| Literature DB >> 30297819 |
Diwei Ho1, Jessica A Kretzmann1, Marck Norret1, Priyanka Toshniwal1, Jean-Pierre Veder2, Haibo Jiang1,3, Paul Guagliardo3, Alaa M Munshi1,4, Reena Chawla5,6,7, Cameron W Evans1, Tristan D Clemons1, Michelle Nguyen1, Amy L Kretzmann1, Amanda J Blythe1, Martin Saunders1,3, Michael Archer8, Melinda Fitzgerald8,9,10, Jeffrey A Keelan11, Charles S Bond1, Matt R Kilburn3, Laurence H Hurley5,6,7, Nicole M Smith12, K Swaminathan Iyer13.
Abstract
Gold nanorods are one of the most widely explored inorganic materials in nanomedicine for diagnostics, therapeutics and sensing1. It has been shown that gold nanorods are not cytotoxic and localize within cytoplasmic vesicles following endocytosis, with no nuclear localization2,3, but other studies have reported alterations in gene expression profiles in cells following exposure to gold nanorods, via unknown mechanisms4. In this work we describe a pathway that can contribute to this phenomenon. By mapping the intracellular chemical speciation process of gold nanorods, we show that the commonly used Au-thiol conjugation, which is important for maintaining the noble (inert) properties of gold nanostructures, is altered following endocytosis, resulting in the formation of Au(I)-thiolates that localize in the nucleus5. Furthermore, we show that nuclear localization of the gold species perturbs the dynamic microenvironment within the nucleus and triggers alteration of gene expression in human cells. We demonstrate this using quantitative visualization of ubiquitous DNA G-quadruplex structures, which are sensitive to ionic imbalances, as an indicator of the formation of structural alterations in genomic DNA.Entities:
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Year: 2018 PMID: 30297819 DOI: 10.1038/s41565-018-0272-2
Source DB: PubMed Journal: Nat Nanotechnol ISSN: 1748-3387 Impact factor: 39.213