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CD44 aptamer mediated cargo delivery to lysosomes of retinal pigment epithelial cells to prevent age-related macular degeneration

机译:CD44适体介导的货物运送到视网膜色素上皮细胞的溶酶体以防止与年龄有关的黄斑变性

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摘要

Age related macular degeneration (AMD) is a progressive, neurodegenerative disorder that leads to the severe loss of central vision in elderlies. The health of retinal pigment epithelial (RPE) cells is critical for the onset of AMD. Chronic oxidative stress along with loss of lysosomal activity is a major cause for RPE cell death during AMD. Hence, development of a molecule for targeted lysosomal delivery of therapeutic protein/drugs in RPE cells is important to prevent RPE cell death during AMD. Using human RPE cell line (ARPE-19 cells) as a study model, we confirmed that hydrogen peroxide (H2O2) induced oxidative stress results in CD44 cell surface receptor overexpression in RPE cells; hence, an important target for specific delivery to RPE cells during oxidative stress. We also demonstrate that the known nucleic acid CD44 aptamer - conjugated with a fluorescent probe (FITC) - is delivered into the lysosomes of CD44 expressing ARPE-19 cells. Hence, as a proof of concept, we demonstrate that CD44 aptamer may be used for lysosomal delivery of cargo to RPE cells under oxidative stress, similar to AMD condition. Since oxidative stress may induce wet and dry AMD, both, along with proliferative vitreoretinopathy, CD44 aptamer may be applicable as a carrier for targeted lysosomal delivery of therapeutic cargoes in ocular diseases showing oxidative stress in RPE cells.
机译:年龄相关性黄斑变性(AMD)是一种进行性神经退行性疾病,导致老年人严重丧失中央视力。视网膜色素上皮(RPE)细胞的健康对于AMD的发作至关重要。慢性氧化应激以及溶酶体活性的丧失是AMD期间RPE细胞死亡的主要原因。因此,开发用于在RPE细胞中靶向溶酶体递送治疗性蛋白质/药物的分子对于预防AMD期间RPE细胞死亡是重要的。以人类RPE细胞系(ARPE-19细胞)为研究模型,我们证实了过氧化氢(H2O2)诱导的氧化应激导致RPE细胞中CD44细胞表面受体的过度表达。因此,在氧化应激期间特异性递送至RPE细胞的重要靶标。我们还证明了与荧光探针(FITC)偶联的已知核酸CD44适体被传递到CD44表达ARPE-19细胞的溶酶体中。因此,作为概念的证明,我们证明了CD44适体可用于在氧化应激下,类似于AMD条件,将货物溶酶体递送至RPE细胞。由于氧化应激可诱导干性和湿性AMD,以及增殖性玻璃体视网膜病变,因此CD44适体可用作在RPE细胞中显示氧化应激的眼部疾病中靶向性溶酶体递送治疗性药物的载体。

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