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In Vitro Gene Delivery in Retinal Pigment Epithelium Cells by Plasmid DNA-Wrapped Gold Nanoparticles

机译:质粒DNA包裹的金纳米粒子在视网膜色素上皮细胞中的体外基因传递。

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摘要

Many rare diseases course with affectation of neurosensory organs. Among them, the neuroepithelial retina is very vulnerable due to constant light/oxidative stress, but it is also the most accessible and amenable to gene manipulation. Currently, gene addition therapies targeting retinal tissue (either photoreceptors or the retinal pigment epithelium), as a therapy for inherited retinal dystrophies, use adeno-associated virus (AAV)-based approaches. However, efficiency and safety of therapeutic strategies are relevant issues that are not always resolved in virus-based gene delivery and alternative methodologies should be explored. Based on our experience, we are currently assessing the novel physical properties at the nanoscale of inorganic gold nanoparticles for delivering genes to the retinal pigment epithelium (RPE) as a safe and efficient alternative approach. In this work, we present our preliminary results using DNA-wrapped gold nanoparticles (DNA-gold NPs) for successful in vitro gene delivery on human retinal pigment epithelium cell cultures, as a proof-of-principle to assess its feasibility for retina in vivo gene delivery. Our results show faster expression of a reporter gene in cells transfected with DNA-gold NPs compared to DNA-liposome complexes. Furthermore, we show that the DNA-gold NPs follow different uptake, internalization and intracellular vesicle trafficking routes compared to pristine NPs.
机译:许多罕见疾病会随着神经感觉器官的影响而发展。其中,由于持续的光/氧化应激,神经上皮视网膜非常脆弱,但它也是最容易获得和接受基因操作的地方。目前,针对视网膜组织(光感受器或视网膜色素上皮)的基因添加疗法,作为遗传性视网膜营养不良的疗法,使用了基于腺相关病毒(AAV)的方法。但是,治疗策略的效率和安全性是相关问题,在基于病毒的基因传递中并不总是能够解决的,应探索替代方法。基于我们的经验,我们目前正在评估无机金纳米颗粒在纳米尺度上用于将基因传递到视网膜色素上皮(RPE)的新颖物理特性,以此作为一种安全有效的替代方法。在这项工作中,我们介绍了使用DNA包裹的金纳米颗粒(DNA-金NP)在人类视网膜色素上皮细胞培养物中成功进行体外基因递送的初步结果,作为评估其在体内视网膜可行性的原理证明基因传递。我们的结果表明,与DNA-脂质体复合物相比,报道基因在用DNA-金纳米颗粒转染的细胞中表达更快。此外,我们显示,与原始NP相比,DNA-金NP遵循不同的摄取,内化和细胞内囊泡运输途径。

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