Department of Engineering Physics , Polytechnique Montréal , Montreal , Quebec , Canada , H3C 3A7.
Nano Lett. 2018 Nov 14;18(11):6981-6988. doi: 10.1021/acs.nanolett.8b02896. Epub 2018 Oct 12.
Vision loss caused by retinal diseases affects hundreds of millions of individuals worldwide. The retina is a delicate central nervous system tissue stratified into layers of cells with distinct roles. Currently, there is a void in treatments that selectively target diseased retinal cells, and current therapeutic paradigms present complications associated with off-target effects. Herein, as a proof of concept, we introduce an in vivo method using a femtosecond laser to locally optoporate retinal ganglion cells (RGCs) targeted with functionalized gold nanoparticles (AuNPs). We provide evidence that AuNPs functionalized with an antibody toward the cell-surface voltage-gated K channel subunit K1.1 can selectively deliver fluorescently tagged siRNAs or fluorescein isothiocyanate-dextran dye into retinal cells when irradiated with an 800 nm 100 fs laser. Importantly, neither AuNP administration nor irradiation resulted in RGC death. This system provides a novel, non-viral-based approach that has the potential to selectively target retinal cells in diseased regions while sparing healthy areas and may be harnessed in future cell-specific therapies for retinal degenerative diseases.
视网膜疾病导致的视力丧失影响着全球数亿人。视网膜是一种精细的中枢神经系统组织,分层排列着具有不同功能的细胞层。目前,针对病变视网膜细胞的治疗方法存在空白,而现有的治疗模式存在与脱靶效应相关的并发症。在此,作为概念验证,我们引入了一种使用飞秒激光在体内局部光解靶向金纳米粒子(AuNPs)的视网膜神经节细胞(RGC)的方法。我们提供的证据表明,用针对细胞表面电压门控 K 通道亚基 K1.1 的抗体功能化的 AuNPs,当用 800nm 100fs 激光照射时,可以将荧光标记的 siRNA 或异硫氰酸荧光素标记的葡聚糖染料选择性地递送至视网膜细胞。重要的是,AuNP 给药或照射均不会导致 RGC 死亡。该系统提供了一种新颖的、非病毒的方法,有可能在保留健康区域的同时选择性地靶向病变区域的视网膜细胞,并且可能被用于未来针对视网膜退行性疾病的细胞特异性治疗。