| Literature DB >> 30884043 |
Zhaoma Shu1, Iku Tanaka1, Azumi Ota1, Daichi Fushihara1, Naoko Abe1, Saki Kawaguchi1, Kosuke Nakamoto1, Fumiaki Tomoike2, Seiichi Tada3, Yoshihiro Ito3, Yasuaki Kimura1, Hiroshi Abe1,3,4.
Abstract
Development of intracellular delivery methods for antisense DNA and siRNA is important. Previously reported methods using liposomes or receptor-ligands take several hours or more to deliver oligonucleotides to the cytoplasm due to their retention in endosomes. Oligonucleotides modified with low molecular weight disulfide units at a terminus reach the cytoplasm 10 minutes after administration to cultured cells. This rapid cytoplasmic internalization of disulfide-modified oligonucleotides suggests the existence of an uptake pathway other than endocytosis. Mechanistic analysis revealed that the modified oligonucleotides are efficiently internalized into the cytoplasm through disulfide exchange reactions with the thiol groups on the cellular surface. This approach solves several critical problems with the currently available methods for enhancing cellular uptake of oligonucleotides and may be an effective approach in the medicinal application of antisense DNA and siRNA.Entities:
Keywords: antisense; cellular uptake; cytosolic delivery; disulfide; siRNA
Year: 2019 PMID: 30884043 DOI: 10.1002/anie.201900993
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336