Specific Delivery of Oligonucleotides to the Cell Nucleus via Gentle Compression and Attachment of Polythymidine

• Published in: ACS applied materials & interfaces Vol. 11; no. 31; pp. 27624 - 27640
• Main Authors: Chen, Zhong, Li, Huize, Zhang, Lei, Lee, Carrie K, Ho, Lok Wai Cola, Chan, Cecilia Ka Wing, Yang, Hongrong, Choi, Chung Hang Jonathan
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 07-08-2019
• Subjects: Animals; Cell Nucleus - metabolism; Drug Delivery Systems; Mice; Oligodeoxyribonucleotides, Antisense - chemistry; Oligodeoxyribonucleotides, Antisense - pharmacokinetics; Oligodeoxyribonucleotides, Antisense - pharmacology; Poly T - chemistry; Poly T - pharmacokinetics; Poly T - pharmacology; RAW 264.7 Cells; specific delivery; polythymidine; cell nucleus; importin β; oligonucleotides; compression
• ISSN: 1944-8244; 1944-8252
• DOI: 10.1021/acsami.9b11391

Nonviral delivery of nucleic acids to the cell nucleus typically requires chemical methods that do not guarantee specific delivery (e.g., transfection agent) or physical methods that may require extensive fabrication (e.g., microfluidics) or an elevated pressure (e.g., 105 Pa for microneedles). We report a method of delivering oligonucleotides to the nucleus with high specificity (relative to the cytosol) by synergistically combining chemical and physical approaches. Particularly, we demonstrate that DNA oligonucleotides appended with a polythymidine [poly­(T)] segment (chemical) profusely accumulate inside the nucleus when the cells are under gentle compression imposed by the weight of a single glass coverslip (physical; ∼2.2 Pa). Our “compression-cum-poly­(T)” delivery method is simple, can be generalizable to three “hard-to-transfect” cell types, and does not induce significant levels of cytotoxicity or long-term oxidative stress to the treated cells when provided the use of suitable compression times and oligonucleotide concentrations. In bEnd.3 endothelial cells, compression-aided intranuclear delivery of poly­(T) is primarily mediated by importin β and nucleoporin 62. Our method significantly enhances the intranuclear delivery of antisense oligonucleotides to bEnd.3 endothelioma cells and the inhibition of two target genes, including a reporter gene encoding the enhanced green fluorescent protein and an intranuclear lncRNA oncogene (metastasis-associated lung adenocarcinoma transcript 1), when compared with delivery without gentle compression or poly­(T) attachment. Our data underscore the critical roles of pressure and nucleotide sequence on the intranuclear delivery of nucleic acids.