Oxidative stress response in neural stem cells exposed to different superparamagnetic iron oxide nanoparticles
Language English Country New Zealand Media electronic-ecollection
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27217748
PubMed Central
PMC4853020
DOI
10.2147/ijn.s102730
PII: ijn-11-1701
Knihovny.cz E-resources
- Keywords
- biocompatibility, genotoxicity, murine neural stem cells, oxidative stress, superparamagnetic iron oxide nanoparticles,
- MeSH
- Antioxidants pharmacology MeSH
- Dextrans pharmacology MeSH
- Hydrodynamics MeSH
- Magnetite Nanoparticles MeSH
- Membrane Potentials drug effects MeSH
- Membrane Potential, Mitochondrial drug effects MeSH
- Mice, Inbred C57BL MeSH
- Nanoparticles chemistry ultrastructure MeSH
- Neural Stem Cells drug effects pathology MeSH
- Oxidative Stress drug effects MeSH
- DNA Damage MeSH
- Reactive Oxygen Species metabolism MeSH
- Static Electricity MeSH
- Cell Survival drug effects MeSH
- Ferric Compounds pharmacology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antioxidants MeSH
- Dextrans MeSH
- ferric oxide MeSH Browser
- ferumoxides MeSH Browser
- Magnetite Nanoparticles MeSH
- Reactive Oxygen Species MeSH
- Ferric Compounds MeSH
Biocompatibility, safety, and risk assessments of superparamagnetic iron oxide nanoparticles (SPIONs) are of the highest priority in researching their application in biomedicine. One improvement in the biological properties of SPIONs may be achieved by different functionalization and surface modifications. This study aims to investigate how a different surface functionalization of SPIONs - uncoated, coated with d-mannose, or coated with poly-l-lysine - affects biocompatibility. We sought to investigate murine neural stem cells (NSCs) as important model system for regenerative medicine. To reveal the possible mechanism of toxicity of SPIONs on NSCs, levels of reactive oxygen species, intracellular glutathione, mitochondrial membrane potential, cell-membrane potential, DNA damage, and activities of SOD and GPx were examined. Even in cases where reactive oxygen species levels were significantly lowered in NSCs exposed to SPIONs, we found depleted intracellular glutathione levels, altered activities of SOD and GPx, hyperpolarization of the mitochondrial membrane, dissipated cell-membrane potential, and increased DNA damage, irrespective of the surface coating applied for SPION stabilization. Although surface coating should prevent the toxic effects of SPIONs, our results showed that all of the tested SPION types affected the NSCs similarly, indicating that mitochondrial homeostasis is their major cellular target. Despite the claimed biomedical benefits of SPIONs, the refined determination of their effects on various cellular functions presented in this work highlights the need for further safety evaluations. This investigation helps to fill the knowledge gaps on the criteria that should be considered in evaluating the biocompatibility and safety of novel nanoparticles.
Institute for Medical Research and Occupational Health Zagreb Croatia
School of Medicine Croatian Institute for Brain Research University of Zagreb Zagreb Croatia
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