Abstract

Age-related macular degeneration (AMD) is the progressive degeneration of the retinal pigment epithelium (RPE), retina, and choriocapillaris among elderly individuals and is the leading cause of blindness worldwide. Thus, a better understanding of the underlying mechanisms in retinal tissue activated by blue light exposure is important for developing novel treatment and intervention strategies. In this study, blue-light-emitting diodes with a wavelength of 440 nm were applied to RPE cells at a dose of 3.7 ± 0.75 mW/cm2 for 24 h. ARPE-19 cells were used to investigate the underlying mechanism induced by blue light exposure. A trypan blue exclusion assay was used for the cell viability determination. Flow cytometry was used for apoptosis rate detection and autophagy analysis. An immunofluorescence microscopy analysis was used to investigate cellular oxidative stress and DNA damage using DCFDA fluorescence staining and an anti-γH2AX antibody. Blue light exposure of zebrafish larvae was established to investigate the effect on retinal tissue development in vivo. To further demonstrate the comprehensive effect of blue light on ARPE-19 cells, next-generation sequencing (NGS) was performed for an ingenuity pathway analysis (IPA) to reveal additional related mechanisms. The results showed that blue light exposure caused a decrease in cell proliferation and an increase in apoptosis in ARPE-19 cells in a time-dependent manner. Oxidative stress increased during the early stage of 2 h of exposure and activated DNA damage in ARPE-19 cells after 8 h. Furthermore, autophagy was activated in response to blue light exposure at 24–48 h. The zebrafish larvae model showed the unfavorable effect of blue light in prohibiting retinal tissue development. The RNA-Seq results confirmed that blue light induced cell death and participated in tissue growth inhibition and maturation. The current study reveals the mechanisms by which blue light induces cell death in a time-dependent manner. Moreover, both the in vivo and NGS data uncovered blue light’s effect on retinal tissue development, suggesting that exposing children to blue light could be relatively dangerous. These results could benefit the development of preventive strategies utilizing herbal medicine-based treatments for eye diseases or degeneration in the future.

Highlights

  • Visual defects have a significant negative impact on the quality of life, and this causes an economic burden worldwide

  • Assay, the data showed that blue light induced significant cytotoxicity after 10 h of exposure, and the cell viability was less than 40% after 48 h of blue light exposure (Figure 1B)

  • The results suggest that blue light induced significant ARPE-19 cell death during long-term exposure, and apoptosis could be one of the causes of cell death; cell toxicity might be due to the activation of pro-apoptosis regulators and inhibition of cell cycle checkpoint gene expression

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Summary

Introduction

Visual defects have a significant negative impact on the quality of life, and this causes an economic burden worldwide. Age-related macular degeneration (AMD) is caused by severe loss of vision in the elderly. AMD is caused by the degeneration of retinal pigment epithelium (RPE) cells and cone photoreceptor cells responsible for light detection in the macula, the central part of the retina. AMD is the most common etiology for which patients attend low-vision clinics. Lipofuscin, an aggregation of oxidized proteins, was reported to induce apoptosis through proteasome inhibition and pro-apoptotic protein dysregulation [1]. The propensity for RPE cells to be damaged or destroyed by excessive exposure to visible light may be of significance to retinal disorders characterized by enhancing the accumulation of the autofluorescent pigments that constitute lipofuscin, aggregates of oxidized proteins that induce apoptosis through proteasome inhibition and dysregulation of proapoptotic proteins [1]. The overaccumulation of autofluorescent lipofuscin could indicate cell aging and increase AMD development risk [3]

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