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一种源自色素上皮衍生因子(PEDF)的短肽通过激活视网膜色素上皮(RPE)细胞中的SLC7A11/谷胱甘肽(GSH)/谷胱甘肽过氧化物酶4(GPX4)途径来预防大鼠中碘酸钠诱导的视网膜变性。

A PEDF-Derived Short Peptide Prevents Sodium Iodate-Induced Retinal Degeneration in Rats by Activating the SLC7A11/GSH/GPX4 Pathway in the RPE Cells.

作者信息

Ho Tsung-Chuan, Tsai Shawn-H, Yeh Shu-I, Sun Ming-Hui, Tsao Yeou-Ping

机构信息

Department of Medical Research, Mackay Memorial Hospital, New Taipei City, Taiwan.

Department of Ophthalmology, Mackay Memorial Hospital, Taipei, Taiwan.

出版信息

J Cell Mol Med. 2025 Jul;29(14):e70693. doi: 10.1111/jcmm.70693.

Abstract

Retinal pigment epithelial (RPE) cell damage caused by oxidative stress is a key factor in the pathogenesis of dry age-related macular degeneration (AMD). 6dS peptide is derived from the neuroprotective motif of pigment epithelium-derived factor (PEDF) and has antioxidant effects. This study used the sodium iodate (SI, a chemical oxidant)-induced animal dry AMD model to investigate the 6dS-mediated antioxidant mechanism. 6dS reduced SI-induced cytotoxicity, including ferrous iron accumulation, lipid peroxidation, glutathione (GSH) depletion, and ferroptosis in ARPE-19 cells. SI injection in rats induced cell death and lipid peroxidation in the RPE layer, along with retinal atrophy and electrophysiological dysfunction, recapitulating features of dry AMD that were counteracted by 6dS eye drop treatment. Mechanistically, 6dS induced the expression of SLC7A11 (solute carrier family seven member 11) and glutathione peroxidase 4 (GPX4) to alleviate SI-induced GSH depletion and lipid peroxidation. Inhibitors targeting the PEDF receptor, SLC7A11, and GPX4 abolished the 6dS effect. Our study proposes an antioxidant mechanism through which PEDF receptor signalling links to the SLC7A11/GSH/GPX4 axis to alleviate intracellular redox imbalance. These findings suggest that 6dS eye drops may be a promising treatment for dry AMD.

摘要

氧化应激引起的视网膜色素上皮(RPE)细胞损伤是干性年龄相关性黄斑变性(AMD)发病机制中的关键因素。6dS肽源自色素上皮衍生因子(PEDF)的神经保护基序,具有抗氧化作用。本研究使用碘酸钠(SI,一种化学氧化剂)诱导的动物干性AMD模型来研究6dS介导的抗氧化机制。6dS降低了SI诱导的细胞毒性,包括亚铁离子积累、脂质过氧化、谷胱甘肽(GSH)耗竭以及ARPE-19细胞中的铁死亡。给大鼠注射SI会诱导RPE层细胞死亡和脂质过氧化,同时伴有视网膜萎缩和电生理功能障碍,模拟了干性AMD的特征,而6dS滴眼液治疗可抵消这些特征。从机制上讲,6dS诱导溶质载体家族7成员11(SLC7A11)和谷胱甘肽过氧化物酶4(GPX4)的表达,以减轻SI诱导的GSH耗竭和脂质过氧化。靶向PEDF受体、SLC7A11和GPX4的抑制剂消除了6dS的作用。我们的研究提出了一种抗氧化机制,通过该机制PEDF受体信号传导与SLC7A11/GSH/GPX4轴相连,以减轻细胞内氧化还原失衡。这些发现表明,6dS滴眼液可能是治疗干性AMD的一种有前景的方法。

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