Song Weilin, Zhu Ruilin, Gao Wenna, Xing Chen, Yang Liu
Department of Ophthalmology, Peking University First Hospital, Beijing, China.
Front Med (Lausanne). 2022 Apr 26;9:831463. doi: 10.3389/fmed.2022.831463. eCollection 2022.
Damage to and death of the retinal pigment epithelium (RPE) are closely related to retinal degeneration. Blue light is a high-energy light that causes RPE damage and triggers inflammatory responses. This study investigates whether blue light induces RPE necroptosis, explores pharmacologic therapy and specific mechanisms, and provides hints for research on retinal degeneration.
The human RPE cell line ARPE-19 was cultured and subjected to blue light insult . Annexin V/PI was used to evaluate RPE survival. Minocycline was applied to inhibit the death of RPE. Proteomic measurement was used to analyze protein expression. Inhibitors of necroptosis and apoptosis were applied to assess the death mode. Immunofluorescence of protein markers was detected to analyze the mechanism of cell death. Subcellular structural changes were detected by transmission electron microscopy. Reactive oxygen species (ROS) was tested by DCFH-DA. Mitochondrial membrane potential (Δψ) was detected by JC-1. BALB/c mice received bule light exposure, and RPE flatmounts were stained for verification .
Blue light illumination induced RPE death, and minocycline significantly diminished RPE death. Proteomic measurement showed that minocycline effectively mitigated protein hydrolysis and protein synthesis disorders. Necroptosis inhibitors (Nec-1s, GSK-872) increased the survival of RPE cells, but apoptosis inhibitors (Z-VAD-FMK) did not. After blue light illumination, high-mobility group box-1 (HMGB1) was released from the nucleus, receptor-interacting protein kinase 3 (RIPK3) aggregated, and mixed-lineage kinase domain-like protein (MLKL) increased in the RPE. The application of minocycline alleviated the above phenomena. After blue light illumination, RPE cells exhibited necrotic characteristics accompanied by destruction of cell membranes and vacuole formation, but nuclear membranes remained intact. Minocycline improved the morphology of RPE. Blue light increased ROS and decreased Δψ of RPE, minocycline did not reduce ROS but kept Δψ stable. , HMGB1 release and RIPK3 aggregation appeared in the RPE of BALB/c mice after blue light illumination, and minocycline alleviated this effect.
Blue light exposure causes RPE necroptosis. Minocycline reduces the death of RPE by keeping Δψ stable, inhibiting necroptosis, and preventing HMGB1 release. These results provide new ideas for the pathogenesis and treatment of retinal degeneration.
视网膜色素上皮(RPE)的损伤和死亡与视网膜变性密切相关。蓝光是一种高能光,可导致RPE损伤并引发炎症反应。本研究调查蓝光是否诱导RPE坏死性凋亡,探索药物治疗及具体机制,并为视网膜变性的研究提供线索。
培养人RPE细胞系ARPE-19并进行蓝光损伤。采用膜联蛋白V/碘化丙啶评估RPE存活情况。应用米诺环素抑制RPE死亡。采用蛋白质组学检测分析蛋白质表达。应用坏死性凋亡和凋亡抑制剂评估死亡模式。检测蛋白质标志物的免疫荧光以分析细胞死亡机制。通过透射电子显微镜检测亚细胞结构变化。用二氯荧光素二乙酸酯检测活性氧(ROS)。用JC-1检测线粒体膜电位(Δψ)。对BALB/c小鼠进行蓝光照射,并对RPE平铺片进行染色验证。
蓝光照射诱导RPE死亡,米诺环素显著减少RPE死亡。蛋白质组学检测表明,米诺环素有效减轻蛋白质水解和蛋白质合成紊乱。坏死性凋亡抑制剂(Nec-1s、GSK-872)提高RPE细胞存活率,但凋亡抑制剂(Z-VAD-FMK)无效。蓝光照射后,高迁移率族蛋白B1(HMGB1)从细胞核释放,受体相互作用蛋白激酶3(RIPK3)聚集,RPE中混合谱系激酶结构域样蛋白(MLKL)增加。米诺环素的应用减轻了上述现象。蓝光照射后,RPE细胞呈现坏死特征,伴有细胞膜破坏和空泡形成,但核膜保持完整。米诺环素改善了RPE的形态。蓝光增加RPE的ROS并降低其Δψ,米诺环素不降低ROS但保持Δψ稳定。蓝光照射后,BALB/c小鼠的RPE中出现HMGB1释放和RIPK3聚集,米诺环素减轻了这种效应。
蓝光照射导致RPE坏死性凋亡。米诺环素通过保持Δψ稳定、抑制坏死性凋亡和防止HMGB1释放来减少RPE死亡。这些结果为视网膜变性的发病机制和治疗提供了新思路。