Elemental and molecular imaging of human full thickness skin after exposure to heavy metals
Author(s) -
Laurent Chavatte,
Milène Juan,
Sandra Mounicou,
Emmanuelle Noblesse,
Karl Pays,
Carine Nizard,
AnneLaure Bulteau
Publication year - 2020
Publication title -
metallomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.012
H-Index - 75
eISSN - 1756-591X
pISSN - 1756-5901
DOI - 10.1039/d0mt00121j
Subject(s) - dermis , oxidative stress , metal poisoning , chemistry , cadmium , metal toxicity , heavy metals , metal , skin aging , human skin , mercury (programming language) , glutathione peroxidase , dna damage , glutathione , biophysics , biochemistry , environmental chemistry , enzyme , dna , superoxide dismutase , biology , dermatology , anatomy , medicine , organic chemistry , genetics , computer science , programming language
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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