Department of Pharmacy, College of Pharmacy, CHA University, Seongnam 463-836, Republic of Korea.
J Biotechnol. 2011 Sep 20;155(3):287-92. doi: 10.1016/j.jbiotec.2011.07.014. Epub 2011 Jul 22.
MicroRNAs (miRNAs) are gaining recognition as essential regulators involved in many biological processes, and they are emerging as therapeutic targets for treating disease. Here, we introduce a method for effective delivery of anti-miRNA oligonucleotides (AMOs) using functionalized gold nanoparticles (AuNPs). To demonstrate the ability of AMOs to silence miRNA, we selected miR-29b, which is known to downregulate myeloid cell leukemia-1 (MCL-1), a factor responsible for promoting cell survival. We first generated AuNPs coated with cargo DNA, which was then coupled to complementary DNA linked to an antisense miR-29b sequence. When the AuNPs were delivered into HeLa cells, MCL-1 protein and mRNA levels were increased significantly. Furthermore, apoptosis induced by tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) was inhibited, proving that AMOs targeting miR-29b were effectively delivered by our innovative AuNP. In addition, we provided evidence that AuNP could deliver other AMOs against miR-21 into two independent cell lines, KGN and 293T, suggesting that the AuNP conjugates can be versatile for any AMO and cell type.
微小 RNA(miRNAs)作为参与许多生物过程的重要调控因子而受到关注,并且它们正成为治疗疾病的治疗靶点。在这里,我们介绍了一种使用功能化金纳米粒子(AuNPs)有效递送抗 miRNA 寡核苷酸(AMOs)的方法。为了证明 AMOs 沉默 miRNA 的能力,我们选择了 miR-29b,已知它下调髓样细胞白血病-1(MCL-1),这是一种负责促进细胞存活的因子。我们首先生成了负载有货物 DNA 的 AuNPs,然后将其与互补 DNA 偶联,互补 DNA 与抗 miR-29b 序列相连。当 AuNPs 被递送到 HeLa 细胞中时,MCL-1 蛋白和 mRNA 水平显著增加。此外,肿瘤坏死因子相关凋亡诱导配体(TRAIL)诱导的细胞凋亡被抑制,证明我们的创新 AuNP 有效地递送了靶向 miR-29b 的 AMOs。此外,我们提供了证据表明,AuNP 可以将其他针对 miR-21 的 AMOs 递送到两个独立的细胞系 KGN 和 293T 中,这表明 AuNP 缀合物可以针对任何 AMO 和细胞类型具有多功能性。