Department of Biomedical Science, College of Life Science, CHA University, 222 Yatap-Dong, Seongnam 463-836, South Korea.
Biomaterials. 2011 Apr;32(10):2593-604. doi: 10.1016/j.biomaterials.2010.11.074. Epub 2011 Jan 19.
The development of a method that can efficiently deliver nucleic acids into the nucleus of living systems remains one of the key challenges for experimental and therapeutic use of nonbiological gene delivery agents. In the current study, we demonstrate a functionalized gold nanoparticle (AuNP) that can serve as a universal carrier for the delivery of DNA oligonucleotides (oligos) into the nucleus. We designed various types of DNA oligos to redirect alternative splicing of pre-mRNAs, such as MCL-1 and BCL-6, and to sequester transcriptional factors, including estrogen receptor α and p53. We successfully delivered the oligos into the nucleus, resulting in the targeted effects. In addition, injection of the antisense DNAs into a xenograft tumor in a mouse model system resulted in inhibited development of the tumor by redirecting the alternative splicing of the pre-mRNA. Our findings show that these nanoconjugates efficiently load and deliver antisense DNAs to redirect gene splicing or double-stranded DNAs to decoy gene transcription by transcriptional factors into mammalian cells and in vivo animals. Therefore, our lego-like AuNP gene delivery system can be used universally to control different biological processes by modulating nuclear gene expression events in living systems.
开发一种能够将核酸高效递送至活体细胞细胞核内的方法仍然是生物非基因传递剂实验和治疗应用的关键挑战之一。在本研究中,我们展示了一种功能化的金纳米颗粒(AuNP),它可以作为将 DNA 寡核苷酸(oligos)递送至细胞核的通用载体。我们设计了各种类型的 DNA oligos 来重新定向前体 mRNA 的选择性剪接,如 MCL-1 和 BCL-6,并隔离转录因子,包括雌激素受体 α 和 p53。我们成功地将 oligos 递送至细胞核内,从而实现了靶向作用。此外,将反义 DNA 注射到小鼠模型系统的异种移植肿瘤中,通过重新定向前体 mRNA 的选择性剪接,抑制了肿瘤的发展。我们的研究结果表明,这些纳米复合物能够高效地装载和递送入核的反义 DNA,以通过转录因子重新定向基因剪接或双链 DNA 来诱捕基因转录,从而进入哺乳动物细胞和体内动物。因此,我们的积木式 AuNP 基因传递系统可以普遍用于通过调节活细胞内的核基因表达事件来控制不同的生物学过程。