King Jessica J, Chen Kai, Evans Cameron W, Norret Marck, Almasri Ruba, Pavlos Nathan J, Hui Henry Yl, Lin Qiongxiang, Bhatt Uditi, Young Stephen G, Smith Nicole M, Nikan Mehran, Prestidge Clive A, Jiang Haibo, Iyer K Swaminathan
School of Molecular Sciences, The University of Western Australia Perth WA 6009 Australia
ARC Training Centre for Next-Generation Biomedical Analysis, The University of Western Australia Perth WA 6009 Australia.
Chem Sci. 2024 Aug 28;15(38):15690-7. doi: 10.1039/d3sc06773d.
Antisense oligonucleotides (ASOs) are a well-established therapeutic modality based on RNA interference, but low cellular uptake, limited ability to direct ASO trafficking, and a range of intracellular barriers to successful activity compromise both gene silencing outcomes and clinical translations. Herein, we demonstrate that polymers can increase ASO internalisation intracellular trafficking pathways that are distinct from lipid-based delivery reagents. For the first time, we spatially define internalisation and dissociation stages in the polymer-mediated cytosolic delivery of ASOs using Nanoscale Secondary Ion Mass Spectrometry (NanoSIMS), which enables visualisation of ASO localisation at the organelle level. We find that polymer-ASO complexes are imported into cells, from which free ASO enters the cytosol following complex dissociation. This information enables a better understanding of the intracellular trafficking pathways of nucleic acid therapeutics and may be exploited for therapeutic delivery to enhance the effectiveness of nucleic acid therapeutics in the future.
反义寡核苷酸(ASO)是一种基于RNA干扰的成熟治疗方式,但细胞摄取率低、引导ASO运输的能力有限以及一系列影响成功发挥作用的细胞内障碍,均会损害基因沉默效果和临床转化。在此,我们证明聚合物可以增加ASO内化,其细胞内运输途径不同于基于脂质的递送试剂。我们首次使用纳米二次离子质谱(NanoSIMS)在空间上定义了聚合物介导的ASO胞质递送中的内化和解离阶段,这使得能够在细胞器水平可视化ASO定位。我们发现聚合物-ASO复合物被导入细胞,复合物解离后游离的ASO进入细胞质。这些信息有助于更好地理解核酸治疗药物的细胞内运输途径,并可能在未来用于治疗性递送,以提高核酸治疗药物的有效性。