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三维细胞培养中的超顺磁纳米粒子基因传递。

Gene delivery in three-dimensional cell cultures by superparamagnetic nanoparticles.

机构信息

Department of Chemical and Biological Engineering and Center for Biotechnology and Interdisciplinary Science, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.

出版信息

ACS Nano. 2010 Aug 24;4(8):4733-43. doi: 10.1021/nn9018812.

Abstract

Three-dimensional (3D) cellular assays closely mimic the in vivo milieu, providing a rapid, inexpensive system for screening drug candidates for toxicity or efficacy in the early stages of drug discovery. However, 3D culture systems may suffer from mass transfer limitations, particularly in delivery of large polypeptide or nucleic acid compounds. Nucleic acids (e.g., genes, silencing RNA) are of particular interest both as potential therapeutics and due to a desire to modulate the gene-expression patterns of cells exposed to small-molecule pharmacological agents. In the present study, polyethylenimine (PEI)-coated superparamagnetic nanoparticles (SPMNs) were designed to deliver interfering RNA and green fluorescent protein (GFP) plasmids through a collagen-gel matrix into 3D cell cultures driven by an external magnetic field. The highest transfection efficiency achieved was 64% for siRNA and 77% for GFP plasmids. Delivery of an shRNA plasmid against GFP by PEI-coated SPMNs silenced the GFP expression with 82% efficiency. We further demonstrated that this delivery approach could be used for screening interfering RNA constructs for therapeutic or toxic effects for cells grown in 3D cultures. Four known toxic shRNA plasmids were delivered by PEI-coated SPMNs into 3D cell cultures, and significant toxicities (41-51% cell death) were obtained.

摘要

三维(3D)细胞检测法与体内环境密切相似,为在药物发现的早期阶段筛选候选药物的毒性或疗效提供了一种快速、廉价的系统。然而,3D 培养系统可能会受到传质限制,特别是在输送大型多肽或核酸化合物时。核酸(例如基因、沉默 RNA)不仅作为潜在的治疗剂,而且由于希望调节暴露于小分子药理学制剂的细胞的基因表达模式,因此特别感兴趣。在本研究中,设计了聚乙烯亚胺(PEI)涂层超顺磁性纳米颗粒(SPMN),通过外部磁场将干扰 RNA 和绿色荧光蛋白(GFP)质粒递送至胶原凝胶基质中的 3D 细胞培养物中。获得的最高转染效率为 siRNA 的 64%和 GFP 质粒的 77%。PEI 涂层 SPMN 递送针对 GFP 的 shRNA 质粒可有效沉默 GFP 表达,效率为 82%。我们进一步证明,这种递药方法可用于筛选用于 3D 培养细胞的治疗或毒性作用的干扰 RNA 构建体。将四个已知的毒性 shRNA 质粒通过 PEI 涂层 SPMN 递送至 3D 细胞培养物中,获得了显著的毒性(41-51%的细胞死亡)。

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