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Uptake efficiency of surface modified gold nanoparticles does not correlate with functional changes and cytokine secretion in human dendritic cells in vitro
Type of publication
Peer-reviewed
Publikationsform
Original article (peer-reviewed)
Author
Fytianos Kleanthis, Rodriguez-Lorenzo Laura, Clift Martin J. D., Blank Fabian, Vanhecke Dimitri, von Garnier Christophe, Petri-Fink Alke, Rothen-Rutishauser Barbara,
Project
Biomedical nanoparticles as immune-modulators
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Original article (peer-reviewed)
Journal
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE
Volume (Issue)
11(3)
Page(s)
633 - 644
Title of proceedings
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE
DOI
10.1016/j.nano.2014.11.004
Abstract
Engineering nanoparticles (NPs) for immune modulation require a thorough understanding of their interaction(s) with cells. Gold NPs (AuNPs) were coated with polyethylene glycol (PEG), polyvinyl alcohol (PVA) or a mixture of both with either positive or negative surface charge to investigate uptake and cell response in monocyte-derived dendritic cells (MDDCs). Inductively coupled plasma optical emission spectrometry and transmission electron microscopy were used to confirm the presence of Au inside MDDCs. Cell viability, (pro-)inflammatory responses, MDDC phenotype, activation markers, antigen uptake and processing were analyzed. Cell death was only observed for PVA-NH2 AuNPs at the highest concentration. MDDCs internalize AuNPs, however, surface modification influenced uptake. Though limited uptake was observed for PEG-COOH AuNPs, a significant tumor necrosis factor-alpha release was induced. In contrast, (PEG+PVA)-NH2 and PVA-NH2 AuNPs were internalized to a higher extent and caused interleukin-1beta secretion. None of the AuNPs caused changes in MDDC phenotype, activation or immunological properties. From the clinical editor: This team of authors investigated the influence of gold nano-particles with different surface modifications on immunological properties in monocyte-derived dendritic cells. AuNPs triggered responses in these cells that has to be further investigated in terms of development of novel vaccine carriers
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