These unique characteristics allow the RPE to provide functional support to the neural retina and act to maintain metabolic homeostasis via:Īlthough the term "CHRPE" exclusively suggests hypertrophic cellular changes, histological analysis shows various morphologic cellular changes of CHRPE and its variants. Another notable feature of RPE cells is their high concentration of intracellular melanosomes, a cellular organelle that produces pigment granules known as melanin. These molecules act to absorb stray light and neutralize free radical oxygen species. Outer to the neural retina is the retinal pigmented epithelium (RPE), a single (simple) layer of cuboidal epithelial cells joined together by zonula occludens junctions. These tight junctions allow RPE cells to act as a gate, containing bidirectional pumps that regulate the transport of molecules to and from the choroid and neural retina. The neural retina comprises seven layers of various photosensitive neurons that synapse on one another along a cascade that ultimately terminates in the visual cortex of the occipital lobe for interpretation. The photoreceptor layer houses the cell bodies of rod and cone photoreceptors these cells contain visual pigments responsible for absorbing light and triggering the conversion of light photons into neurochemical signals, a process known as phototransduction. Disruption of the homeostatic balance between the RPE and neural retina is the basis for many of the most common retinal diseases. The underlying choroid and its blood supply also play a crucial role in this process these three structures must work together to maintain homeostatic balance and function properly. Truly, it comprises two distinct entities that work in concert with each other: the neural retina and the retinal pigmented epithelium. The retina is an ocular structure responsible for gathering gross visual stimuli that enter the eye and transforming them into neuronal signals transported to the brain for interpretation.
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