Journal Article

Ferrostatin-1, a ferroptosis inhibitor, mitigates all-trans-retinal-induced retinal pigment epithelium degeneration in mice

Chen, Yuling, Shen, Xiaoqing, Wu, Yalin, He, Beiting, Xi, Ruitong, Chen, Jingmeng

2025

Overview

Background Disruption of the retinoid (visual) cycle causes all- trans -retinal (atRAL) to accumulate in photoreceptors and retinal pigment epithelium (RPE), contributing to Stargardt disease type 1 (STGD1) and dry age-related macular degeneration (dAMD). Yet, the mechanisms underlying atRAL-induced RPE degeneration are not well understood. Here, we explored whether ferroptosis, a form of regulated cell death marked by iron-dependent lipid peroxidation, mediated RPE damage by atRAL. Methods Cell and animal models of STGD1 and dAMD were established using ARPE-19 cells loaded with atRAL and Abca4 −/− Rdh8 −/− mice subjected to light exposure. Cell viability and morphology, mitochondrial morphology, ferrous iron (Fe 2+ ) levels, reactive oxygen species (ROS) production, lipid peroxidation, and ferroptosis-related gene and protein expression were assessed using MTS assay, inverted and confocal microscopy, fluorescence staining, quantitative real-time polymerase chain reaction (qRT-PCR), and Western blotting, respectively. The conditions of mouse retina were evaluated by electroretinography (ERG), optical coherence tomography (OCT), fundus imaging, and immunofluorescence labeling. Results atRAL triggered ferroptosis of ARPE-19 cells through Fe 2+ accumulation, ROS generation, lipid peroxidation, mitochondrial damage, and abnormal expression of typical ferroptosis-related genes and proteins. These effects were capable of being alleviated by treatment with ferrostatin-1 (Fer-1), a potent ferroptosis inhibitor. Moreover, ferroptosis was clearly observed in the RPE of light-exposed Abca4 −/− Rdh8 −/− mice that showed rapid and excessive accumulation of atRAL in the retina. Notably, intraperitoneal administration of Fer-1 effectively mitigated the degeneration of the RPE and photoreceptors and significantly ameliorated retinal function in Abca4 −/− Rdh8 −/− mice following light exposure. Conclusions Ferroptosis plays a critical role in RPE damage by atRAL. Inhibition of ferroptosis by Fer-1 may enhance RPE cell survival and prevent subsequent photoreceptor degeneration in STGD1 and dAMD.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Age / Age-related macular degeneration / Animal models / Animals / Apoptosis / ATP-Binding Cassette Transporters / Biomedical and Life Sciences / Biomedicine / Biomolecules / Cell culture / Cell death / Cell Line / Cell survival / Cell Survival - drug effects / Cell viability / Cells / Confocal microscopy / Cyclohexylamines - pharmacology / Cyclohexylamines - therapeutic use / Cytotoxicity / Development and progression / Disease Models, Animal / DNA damage / Electroretinograms / Epithelium / Ferroptosis / Ferroptosis - drug effects / Flow cytometry / Health aspects / Humans / Immunofluorescence / Iron / Iron - metabolism / Iron in the body / Kinases / Laboratory animals / Light emitting diodes / Lipid peroxidation / Lipid Peroxidation - drug effects / Lipids / Macular degeneration / Macular Degeneration - pathology / Medicine/Public Health / Mice / Mitochondria - drug effects / Mitochondria - metabolism / Morphology / Phenylenediamines - pharmacology / Phenylenediamines - therapeutic use / Photoreceptors / Polymerase chain reaction / Reactive oxygen species / Reactive Oxygen Species - metabolism / Retina / Retinal degeneration / Retinal Degeneration - chemically induced / Retinal Degeneration - drug therapy / Retinal Degeneration - pathology / Retinal pigment epithelium / Retinal Pigment Epithelium - drug effects / Retinal Pigment Epithelium - pathology / Retinaldehyde / Software / Stargardt disease / Translational Ophthalmology / Variance analysis / Western blotting