Department of Chemistry, National Taiwan University , Taipei 106, Taiwan.
Mackay Junior College of Medicine , Nursing and Management, Taipei 112, Taiwan.
ACS Appl Mater Interfaces. 2016 Jul 20;8(28):17944-54. doi: 10.1021/acsami.6b05834. Epub 2016 Jul 11.
Reactive oxygen species (ROS) are important factors in many clinical diseases. However, direct delivery of antioxidant enzymes into cells is difficult due to poor cell uptake. A proper design of delivery of enzymes by nanoparticles is very desirable for therapeutic purposes. To overcome the cell barrier problem, a designed mesoporous silica nanoparticle (MSN) system with attached TAT-fusion denatured enzyme for enhancing cell membrane penetration has been developed. Simultaneous delivery of two up-downstream antioxidant enzymes, superoxide dismutase (SOD) and glutathione peroxidase(GPx), reveals synergistic efficiency of ROS scavenging, compared to single antioxidant enzyme delivery. TAT peptide conjugation provided a facile nonendocytosis cell uptake and escape from endosome while moving and aggregating along the cytoskeleton that would allow them to be close to each other at the same time, resulting in the cellular antioxidation cascade reaction. The two-enzyme delivery shows a significant synergistic effect for protecting cells against ROS-induced cell damage and cell cycle arrest. The nanocarrier strategy for enzyme delivery demonstrates that intracellular anti-ROS cascade reactions could be regulated by multifunctional MSNs carrying image fluorophore and relevant antioxidation enzymes.
活性氧(ROS)是许多临床疾病的重要因素。然而,由于细胞摄取能力差,将抗氧化酶直接递送到细胞中是很困难的。因此,非常需要通过纳米粒子来设计酶的递送来达到治疗的目的。为了克服细胞屏障问题,设计了一种具有附着 TAT-融合变性酶的介孔硅纳米粒子(MSN)系统,以增强细胞膜穿透性。同时递送两种上下游抗氧化酶,超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx),与单一抗氧化酶递呈相比,揭示了 ROS 清除的协同效率。TAT 肽缀合提供了一种简便的非内吞细胞摄取,并从内涵体逃逸,同时沿着细胞骨架移动和聚集,从而使它们能够同时彼此靠近,导致细胞内抗氧化级联反应。两种酶的递呈显示出对 ROS 诱导的细胞损伤和细胞周期阻滞有显著的协同保护作用。该酶递呈的纳米载体策略表明,通过携带荧光团和相关抗氧化酶的多功能 MSN 可以调节细胞内抗 ROS 级联反应。