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A Novel HDL-Mimetic Peptide HM-10/10 Protects RPE and Photoreceptors in Murine Models of Retinal Degeneration

机译:一种新型的HDL模拟肽HM-10 / 10在视网膜变性的鼠模型中保护RPE和感光器。

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摘要

Age-related macular degeneration (AMD) is a leading cause of blindness in the developed world. The retinal pigment epithelium (RPE) is a critical site of pathology in AMD. Oxidative stress plays a key role in the development of AMD. We generated a chimeric high-density lipoprotein (HDL), mimetic peptide named HM-10/10, with anti-oxidant properties and investigated its potential for the treatment of retinal disease using cell culture and animal models of RPE and photoreceptor (PR) degeneration. Treatment with HM-10/10 peptide prevented human fetal RPE cell death caused by tert-Butyl hydroperoxide (tBH)-induced oxidative stress and sodium iodate (NaIO3), which causes RPE atrophy and is a model of geographic atrophy in mice. We also show that HM-10/10 peptide ameliorated photoreceptor cell death and significantly improved retinal function in a mouse model of N-methyl-N-nitrosourea (MNU)-induced PR degeneration. Our results demonstrate that HM-10/10 protects RPE and retina from oxidant injury and can serve as a potential therapeutic agent for the treatment of retinal degeneration.
机译:与年龄有关的黄斑变性(AMD)是发达国家失明的主要原因。视网膜色素上皮(RPE)是AMD病理的关键部位。氧化应激在AMD的发展中起着关键作用。我们生成了具有抗氧化特性的嵌合高密度脂蛋白(HDL)模拟肽HM-10 / 10,并使用RPE和光感受器(PR)的细胞培养和动物模型研究了其治疗视网膜疾病的潜力。用HM-10 / 10肽治疗可预防由氢过氧化叔丁基(tBH)诱导的氧化应激和碘酸钠(NaIO3)引起的人胎RPE细胞死亡,后者可引起RPE萎缩,是小鼠地理萎缩的模型。我们还显示,在N-甲基-N-亚硝基脲(MNU)诱导的PR变性的小鼠模型中,HM-10 / 10肽改善了感光细胞的死亡并显着改善了视网膜功能。我们的结果表明,HM-10 / 10保护RPE和视网膜免受氧化损伤,并可以作为治疗视网膜变性的潜在治疗剂。

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