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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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 |
format | Article |
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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.</description><identifier>ISSN: 1570-9639</identifier><identifier>ISSN: 0006-3002</identifier><identifier>EISSN: 1878-1454</identifier><identifier>DOI: 10.1016/j.bbapap.2011.04.001</identifier><identifier>PMID: 21513824</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>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</subject><ispartof>Biochimica et biophysica acta, 2011-07, Vol.1814 (7), p.850-857</ispartof><rights>2011 Elsevier B.V.</rights><rights>2011 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-a69811f7a2c37a48b547c2b880a8a789c58e91b205add37bbed2ab9e156081be3</citedby><cites>FETCH-LOGICAL-c464t-a69811f7a2c37a48b547c2b880a8a789c58e91b205add37bbed2ab9e156081be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1570963911000690$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21513824$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nogueira da Costa, André</creatorcontrib><creatorcontrib>Keen, Jeffrey N.</creatorcontrib><creatorcontrib>Wild, Christopher P.</creatorcontrib><creatorcontrib>Findlay, John B.C.</creatorcontrib><title>An analysis of the phosphoproteome of immune cell lines exposed to the immunomodulatory mycotoxin deoxynivalenol</title><title>Biochimica et biophysica acta</title><addtitle>Biochim Biophys Acta</addtitle><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.</description><subject>B-Lymphocytes - drug effects</subject><subject>B-Lymphocytes - metabolism</subject><subject>biochemical pathways</subject><subject>Biomarker</subject><subject>biomarkers</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>cell lines</subject><subject>Cell Survival - drug effects</subject><subject>Cereals</subject><subject>Deoxynivalenol</subject><subject>diet</subject><subject>Diets</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electrophoresis, Gel, Two-Dimensional</subject><subject>Elongation</subject><subject>Flow Cytometry</subject><subject>Gel electrophoresis</subject><subject>gels</subject><subject>Grain</subject><subject>Growth factors</subject><subject>heat</subject><subject>Heat shock</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunomodulation</subject><subject>Immunotoxicity</subject><subject>Lymphocytes</subject><subject>Lymphocytes - drug effects</subject><subject>Lymphocytes - metabolism</subject><subject>Lymphocytes T</subject><subject>Metabolic pathways</subject><subject>Mycotoxin</subject><subject>Mycotoxins</subject><subject>Mycotoxins - pharmacology</subject><subject>Nucleoside-diphosphate kinase</subject><subject>Phosphoproteins</subject><subject>Phosphoproteins - analysis</subject><subject>phosphoproteomes</subject><subject>Phosphoproteomics</subject><subject>Phosphorylation</subject><subject>Phosphorylation - drug effects</subject><subject>Protein biosynthesis</subject><subject>protein synthesis</subject><subject>Proteome - analysis</subject><subject>Proteome - metabolism</subject><subject>proteomics</subject><subject>Proteomics - methods</subject><subject>Reproducibility of Results</subject><subject>Signal transduction</subject><subject>small cereal grains</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>T-Lymphocytes - drug effects</subject><subject>T-Lymphocytes - metabolism</subject><subject>Time Factors</subject><subject>Translation initiation</subject><subject>Trichothecenes - pharmacology</subject><subject>two-dimensional gel electrophoresis</subject><subject>Vomitoxin</subject><issn>1570-9639</issn><issn>0006-3002</issn><issn>1878-1454</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kV9v1iAUh4nRuDn9Bka59KYVWij0xmRZpjNZ4oXumvDn1PGmhQrt8vbby7tOL3dBIOT5nXN4QOg9JTUltPt8qI3Rs57rhlBaE1YTQl-gcyqFrCjj7GU5c0Gqvmv7M_Qm5wMhDRGCv0ZnDeW0lQ07R_NlwDroccs-4zjg5R7wfB9zWXOKC8QJTtd-mtYA2MI44tEHyBiOc8zg8BIfM49AnKJbR73EtOFps3GJRx-wg3jcgn_QI4Q4vkWvBj1mePe0X6C7r9e_rm6q2x_fvl9d3laWdWypdNdLSgehG9sKzaThTNjGSEm01EL2lkvoqWkI1861whhwjTY9UN4RSQ20F-jTXrc8488KeVGTz6f5dYC4ZkUJkcVA38qCsh21KeacYFBz8pNOW4HUybU6qN21OrlWhKniusQ-PHVYzQTuf-if3AJ83IFBR6V_J5_V3c9SgZePoKyVfSG-7AQUEw8eksrWQ7DgfAK7KBf98zP8BUqxnXg</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Nogueira da Costa, André</creator><creator>Keen, Jeffrey N.