학술논문

Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia.
Document Type
article
Source
Cell Reports. 42(8)
Subject
11-cis-retinal
CP: Cell biology
CP: Neuroscience
Müller cells
chromophore
cone opsin
photic visual cycle
photoisomerization
retina
retinal pigmented epithelium
vision
visual cycle
Animals
Mice
Retinal Pigment Epithelium
Retinaldehyde
Retinal Pigments
Receptors
G-Protein-Coupled
Neuroglia
Retinal Cone Photoreceptor Cells
Language
Abstract
In daylight, demand for visual chromophore (11-cis-retinal) exceeds supply by the classical visual cycle. This shortfall is compensated, in part, by the retinal G-protein-coupled receptor (RGR) photoisomerase, which is expressed in both the retinal pigment epithelium (RPE) and in Müller cells. The relative contributions of these two cellular pools of RGR to the maintenance of photoreceptor light responses are not known. Here, we use a cell-specific gene reactivation approach to elucidate the kinetics of RGR-mediated recovery of photoreceptor responses following light exposure. Electroretinographic measurements in mice with RGR expression limited to either cell type reveal that the RPE and a specialized subset of Müller glia contribute both to scotopic and photopic function. We demonstrate that 11-cis-retinal formed through photoisomerization is rapidly hydrolyzed, consistent with its role in a rapid visual pigment regeneration process. Our study shows that RGR provides a pan-retinal sink for all-trans-retinal released under sustained light conditions and supports rapid chromophore regeneration through the photic visual cycle.