An analysis of the phosphoproteome of immune cell lines exposed to the immunomodulatory mycotoxin deoxynivalenol

The mycotoxin deoxynivalenol (DON) commonly contaminates cereal grains. It is ubiquitous in the Western European diet, although chronic, low-dose effects in humans are not well described, but immunotoxicity has been reported. In this study, two-dimensional gel electrophoresis was used to identify ph...

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Veröffentlicht in:Biochimica et biophysica acta 2011-07, Vol.1814 (7), p.850-857
Hauptverfasser: Nogueira da Costa, André, Keen, Jeffrey N., Wild, Christopher P., Findlay, John B.C.
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container_issue 7
container_start_page 850
container_title Biochimica et biophysica acta
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creator Nogueira da Costa, André
Keen, Jeffrey N.
Wild, Christopher P.
Findlay, John B.C.
description The mycotoxin deoxynivalenol (DON) commonly contaminates cereal grains. It is ubiquitous in the Western European diet, although chronic, low-dose effects in humans are not well described, but immunotoxicity has been reported. In this study, two-dimensional gel electrophoresis was used to identify phosphoproteomic changes in human B (RPMI1788) and T (Jurkat E6.1) lymphocyte cell lines after exposure to modest concentrations of DON (up to 500 ng/mL) for 24 h. Proteins identified as having altered phosphorylation state post-treatment (C-1-tetrahydrofolate synthase, eukaryotic elongation factor 2, nucleoside diphosphate kinase A, heat shock cognate 71 kDa protein, eukaryotic translation initiation factor 3 subunit I and growth factor receptor-bound protein 2) are involved in regulation of metabolic pathways, protein biosynthesis and signaling transduction. All exhibited a greater than 1.4-fold change, reproducible in three separate experiments consisting of 36 gels in total. Flow cytometry validated the observations for eukaryotic elongation factor 2 and growth factor receptor-bound protein 2. These findings provide further insights as to how low dose exposure to DON may affect human immune function and may have potential as mechanism-based phosphoprotein biomarkers for DON exposure. ► Deoxynivalenol contaminates cereal grains worldwide. ► Low-dose exposure induces immunotoxicity. ► Deoxynivalenol treatment alters immune cell lines phosphoproteome. ► We identified potential mechanism-based phosphoprotein biomarkers.
doi_str_mv 10.1016/j.bbapap.2011.04.001
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It is ubiquitous in the Western European diet, although chronic, low-dose effects in humans are not well described, but immunotoxicity has been reported. In this study, two-dimensional gel electrophoresis was used to identify phosphoproteomic changes in human B (RPMI1788) and T (Jurkat E6.1) lymphocyte cell lines after exposure to modest concentrations of DON (up to 500 ng/mL) for 24 h. Proteins identified as having altered phosphorylation state post-treatment (C-1-tetrahydrofolate synthase, eukaryotic elongation factor 2, nucleoside diphosphate kinase A, heat shock cognate 71 kDa protein, eukaryotic translation initiation factor 3 subunit I and growth factor receptor-bound protein 2) are involved in regulation of metabolic pathways, protein biosynthesis and signaling transduction. All exhibited a greater than 1.4-fold change, reproducible in three separate experiments consisting of 36 gels in total. Flow cytometry validated the observations for eukaryotic elongation factor 2 and growth factor receptor-bound protein 2. 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It is ubiquitous in the Western European diet, although chronic, low-dose effects in humans are not well described, but immunotoxicity has been reported. In this study, two-dimensional gel electrophoresis was used to identify phosphoproteomic changes in human B (RPMI1788) and T (Jurkat E6.1) lymphocyte cell lines after exposure to modest concentrations of DON (up to 500 ng/mL) for 24 h. Proteins identified as having altered phosphorylation state post-treatment (C-1-tetrahydrofolate synthase, eukaryotic elongation factor 2, nucleoside diphosphate kinase A, heat shock cognate 71 kDa protein, eukaryotic translation initiation factor 3 subunit I and growth factor receptor-bound protein 2) are involved in regulation of metabolic pathways, protein biosynthesis and signaling transduction. All exhibited a greater than 1.4-fold change, reproducible in three separate experiments consisting of 36 gels in total. Flow cytometry validated the observations for eukaryotic elongation factor 2 and growth factor receptor-bound protein 2. 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It is ubiquitous in the Western European diet, although chronic, low-dose effects in humans are not well described, but immunotoxicity has been reported. In this study, two-dimensional gel electrophoresis was used to identify phosphoproteomic changes in human B (RPMI1788) and T (Jurkat E6.1) lymphocyte cell lines after exposure to modest concentrations of DON (up to 500 ng/mL) for 24 h. Proteins identified as having altered phosphorylation state post-treatment (C-1-tetrahydrofolate synthase, eukaryotic elongation factor 2, nucleoside diphosphate kinase A, heat shock cognate 71 kDa protein, eukaryotic translation initiation factor 3 subunit I and growth factor receptor-bound protein 2) are involved in regulation of metabolic pathways, protein biosynthesis and signaling transduction. All exhibited a greater than 1.4-fold change, reproducible in three separate experiments consisting of 36 gels in total. Flow cytometry validated the observations for eukaryotic elongation factor 2 and growth factor receptor-bound protein 2. These findings provide further insights as to how low dose exposure to DON may affect human immune function and may have potential as mechanism-based phosphoprotein biomarkers for DON exposure. ► Deoxynivalenol contaminates cereal grains worldwide. ► Low-dose exposure induces immunotoxicity. ► Deoxynivalenol treatment alters immune cell lines phosphoproteome. ► We identified potential mechanism-based phosphoprotein biomarkers.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>21513824</pmid><doi>10.1016/j.bbapap.2011.04.001</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects B-Lymphocytes - drug effects
B-Lymphocytes - metabolism
biochemical pathways
Biomarker
biomarkers
Cell Line
Cell Line, Tumor
cell lines
Cell Survival - drug effects
Cereals
Deoxynivalenol
diet
Diets
Dose-Response Relationship, Drug
Electrophoresis, Gel, Two-Dimensional
Elongation
Flow Cytometry
Gel electrophoresis
gels
Grain
Growth factors
heat
Heat shock
Humans
Immune response
Immunomodulation
Immunotoxicity
Lymphocytes
Lymphocytes - drug effects
Lymphocytes - metabolism
Lymphocytes T
Metabolic pathways
Mycotoxin
Mycotoxins
Mycotoxins - pharmacology
Nucleoside-diphosphate kinase
Phosphoproteins
Phosphoproteins - analysis
phosphoproteomes
Phosphoproteomics
Phosphorylation
Phosphorylation - drug effects
Protein biosynthesis
protein synthesis
Proteome - analysis
Proteome - metabolism
proteomics
Proteomics - methods
Reproducibility of Results
Signal transduction
small cereal grains
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
T-Lymphocytes - drug effects
T-Lymphocytes - metabolism
Time Factors
Translation initiation
Trichothecenes - pharmacology
two-dimensional gel electrophoresis
Vomitoxin
title An analysis of the phosphoproteome of immune cell lines exposed to the immunomodulatory mycotoxin deoxynivalenol
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