학술논문

A novel AhR ligand, 2AI, protects the retina from environmental stress.
Document Type
article
Source
Scientific reports. 6(1)
Subject
Retina
Cell Line
Animals
Mice
Inbred BALB C
Mice
Inbred C57BL
Humans
Mice
Reactive Oxygen Species
Aldehydes
Indoles
Fatty Acids
Unsaturated
Receptors
Aryl Hydrocarbon
RNA
Small Interfering
Protective Agents
Ligands
Signal Transduction
Apoptosis
RNA Interference
Lipid Peroxidation
Light
Retinal Pigment Epithelium
Polychlorinated Dibenzodioxins
Fatty Acids
Unsaturated
Inbred BALB C
Inbred C57BL
RNA
Small Interfering
Receptors
Aryl Hydrocarbon
Language
Abstract
Various retinal degenerative diseases including dry and neovascular age-related macular degeneration (AMD), retinitis pigmentosa, and diabetic retinopathy are associated with the degeneration of the retinal pigmented epithelial (RPE) layer of the retina. This consequently results in the death of rod and cone photoreceptors that they support, structurally and functionally leading to legal or complete blindness. Therefore, developing therapeutic strategies to preserve cellular homeostasis in the RPE would be a favorable asset in the clinic. The aryl hydrocarbon receptor (AhR) is a conserved, environmental ligand-dependent, per ARNT-sim (PAS) domain containing bHLH transcription factor that mediates adaptive response to stress via its downstream transcriptional targets. Using in silico, in vitro and in vivo assays, we identified 2,2'-aminophenyl indole (2AI) as a potent synthetic ligand of AhR that protects RPE cells in vitro from lipid peroxidation cytotoxicity mediated by 4-hydroxynonenal (4HNE) as well as the retina in vivo from light-damage. Additionally, metabolic characterization of this molecule by LC-MS suggests that 2AI alters the lipid metabolism of RPE cells, enhancing the intracellular levels of palmitoleic acid. Finally, we show that, as a downstream effector of 2AI-mediated AhR activation, palmitoleic acid protects RPE cells from 4HNE-mediated stress, and light mediated retinal degeneration in mice.