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通过功能化金纳米粒子有效递送达 miRNA DNA 寡核苷酸。

Effective delivery of anti-miRNA DNA oligonucleotides by functionalized gold nanoparticles.

机构信息

Department of Pharmacy, College of Pharmacy, CHA University, Seongnam 463-836, Republic of Korea.

出版信息

J Biotechnol. 2011 Sep 20;155(3):287-92. doi: 10.1016/j.jbiotec.2011.07.014. Epub 2011 Jul 22.

Abstract

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.

摘要

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。

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