Visualization of silver nanoparticle intracellular trafficking revealed nuclear translocation of silver ions leading to nuclear receptor impairment
Abstract The impact on human health of the increasing use of silver nanoparticles (AgNPs) in medical devices remains understudied, even though AgNP-containing dressings are known to release silver in the bloodstream leading to accumulation and slow clearance in the liver. Cellular studies have shown the intracellular dissolution of AgNPs within endo-lysosomes followed by Ag(I) binding to biomolecular thiolate-containing molecules. However, the precise subcellular distribution of Ag(I) and the nature of the disrupted physiological pathways remained unknown. Novel imaging approaches enabled us to visualize the trafficking of AgNP-containing lysosomes towards a perinuclear location and a direct nuclear transfer of Ag(I) species with accumulation in the nucleoli. These Ag(I) species impaired nuclear receptor activity, disrupting critical mechanisms of liver physiology in very low dose exposure scenarios, thus justifying further research into defining a framework for the safe use of AgNPs..
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Preprint| Erscheinungsjahr: |
2021 |
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| Erschienen: |
2021 |
| Enthalten in: |
bioRxiv.org - (2021) vom: 26. Jan. Zur Gesamtaufnahme - year:2021 |
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| Sprache: |
Englisch |
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| Beteiligte Personen: |
Suárez, Vanessa Tardillo [VerfasserIn] |
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| Links: |
Volltext [kostenfrei] |
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| doi: |
10.1101/825919 |
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| PPN (Katalog-ID): |
XBI000659908 |
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| 245 | 1 | 0 | |a Visualization of silver nanoparticle intracellular trafficking revealed nuclear translocation of silver ions leading to nuclear receptor impairment |
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| 520 | |a Abstract The impact on human health of the increasing use of silver nanoparticles (AgNPs) in medical devices remains understudied, even though AgNP-containing dressings are known to release silver in the bloodstream leading to accumulation and slow clearance in the liver. Cellular studies have shown the intracellular dissolution of AgNPs within endo-lysosomes followed by Ag(I) binding to biomolecular thiolate-containing molecules. However, the precise subcellular distribution of Ag(I) and the nature of the disrupted physiological pathways remained unknown. Novel imaging approaches enabled us to visualize the trafficking of AgNP-containing lysosomes towards a perinuclear location and a direct nuclear transfer of Ag(I) species with accumulation in the nucleoli. These Ag(I) species impaired nuclear receptor activity, disrupting critical mechanisms of liver physiology in very low dose exposure scenarios, thus justifying further research into defining a framework for the safe use of AgNPs. | ||
| 700 | 1 | |a Karepina, Elizaveta |e verfasserin |4 aut | |
| 700 | 1 | |a Chevallet, Mireille |e verfasserin |4 aut | |
| 700 | 1 | |a Gallet, Benoit |e verfasserin |4 aut | |
| 700 | 1 | |a Cottet-Rousselle, Cécile |e verfasserin |4 aut | |
| 700 | 1 | |a Charbonnier, Peggy |e verfasserin |4 aut | |
| 700 | 1 | |a Moriscot, Christine |e verfasserin |4 aut | |
| 700 | 1 | |a Michaud-Soret, Isabelle |e verfasserin |4 aut | |
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