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The impact of species and cell type on the nanosafety profile of iron oxide nanoparticles in neural cells

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Abstract
Background: While nanotechnology is advancing rapidly, nanosafety tends to lag behind since general mechanistic insights into cell-nanoparticle (NP) interactions remain rare. To tackle this issue, standardization of nanosafety assessment is imperative. In this regard, we believe that the cell type selection should not be overlooked since the applicability of cell lines could be questioned given their altered phenotype. Hence, we evaluated the impact of the cell type on in vitro nanosafety evaluations in a human and murine neuroblastoma cell line, neural progenitor cell line and in neural stem cells. Acute toxicity was evaluated for gold, silver and iron oxide (IO) NPs, and the latter were additionally subjected to a multiparametric analysis to assess sublethal effects. Results: The stem cells and murine neuroblastoma cell line respectively showed most and least acute cytotoxicity. Using high content imaging, we observed cell type-and species-specific responses to the IONPs on the level of reactive oxygen species production, calcium homeostasis, mitochondrial integrity and cell morphology, indicating that cellular homeostasis is impaired in distinct ways. Conclusions: Our data reveal cell type-specific toxicity profiles and demonstrate that a single cell line or toxicity end point will not provide sufficient information on in vitro nanosafety. We propose to identify a set of standard cell lines for screening purposes and to select cell types for detailed nanosafety studies based on the intended application and/or expected exposure.
Keywords
Multiparametric analysis, IN-VITRO CYTOTOXICITY, OXIDATIVE STRESS, SILVER NANOPARTICLES, Stem cells, Iron oxide nanoparticles, Inorganic nanoparticles, Nanosafety, High content imaging, MITOCHONDRIAL ACTIVITY, GENE-EXPRESSION, DOSE-RESPONSE, LINES, STEM, TOXICITY, CALCIUM

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MLA
Joris, Freya, et al. “The Impact of Species and Cell Type on the Nanosafety Profile of Iron Oxide Nanoparticles in Neural Cells.” JOURNAL OF NANOBIOTECHNOLOGY, vol. 14, 2016, doi:10.1186/s12951-016-0220-y.
APA
Joris, F., Valdepérez, D., Pelaz, B., Soenen, S. J., Manshian, B. B., Parak, W. J., … Raemdonck, K. (2016). The impact of species and cell type on the nanosafety profile of iron oxide nanoparticles in neural cells. JOURNAL OF NANOBIOTECHNOLOGY, 14. https://doi.org/10.1186/s12951-016-0220-y
Chicago author-date
Joris, Freya, Daniel Valdepérez, Beatriz Pelaz, Stefaan J Soenen, Bella B Manshian, Wolfgang J Parak, Stefaan De Smedt, and Koen Raemdonck. 2016. “The Impact of Species and Cell Type on the Nanosafety Profile of Iron Oxide Nanoparticles in Neural Cells.” JOURNAL OF NANOBIOTECHNOLOGY 14. https://doi.org/10.1186/s12951-016-0220-y.
Chicago author-date (all authors)
Joris, Freya, Daniel Valdepérez, Beatriz Pelaz, Stefaan J Soenen, Bella B Manshian, Wolfgang J Parak, Stefaan De Smedt, and Koen Raemdonck. 2016. “The Impact of Species and Cell Type on the Nanosafety Profile of Iron Oxide Nanoparticles in Neural Cells.” JOURNAL OF NANOBIOTECHNOLOGY 14. doi:10.1186/s12951-016-0220-y.
Vancouver
1.
Joris F, Valdepérez D, Pelaz B, Soenen SJ, Manshian BB, Parak WJ, et al. The impact of species and cell type on the nanosafety profile of iron oxide nanoparticles in neural cells. JOURNAL OF NANOBIOTECHNOLOGY. 2016;14.
IEEE
[1]
F. Joris et al., “The impact of species and cell type on the nanosafety profile of iron oxide nanoparticles in neural cells,” JOURNAL OF NANOBIOTECHNOLOGY, vol. 14, 2016.
@article{8133095,
  abstract     = {{Background: While nanotechnology is advancing rapidly, nanosafety tends to lag behind since general mechanistic insights into cell-nanoparticle (NP) interactions remain rare. To tackle this issue, standardization of nanosafety assessment is imperative. In this regard, we believe that the cell type selection should not be overlooked since the applicability of cell lines could be questioned given their altered phenotype. Hence, we evaluated the impact of the cell type on in vitro nanosafety evaluations in a human and murine neuroblastoma cell line, neural progenitor cell line and in neural stem cells. Acute toxicity was evaluated for gold, silver and iron oxide (IO) NPs, and the latter were additionally subjected to a multiparametric analysis to assess sublethal effects. 
Results: The stem cells and murine neuroblastoma cell line respectively showed most and least acute cytotoxicity. Using high content imaging, we observed cell type-and species-specific responses to the IONPs on the level of reactive oxygen species production, calcium homeostasis, mitochondrial integrity and cell morphology, indicating that cellular homeostasis is impaired in distinct ways. 
Conclusions: Our data reveal cell type-specific toxicity profiles and demonstrate that a single cell line or toxicity end point will not provide sufficient information on in vitro nanosafety. We propose to identify a set of standard cell lines for screening purposes and to select cell types for detailed nanosafety studies based on the intended application and/or expected exposure.}},
  articleno    = {{69}},
  author       = {{Joris, Freya and Valdepérez, Daniel and Pelaz, Beatriz and Soenen, Stefaan J and Manshian, Bella B and Parak, Wolfgang J and De Smedt, Stefaan and Raemdonck, Koen}},
  issn         = {{1477-3155}},
  journal      = {{JOURNAL OF NANOBIOTECHNOLOGY}},
  keywords     = {{Multiparametric analysis,IN-VITRO CYTOTOXICITY,OXIDATIVE STRESS,SILVER NANOPARTICLES,Stem cells,Iron oxide nanoparticles,Inorganic nanoparticles,Nanosafety,High content imaging,MITOCHONDRIAL ACTIVITY,GENE-EXPRESSION,DOSE-RESPONSE,LINES,STEM,TOXICITY,CALCIUM}},
  language     = {{eng}},
  pages        = {{13}},
  title        = {{The impact of species and cell type on the nanosafety profile of iron oxide nanoparticles in neural cells}},
  url          = {{http://doi.org/10.1186/s12951-016-0220-y}},
  volume       = {{14}},
  year         = {{2016}},
}

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