contact with ganglion cell dendrites or bipolar cell axon terminal bulbs, using the neurotransmitters GABA and glycine.
Horizontal cells: These cells function to modulate the communication between photoreceptors and bipolar cells. Bipolar cells contact ganglion and amacrine cells at the inner plexiform layer.
Müller cells: These are cells are of glial origin and are essential for proper retinal function. They contact almost every cell type in the retina, spanning the entire width from the photoreceptors to the inner retina. They serve to recycle neurotransmitters, prevent glutamate toxicity, and regulate nutrient homeostasis in the retina.
Retinal tissue can be utilized from post-mortem, enucleated eyes. Following dissection, the retina can undergo fixing via 4% paraformaldehyde (PFA) in 0.1 M phosphate buffer (PB), pH 7.4, for 10 or 30 minutes at room temperature (RT). They can then be stored in sucrose at −20°C for cryoprotection until use. Once vertically sliced, the retina is visualizable with the use of various lab microscopes.
Depending on the investigator's area of interest, various procedures can be used to visualize the retina.
Fluorescent-labeled immunochemistry has played a significant role in retina histology as well as other fields for its ability to target a certain cell population. The following are proteins isolated in certain retinal cells that can be targetted via antibodies :
Photoreceptors (rods and cones): Rods and cones contain both an outer and inner segment, and their structural distinction are visible via an electron microscope. The outer segments of rod include a set of membranous discs that resemble a stack of coins. On the other hand, the outer segments of cones contain infoldings of the surface membrane that taper slightly, giving the cones their name. The outer plexiform layer, the connection between the photoreceptors and the bipolar cells, can also be appreciated under electron microscopy.
Bipolar cells: Bipolar cells are unique in that they have both a dendritic process above and an axon terminal below.
Retinal ganglion cells: These cells present as having a large cell body with a dendritic tree.
Amacrine cells: The processes of these cells have characteristics of both axons and dendrites, allowing for pre- and postsynaptic transmission.
Muller cells: These are unique looking cells as they can be characterized by their length, extending from the outer nuclear layer to the most inner retina.
Diseases of the retina divide into two categories, those involving the death of photoreceptors (rods and cones) at the outer nuclear layer and those involving cells in the inner retina such as the bipolar and ganglion cells.
Diseases of the photoreceptors (rods and cones) are characterizable by their pattern of cellular and visual loss.
Diseases of the inner retina:
When viewed using histological methods, retinal pathology can appear structurally disorganized. For example, rosette-like structures can present in diseases of the retina, including retinitis pigmentosa, diabetic retinopathy, and retinoblastoma.
When posterior uveitis secondary to infection or malignancy of unknown origin is suspected, chorioretinal biopsy and subsequent histopathological analysis along with appropriate history and physical exams and additional ancillary testing including B-scan ultrasonography, optical coherence tomography (OCT), and fluorescein angiography, can help aid coming to an appropriate diagnosis.
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