RETINAL-PIGMENT EPITHELIAL TRANSPORT MECHANISMS AND THEIR CONTRIBUTIONS TO THE ELECTRORETINOGRAM

Citation
Rp. Gallemore et al., RETINAL-PIGMENT EPITHELIAL TRANSPORT MECHANISMS AND THEIR CONTRIBUTIONS TO THE ELECTRORETINOGRAM, Progress in retinal and eye research, 16(4), 1997, pp. 509-566
Citations number
310
Categorie Soggetti
Ophthalmology
ISSN journal
13509462
Volume
16
Issue
4
Year of publication
1997
Pages
509 - 566
Database
ISI
SICI code
1350-9462(1997)16:4<509:RETMAT>2.0.ZU;2-N
Abstract
The translocation of ions, fluid and macromolecules across epithelia i s made possible by the asymmetric distribution of transport proteins, enzymes and receptors in two physically distinct plasma membrane domai ns that form the apical and basolateral sides of the cell. Each side f aces a different extracellular environment. In the back of the vertebr ate eye, the retinal pigment epithelium (RPE) apical membrane receives a continuous stream of paracrine signals that are generated by a vari ety of retinal neurons in the light and dark. These signals help regul ate RPE function, and conversely, alterations in RPE function can modi fy the activity of retinal neurons. At the basolateral surface, there is a continual exchange of nutrients and waste products, along with a flow of hormonal signals from the choroidal blood supply, all of which serve to maintain the health and integrity of the distal retina and i n particular. the photoreceptors. This review provides an integrated s ummary of the apical and basolateral membrane and intracellular signal ing mechanisms that mediate the vectorial traffic of ions and fluid ac ross the RPE. These same mechanisms help regulate the chemical milieu within the cell and in the extracellular spaces that surround the cell . They also generate specific components of the electrical (EGG). The last part of this review is focused on the light-induced photoreceptor -dependent decrease in subretinal potassium concentration ([K](o)) tha t occurs in the intact eye and serves as a paracrine signal for the RP E. This signal plays a central role in regulating RPE physiology and i n mediating retina/RPE interactions, following transitions between lig ht and dark; it is mimicked in vitro by a small (3 mM) change in [K](o ) on the apical side of the epithelium. The clinical implications are discussed in terms of the transport mechanisms that regulate hydration of the subretinal space and that potentially mediate fluid absorption out of the retina. (C) 1997 Elsevier Science Ltd.