TY - JOUR
T1 - Nanoparticles can cause DNA damage across a cellular barrier
AU - Bhabra, Gevdeep
AU - Sood, Aman
AU - Fisher, Brenton
AU - Cartwright, Laura
AU - Saunders, Margaret
AU - Evans, William Howard
AU - Surprenant, Annmarie
AU - Lopez-Castejon, Gloria
AU - Mann, Stephen
AU - Davis, Sean A.
AU - Hails, Lauren A.
AU - Ingham, Eileen
AU - Verkade, Paul
AU - Lane, Jon
AU - Heesom, Kate
AU - Newson, Roger
AU - Case, Charles Patrick
PY - 2009/12
Y1 - 2009/12
N2 - The increasing use of nanoparticles in medicine has raised concerns over their ability to gain access to privileged sites in the body. Here, we show that cobalt-chromium nanoparticles (29.5 6.3nm in diameter) can damage human fibroblast cells across an intact cellular barrier without having to cross the barrier. The damage is mediated by a novel mechanism involving transmission of purine nucleotides (such as ATP) and intercellular signalling within the barrier through connexin gap junctions or hemichannels and pannexin channels. The outcome, which includes DNA damage without significant cell death, is different from that observed in cells subjected to direct exposure to nanoparticles. Our results suggest the importance of indirect effects when evaluating the safety of nanoparticles. The potential damage to tissues located behind cellular barriers needs to be considered when using nanoparticles for targeting diseased states.
AB - The increasing use of nanoparticles in medicine has raised concerns over their ability to gain access to privileged sites in the body. Here, we show that cobalt-chromium nanoparticles (29.5 6.3nm in diameter) can damage human fibroblast cells across an intact cellular barrier without having to cross the barrier. The damage is mediated by a novel mechanism involving transmission of purine nucleotides (such as ATP) and intercellular signalling within the barrier through connexin gap junctions or hemichannels and pannexin channels. The outcome, which includes DNA damage without significant cell death, is different from that observed in cells subjected to direct exposure to nanoparticles. Our results suggest the importance of indirect effects when evaluating the safety of nanoparticles. The potential damage to tissues located behind cellular barriers needs to be considered when using nanoparticles for targeting diseased states.
U2 - 10.1038/nnano.2009.313
DO - 10.1038/nnano.2009.313
M3 - Article
C2 - 19893513
SN - 1748-3387
VL - 4
SP - 876
EP - 883
JO - Nature Nanotechnology
JF - Nature Nanotechnology
IS - 12
ER -