Characterization of the modes of action of deoxynivalenol (DON) in the human Jurkat T-cell line

Autor: Peter J.M. Hendriksen, Henk Van Loveren, Madhumohan R. Katika, Ad A. C. M. Peijnenburg
Přispěvatelé: GezondheidsRisico Analyse en Toxicologie, Toxicogenomics, RS: GROW - Oncology, RS: GROW - R1 - Prevention
Jazyk: angličtina
Rok vydání: 2015
Předmět:
endoplasmic-reticulum stress
vomitoxin deoxynivalenol
Novel Foods & Agrochains
T-Lymphocytes
deoxynivalenol
Apoptosis
Novel Foods & Agroketens
Lymphocyte Activation
Toxicology
Jurkat cells
chemistry.chemical_compound
Nuclear Receptor Subfamily 4
Group A
Member 1

oxidative stress
trichothecene deoxynivalenol
BU Toxicology
Novel Foods & Agrochains

activated protein-kinases
Kelch-Like ECH-Associated Protein 1
wheat products
Caspase 3
BU Toxicology
Intracellular Signaling Peptides and Proteins
NF-kappa B
NFAT
Ribosome Subunits
Large
Eukaryotic

kappa-b activation
Endoplasmic Reticulum Stress
Cell biology
Protein Transport
medicine.anatomical_structure
BU Toxicologie
Novel Foods & Agroketens

cytokine production
ER stress
Cell type
BU Toxicologie
NF-E2-Related Factor 2
T cell
Immunology
Biology
Immune system
transcription factors
medicine
Humans
Calcium Signaling
Activating Transcription Factor 3
immunotoxicity
NF-κB
induced apoptosis
gene-expression
chemistry
Unfolded protein response
Edible Grain
Trichothecenes
Biomarkers
Transcription Factor CHOP
Zdroj: Journal of Immunotoxicology 12 (2015) 3
Journal of Immunotoxicology, 12(3), 206-216. Informa Healthcare
Journal of Immunotoxicology, 12(3), 206-216
ISSN: 1547-691X
Popis: Deoxynivalenol (DON) is one of the most abundant mycotoxins worldwide and mostly detected in cereals and grains. As such, DON poses a risk for many adverse health effects to human and animals. In particular, immune cells are very sensitive to DON, with the initiating step leading to toxicity being a binding to the eukaryotic 60S ribosomal subunit and induction of ribotoxic stress. The present study aimed to: (1) extend insight into the mechanism of action (MOA) of DON in immune cells; and (2) understand why immune cells are more sensitive to DON than most other cell types. Previously published microarray studies have described the effects of DON on immune cells. To build upon these findings, here, immunocytological and biochemical studies were performed using human T-lymphocyte Jurkat cells that were exposed for 3 h to 0.5 mu M DON. Induction of ER stress by DON was confirmed by immunocytology demonstrating increased protein expression of two major ER stress markers ATF3 and DDIT3. T-cell activation was confirmed by induction of phosphorylation of protein kinases JNK and AKT, activation of NF-kappa B (p65), and increased expression of NFAT target gene NUR77; each of these are known inducers of the T-cell activation response. Induction of an oxidative stress response was also confirmed by monitoring the nuclear translocation of major oxidative stress markers NRF2 and KEAP1, as well as by changes (i.e. decreases) in cell levels of reduced glutathione. Lastly, this study showed that DON induced cleavage of caspase-3, an event known to mediate apoptosis. Taken together, these results allowed us to formulate a potential mechanism of action of DON in immune cells, i.e. binding to eukaryotic 60S ribosomal subunit -> ribotoxic stress -> ER stress -> calcium release from the ER into cytoplasm -> T-cell activation and oxidative stress -> apoptosis. It is proposed that immune cells are more sensitive to DON than other cell types due to the induction of a T-cell activation response by increased intracellular calcium levels.
Databáze: OpenAIRE