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Updated: Jun 29, 2026

Identification of Metal Oxide Nanoparticles in Histological Samples by Enhanced Darkfield Microscopy and Hyperspectral Mapping
Published on: December 8, 2015
Elemental and molecular imaging of human full thickness skin after exposure to heavy metals
Laurent Chavatte1, Milène Juan2, Sandra Mounicou3
1Université de Pau et des Pays de l'Adour, E2S UPPA, CNRS, Institut des Sciences Analytiques et de Physico-Chimie Pour l'Environnement et les Materiaux (IPREM), UMR5254, Hélioparc, 64053 Pau, France and CIRI, Centre International de Recherche en Infectiologie, CIRI, 69007 Lyon, France and Institut National de la Santé et de la Recherche Médicale (INSERM) Unité U1111, 69007 Lyon, France and Ecole Normale Supérieure de Lyon, 69007 Lyon, France and Université Claude Bernard Lyon 1 (UCBL1), 69622 Lyon, France and Unité Mixte de Recherche 5308 (UMR5308), Centre national de la recherche scientifique (CNRS), 69007 Lyon, France.
Abstract:
Compelling evidence suggests that heavy metals have potentially harmful effects on the skin. However, knowledge about cellular signaling events and toxicity subsequent to human skin cell exposure to metals is still poorly documented. The aim of this study was to focus on the interaction between four different heavy metals (lead, nickel, cadmium, and mercury) at doses mimicking chronic low-levels of environmental exposure and the effect on skin to get better insight into metal-cell interactions. We provide evidence that the two metals (lead and nickel) can permeate the skin and accumulate at high concentrations in the dermis. The skin barrier was disrupted after metal exposure and this was accompanied by apoptosis, DNA damage and lipid oxidation. Skin antioxidant enzymes such as glutathione peroxidase and methionine sulfoxide reductase are also heavy metal targets. Taken together, our findings provide insight into potential mechanisms of metal-induced oxidative stress production and the cellular consequences of these events.
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