Size-dependent effects of gold nanoparticles uptake on maturation and antitumor functions of human dendritic cells in vitro

Autor: Srđa Janković, Dragana Vučević, Bernd Friedrich, Jelena Rajković, Sergej Tomić, Miodrag Čolić, Nina Ogrinc, Marjan Slak Rupnik, Sasa Vasilijic, Petar Milosavljevic, Rebeka Rudolf, Primož Pelicon, Ivan Anžel, Jelena Đokić
Jazyk: angličtina
Rok vydání: 2014
Předmět:
Lipopolysaccharides
T-Lymphocytes
lcsh:Medicine
02 engineering and technology
law.invention
Analytical Chemistry
Spectrum Analysis Techniques
Cell Signaling
law
Animal Cells
Molecular Cell Biology
Medicine
Nanotechnology
lcsh:Science
Cells
Cultured

0303 health sciences
Multidisciplinary
medicine.diagnostic_test
Size dependent
Cell Polarity
021001 nanoscience & nanotechnology
Flow Cytometry
Interleukin-12
3. Good health
Cell biology
Chemistry
Colloidal gold
Research Design
Spectrophotometry
Physical Sciences
Engineering and Technology
Cytophotometry
Cellular Types
0210 nano-technology
Research Article
Signal Transduction
Tumor Immunology
Immune Cells
Immunology
Materials Science
Antigen-Presenting Cells
Antineoplastic Agents
Research and Analysis Methods
Flow cytometry
03 medical and health sciences
Th2 Cells
Chemical Analysis
Confocal microscopy
Humans
Calcium Signaling
Particle Size
Materials by Attribute
030304 developmental biology
Nanomaterials
business.industry
lcsh:R
Quantitative Analysis
Biology and Life Sciences
Cell Biology
Dendritic Cells
In vitro
Apoptosis
Nanoparticles
Th17 Cells
Necrotic tumor
lcsh:Q
Gold
Electron microscope
business
Cytometry
T-Lymphocytes
Cytotoxic
Zdroj: PLoS ONE, Vol 9, Iss 5, p e96584 (2014)
PLOS ONE 9(5), e96584 (2014). doi:10.1371/journal.pone.0096584
PLoS ONE
ISSN: 1932-6203
Popis: Gold nanoparticles (GNPs) are claimed as outstanding biomedical tools for cancer diagnostics and photo-thermal therapy, but without enough evidence on their potentially adverse immunological effects. Using a model of human dendritic cells (DCs), we showed that 10 nm- and 50 nm-sized GNPs (GNP10 and GNP50, respectively) were internalized predominantly via dynamin-dependent mechanisms, and they both impaired LPS-induced maturation and allostimulatory capacity of DCs, although the effect of GNP10 was more prominent. However, GNP10 inhibited LPS-induced production of IL-12p70 by DCs, and potentiated their Th2 polarization capacity, while GNP50 promoted Th17 polarization. Such effects of GNP10 correlated with a stronger inhibition of LPS-induced changes in Ca2+ oscillations, their higher number per DC, and more frequent extra-endosomal localization, as judged by live-cell imaging, proton, and electron microscopy, respectively. Even when released from heat-killed necrotic HEp-2 cells, GNP10 inhibited the necrotic tumor cell-induced maturation and functions of DCs, potentiated their Th2/Th17 polarization capacity, and thus, impaired the DCs' capacity to induce T cell-mediated anti-tumor cytotoxicity in vitro. Therefore, GNP10 could potentially induce more adverse DC-mediated immunological effects, compared to GNP50.
Databáze: OpenAIRE