</creator><creator>Wild, Christopher P.</creator><creator>Findlay, John B.C.</creator><general>Elsevier B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20110701</creationdate><title>An analysis of the phosphoproteome of immune cell lines exposed to the immunomodulatory mycotoxin deoxynivalenol</title><author>Nogueira da Costa, André ; Keen, Jeffrey N. ; Wild, Christopher P. ; Findlay, John B.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-a69811f7a2c37a48b547c2b880a8a789c58e91b205add37bbed2ab9e156081be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>B-Lymphocytes - drug effects</topic><topic>B-Lymphocytes - metabolism</topic><topic>biochemical pathways</topic><topic>Biomarker</topic><topic>biomarkers</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>cell lines</topic><topic>Cell Survival - drug effects</topic><topic>Cereals</topic><topic>Deoxynivalenol</topic><topic>diet</topic><topic>Diets</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electrophoresis, Gel, Two-Dimensional</topic><topic>Elongation</topic><topic>Flow Cytometry</topic><topic>Gel electrophoresis</topic><topic>gels</topic><topic>Grain</topic><topic>Growth factors</topic><topic>heat</topic><topic>Heat shock</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunomodulation</topic><topic>Immunotoxicity</topic><topic>Lymphocytes</topic><topic>Lymphocytes - drug effects</topic><topic>Lymphocytes - metabolism</topic><topic>Lymphocytes T</topic><topic>Metabolic pathways</topic><topic>Mycotoxin</topic><topic>Mycotoxins</topic><topic>Mycotoxins - pharmacology</topic><topic>Nucleoside-diphosphate kinase</topic><topic>Phosphoproteins</topic><topic>Phosphoproteins - analysis</topic><topic>phosphoproteomes</topic><topic>Phosphoproteomics</topic><topic>Phosphorylation</topic><topic>Phosphorylation - drug effects</topic><topic>Protein biosynthesis</topic><topic>protein synthesis</topic><topic>Proteome - analysis</topic><topic>Proteome - metabolism</topic><topic>proteomics</topic><topic>Proteomics - methods</topic><topic>Reproducibility of Results</topic><topic>Signal transduction</topic><topic>small cereal grains</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>T-Lymphocytes - drug effects</topic><topic>T-Lymphocytes - metabolism</topic><topic>Time Factors</topic><topic>Translation initiation</topic><topic>Trichothecenes - pharmacology</topic><topic>two-dimensional gel electrophoresis</topic><topic>Vomitoxin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nogueira da Costa, André</creatorcontrib><creatorcontrib>Keen, Jeffrey N.</creatorcontrib><creatorcontrib>Wild, Christopher P.</creatorcontrib><creatorcontrib>Findlay, John B.C.</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Biochimica et biophysica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nogueira da Costa, André</au><au>Keen, Jeffrey N.</au><au>Wild, Christopher P.</au><au>Findlay, John B.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An analysis of the phosphoproteome of immune cell lines exposed to the immunomodulatory mycotoxin deoxynivalenol</atitle><jtitle>Biochimica et biophysica acta</jtitle><addtitle>Biochim Biophys Acta</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>1814</volume><issue>7</issue><spage>850</spage><epage>857</epage><pages>850-857</pages><issn>1570-9639</issn><issn>0006-3002</issn><eissn>1878-1454</eissn><abstract>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.</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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