| Literature DB >> 19685445 |
Yvonne Williams1, Alyona Sukhanova, Małgorzata Nowostawska, Anthony M Davies, Siobhan Mitchell, Vladimir Oleinikov, Yurii Gun'ko, Igor Nabiev, Dermot Kelleher, Yuri Volkov.
Abstract
The compartmentalization of size-tuned luminescent semiconductor nanocrystal quantum dots (QDs) in four distinctive cell lines, which would be representative of the most likely environmental exposure routes to nanoparticles in humans, is studied. The cells are fixed and permeabilized prior to the addition of the QDs, thus eliminating any cell-membrane-associated effects due to active QD uptake mechanisms or to specificity of signaling routes in different cell types, but leaving intact the putative physical subcellular barriers. All quantitative assays are performed using a high content analysis (HCA) platform, thereby obtaining robust data on large cell populations. While smaller QDs 2.1 nm in diameter enter the nuclei and localize to the nucleoli in all cell types, the rate and dynamics of their passage vary depending on the cell origin. As the QD size is increased to 4.4 nm, penetration into the cell is reduced but each cell line displays its own cutoff size thresholds reflecting cell-type-determined cytoplasmic and nuclear pore penetration specificity. These results give rise to important considerations regarding the differential compartmentalization and susceptibility of organs, tissues, and cells to nanoparticles, and may be of prime importance for biomedical imaging and drug-delivery research employing nanoparticle-based probes and systems.Entities:
Mesh:
Year: 2009 PMID: 19685445 DOI: 10.1002/smll.200900744
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281