Progressive lysosomal membrane permeabilization induced by iron oxide nanoparticles drives hepatic cell autophagy and apoptosis
Autor: | Barbora Smolková, Aleksey Nikitin, Igor Schetinin, Milan Jirsa, Mariia Uzhytchak, Valeria Rodionova, Stanislav Pshenichnikov, Alexandr Dejneka, D. G. Zhukov, Maxim A. Abakumov, Oleg Lunov, Alexander Omelyanchik, Alexander G. Savchenko, Mariia Lunova, Alexander G. Majouga, K. Levada |
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Rok vydání: | 2020 |
Předmět: |
Cytotoxicity
lcsh:Biotechnology Iron oxide Apoptosis 02 engineering and technology lcsh:Chemical technology lcsh:Technology Iron oxide nanoparticles 03 medical and health sciences chemistry.chemical_compound Magnetic resonance imaging lcsh:TP248.13-248.65 Autophagy lcsh:TP1-1185 General Materials Science lcsh:Science 030304 developmental biology 0303 health sciences Full Paper lcsh:T General Engineering 021001 nanoscience & nanotechnology lcsh:QC1-999 Cell biology chemistry Cell culture Toxicity Hepatic stellate cell lcsh:Q 0210 nano-technology lcsh:Physics |
Zdroj: | Nano Convergence, Vol 7, Iss 1, Pp 1-17 (2020) Nano Convergence |
ISSN: | 2196-5404 |
DOI: | 10.1186/s40580-020-00228-5 |
Popis: | Iron oxide nanoparticles (IONs) are frequently used in various biomedical applications, in particular as magnetic resonance imaging contrast agents in liver imaging. Indeed, number of IONs have been withdrawn due to their poor clinical performance. Yet comprehensive understanding of their interactions with hepatocytes remains relatively limited. Here we investigated how iron oxide nanocubes (IO-cubes) and clusters of nanocubes (IO-clusters) affect distinct human hepatic cell lines. The viability of HepG2, Huh7 and Alexander cells was concentration-dependently decreased after exposure to either IO-cubes or IO-clusters. We found similar cytotoxicity levels in three cell lines triggered by both nanoparticle formulations. Our data indicate that different expression levels of Bcl-2 predispose cell death signaling mediated by nanoparticles. Both nanoparticles induced rather apoptosis than autophagy in HepG2. Contrary, IO-cubes and IO-clusters trigger distinct cell death signaling events in Alexander and Huh7 cells. Our data clarifies the mechanism by which cubic nanoparticles induce autophagic flux and the mechanism of subsequent toxicity. These findings imply that the cytotoxicity of ION-based contrast agents should be carefully considered, particularly in patients with liver diseases. |
Databáze: | OpenAIRE |
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