用眼部输送色素上皮生成因子 (PEDF) 作为治疗地理萎缩的神经保护剂。

IF 7 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Emily F Warner, Laura Vaux, Kara Boyd, Peter S Widdowson, Katie M Binley, Andrew Osborne
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引用次数: 0

摘要

地理萎缩(GA)是老年性黄斑变性(AMD)的一种晚期形式,开始时是视网膜外层的萎缩性病变,然后扩大到覆盖黄斑和眼窝,随着时间的推移会导致严重的视力丧失。色素上皮细胞衍生因子(PEDF)具有多种特性,包括促进细胞存活、减轻炎症反应、抑制血管生成、对抗氧化应激、调节自噬和刺激抗凋亡通路等,因此是治疗老年性黄斑变性的理想候选药物。然而,由于 PEDF 蛋白的半衰期相对较短,需要频繁注射,因此不具备临床治疗 GA 的潜力。因此,我们介绍了 PEDF 基因的给药方法,比较和对比了病毒载体和非病毒载体的给药途径,并探讨了 PEDF 作为 GA 神经保护剂所面临的关键挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ocular delivery of Pigment Epithelium-Derived Factor (PEDF) as a neuroprotectant for Geographic Atrophy.

Geographic atrophy (GA) is an advanced form of age-related macular degeneration (AMD), that starts with atrophic lesions in the outer retina that expand to cover the macula and fovea, leading to severe vision loss over time. Pigment Epithelium-Derived Factor (PEDF) has a diverse-range of properties, including its ability to promote cell survival, reduce inflammation, inhibit angiogenesis, combat oxidative stress, regulate autophagy, and stimulate anti-apoptotic pathways, making it a promising therapeutic candidate for GA. However, the relatively short half-life of PEDF protein has precluded its potential as a clinical therapy for GA since it would require frequent injections. Therefore, we describe administration of a PEDF gene, comparing and contrasting delivery routes, viral and non-viral vectors, and consider the critical challenges for PEDF as a neuroprotectant for GA.

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来源期刊
Aging and Disease
Aging and Disease GERIATRICS & GERONTOLOGY-
CiteScore
14.60
自引率
2.70%
发文量
138
审稿时长
10 weeks
期刊介绍: Aging & Disease (A&D) is an open-access online journal dedicated to publishing groundbreaking research on the biology of aging, the pathophysiology of age-related diseases, and innovative therapies for conditions affecting the elderly. The scope encompasses various diseases such as Stroke, Alzheimer's disease, Parkinson’s disease, Epilepsy, Dementia, Depression, Cardiovascular Disease, Cancer, Arthritis, Cataract, Osteoporosis, Diabetes, and Hypertension. The journal welcomes studies involving animal models as well as human tissues or cells.
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