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Surface PEGylation suppresses pulmonary effects of CuO in allergen-induced lung inflammation.
Ilves, Marit; Kinaret, Pia Anneli Sofia; Ndika, Joseph; Karisola, Piia; Marwah, Veer; Fortino, Vittorio; Fedutik, Yuri; Correia, Manuel; Ehrlich, Nicky; Loeschner, Katrin; Besinis, Alexandros; Vassallo, Joanne; Handy, Richard D; Wolff, Henrik; Savolainen, Kai; Greco, Dario; Alenius, Harri.
Afiliación
  • Ilves M; Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, 00290, Helsinki, Finland.
  • Kinaret PAS; Institute of Biotechnology, University of Helsinki, 00790, Helsinki, Finland.
  • Ndika J; Faculty of Medicine and Life Sciences, University of Tampere, 33100, Tampere, Finland.
  • Karisola P; Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, 00290, Helsinki, Finland.
  • Marwah V; Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, 00290, Helsinki, Finland.
  • Fortino V; Institute of Biotechnology, University of Helsinki, 00790, Helsinki, Finland.
  • Fedutik Y; Faculty of Medicine and Life Sciences, University of Tampere, 33100, Tampere, Finland.
  • Correia M; Institute of Biotechnology, University of Helsinki, 00790, Helsinki, Finland.
  • Ehrlich N; Biomedicine Institute, University of Eastern Finland, 70211, Kuopio, Finland.
  • Loeschner K; PlasmaChem GmbH, 12489, Berlin, Germany.
  • Besinis A; National Food Institute, Technical University of Denmark, 2800, Lyngby, Denmark.
  • Vassallo J; Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800, Lyngby, Denmark.
  • Handy RD; National Food Institute, Technical University of Denmark, 2800, Lyngby, Denmark.
  • Wolff H; School of Biological and Marine Sciences, Faculty of Science and Engineering, University of Plymouth, Drake Circus, Plymouth, PL4 8AA, UK.
  • Savolainen K; Plymouth University Peninsula Schools of Medicine and Dentistry, University of Plymouth, John Bull Building, Tamar Science Park, Plymouth, PL6 8BU, UK.
  • Greco D; School of Biological and Marine Sciences, Faculty of Science and Engineering, University of Plymouth, Drake Circus, Plymouth, PL4 8AA, UK.
  • Alenius H; School of Biological and Marine Sciences, Faculty of Science and Engineering, University of Plymouth, Drake Circus, Plymouth, PL4 8AA, UK.
Part Fibre Toxicol ; 16(1): 28, 2019 07 05.
Article en En | MEDLINE | ID: mdl-31277695
ABSTRACT

BACKGROUND:

Copper oxide (CuO) nanomaterials are used in a wide range of industrial and commercial applications. These materials can be hazardous, especially if they are inhaled. As a result, the pulmonary effects of CuO nanomaterials have been studied in healthy subjects but limited knowledge exists today about their effects on lungs with allergic airway inflammation (AAI). The objective of this study was to investigate how pristine CuO modulates allergic lung inflammation and whether surface modifications can influence its reactivity. CuO and its carboxylated (CuO COOH), methylaminated (CuO NH3) and PEGylated (CuO PEG) derivatives were administered here on four consecutive days via oropharyngeal aspiration in a mouse model of AAI. Standard genome-wide gene expression profiling as well as conventional histopathological and immunological methods were used to investigate the modulatory effects of the nanomaterials on both healthy and compromised immune system.

RESULTS:

Our data demonstrates that although CuO materials did not considerably influence hallmarks of allergic airway inflammation, the materials exacerbated the existing lung inflammation by eliciting dramatic pulmonary neutrophilia. Transcriptomic analysis showed that CuO, CuO COOH and CuO NH3 commonly enriched neutrophil-related biological processes, especially in healthy mice. In sharp contrast, CuO PEG had a significantly lower potential in triggering changes in lungs of healthy and allergic mice revealing that surface PEGylation suppresses the effects triggered by the pristine material.

CONCLUSIONS:

CuO as well as its functionalized forms worsen allergic airway inflammation by causing neutrophilia in the lungs, however, our results also show that surface PEGylation can be a promising approach for inhibiting the effects of pristine CuO. Our study provides information for health and safety assessment of modified CuO materials, and it can be useful in the development of nanomedical applications.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neumonía / Polietilenglicoles / Cobre / Infiltración Neutrófila / Nanopartículas / Transcriptoma Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Part Fibre Toxicol Asunto de la revista: TOXICOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Finlandia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neumonía / Polietilenglicoles / Cobre / Infiltración Neutrófila / Nanopartículas / Transcriptoma Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Part Fibre Toxicol Asunto de la revista: TOXICOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Finlandia