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Exploring the interactions between polyunsaturated fatty acids and cadmium in rainbow trout liver cells: a genetic and proteomic study.

Identifieur interne : 000268 ( Main/Exploration ); précédent : 000267; suivant : 000269

Exploring the interactions between polyunsaturated fatty acids and cadmium in rainbow trout liver cells: a genetic and proteomic study.

Auteurs : Aline Ferain [Belgique] ; Chloé Bonnineau [France] ; Ineke Neefs [Belgique] ; Nancy De Saeyer [Belgique] ; Benjamin Lemaire [Belgique] ; Valérie Cornet [Belgique] ; Yvan Larondelle [Belgique] ; Karel A C. De Schamphelaere [Belgique] ; Cathy Debier [Belgique] ; Jean-François Rees [Belgique]

Source :

RBID : pubmed:30352337

Descripteurs français

English descriptors

Abstract

Polyunsaturated fatty acids (PUFAs) have key biological roles in fish cells. We recently showed that the phospholipid composition of rainbow trout liver cells (RTL-W1 cell line) modulates their tolerance to an acute cadmium (Cd) challenge. Here, we investigated (i) the extent to which PUFAs and Cd impact fatty acid homeostasis and metabolism in these cells and (ii) possible mechanisms by which specific PUFAs may confer cytoprotection against Cd. First, RTL-W1 cells were cultivated for one week in growth media spiked with 50 μmol L-1 of either alpha-linolenic acid (ALA, 18:3n-3), eicosapentaenoic acid (EPA, 20:5n-3), linoleic acid (LA, 18:2n-6) or arachidonic acid (AA, 20:4n-6) in order to modulate their fatty acid profile. Then, the cells were challenged with Cd (0, 50 or 100 μmol L-1) for 24 h prior to assaying viability, fatty acid profile, intracellular Cd content, proteomic landscape and expression levels of genes involved in fatty acid metabolism, synthesis of PUFA-derived signalling molecules and stress response. We observed that the fatty acid supply and, to a lesser extent, the exposure to Cd influenced cellular fatty acid homeostasis and metabolism. The cellular fatty acid composition of fish liver cells modulated their tolerance to an acute Cd challenge. Enrichments in ALA, EPA, and, to a lesser extent, AA conferred cytoprotection while enrichment in LA had no impact on cell viability. The present study ruled out the possibility that cytoprotection reflects a decreased Cd burden. Our results rather suggest that the PUFA-derived cytoprotection against Cd occurs through a reduction of the oxidative stress induced by Cd and a differential induction of the eicosanoid cascade, with a possible role of peroxiredoxin and glutaredoxin (antioxidant enzymes) as well as cytosolic phospholipase A2 (enzyme initiating the eicosanoid cascade).

DOI: 10.1016/j.aquatox.2018.09.005
PubMed: 30352337


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<term>Animals (MeSH)</term>
<term>Cadmium (metabolism)</term>
<term>Fatty Acids, Unsaturated (metabolism)</term>
<term>Hepatocytes (metabolism)</term>
<term>Lipid Metabolism (genetics)</term>
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<term>Cadmium (métabolisme)</term>
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<term>Métabolisme lipidique (génétique)</term>
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<term>Oncorhynchus mykiss</term>
<term>Phospholipides</term>
<term>Polluants chimiques de l'eau</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Proteomics</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Protéomique</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Polyunsaturated fatty acids (PUFAs) have key biological roles in fish cells. We recently showed that the phospholipid composition of rainbow trout liver cells (RTL-W1 cell line) modulates their tolerance to an acute cadmium (Cd) challenge. Here, we investigated (i) the extent to which PUFAs and Cd impact fatty acid homeostasis and metabolism in these cells and (ii) possible mechanisms by which specific PUFAs may confer cytoprotection against Cd. First, RTL-W1 cells were cultivated for one week in growth media spiked with 50 μmol L
<sup>-1</sup>
of either alpha-linolenic acid (ALA, 18:3n-3), eicosapentaenoic acid (EPA, 20:5n-3), linoleic acid (LA, 18:2n-6) or arachidonic acid (AA, 20:4n-6) in order to modulate their fatty acid profile. Then, the cells were challenged with Cd (0, 50 or 100 μmol L
<sup>-1</sup>
) for 24 h prior to assaying viability, fatty acid profile, intracellular Cd content, proteomic landscape and expression levels of genes involved in fatty acid metabolism, synthesis of PUFA-derived signalling molecules and stress response. We observed that the fatty acid supply and, to a lesser extent, the exposure to Cd influenced cellular fatty acid homeostasis and metabolism. The cellular fatty acid composition of fish liver cells modulated their tolerance to an acute Cd challenge. Enrichments in ALA, EPA, and, to a lesser extent, AA conferred cytoprotection while enrichment in LA had no impact on cell viability. The present study ruled out the possibility that cytoprotection reflects a decreased Cd burden. Our results rather suggest that the PUFA-derived cytoprotection against Cd occurs through a reduction of the oxidative stress induced by Cd and a differential induction of the eicosanoid cascade, with a possible role of peroxiredoxin and glutaredoxin (antioxidant enzymes) as well as cytosolic phospholipase A2 (enzyme initiating the eicosanoid cascade).</div>
</front>
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<DateCompleted>
<Year>2018</Year>
<Month>12</Month>
<Day>12</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>12</Month>
<Day>12</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1879-1514</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>205</Volume>
<PubDate>
<Year>2018</Year>
<Month>Dec</Month>
</PubDate>
</JournalIssue>
<Title>Aquatic toxicology (Amsterdam, Netherlands)</Title>
<ISOAbbreviation>Aquat Toxicol</ISOAbbreviation>
</Journal>
<ArticleTitle>Exploring the interactions between polyunsaturated fatty acids and cadmium in rainbow trout liver cells: a genetic and proteomic study.</ArticleTitle>
<Pagination>
<MedlinePgn>100-113</MedlinePgn>
</Pagination>
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<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.aquatox.2018.09.005</ELocationID>
<Abstract>
<AbstractText>Polyunsaturated fatty acids (PUFAs) have key biological roles in fish cells. We recently showed that the phospholipid composition of rainbow trout liver cells (RTL-W1 cell line) modulates their tolerance to an acute cadmium (Cd) challenge. Here, we investigated (i) the extent to which PUFAs and Cd impact fatty acid homeostasis and metabolism in these cells and (ii) possible mechanisms by which specific PUFAs may confer cytoprotection against Cd. First, RTL-W1 cells were cultivated for one week in growth media spiked with 50 μmol L
<sup>-1</sup>
of either alpha-linolenic acid (ALA, 18:3n-3), eicosapentaenoic acid (EPA, 20:5n-3), linoleic acid (LA, 18:2n-6) or arachidonic acid (AA, 20:4n-6) in order to modulate their fatty acid profile. Then, the cells were challenged with Cd (0, 50 or 100 μmol L
<sup>-1</sup>
) for 24 h prior to assaying viability, fatty acid profile, intracellular Cd content, proteomic landscape and expression levels of genes involved in fatty acid metabolism, synthesis of PUFA-derived signalling molecules and stress response. We observed that the fatty acid supply and, to a lesser extent, the exposure to Cd influenced cellular fatty acid homeostasis and metabolism. The cellular fatty acid composition of fish liver cells modulated their tolerance to an acute Cd challenge. Enrichments in ALA, EPA, and, to a lesser extent, AA conferred cytoprotection while enrichment in LA had no impact on cell viability. The present study ruled out the possibility that cytoprotection reflects a decreased Cd burden. Our results rather suggest that the PUFA-derived cytoprotection against Cd occurs through a reduction of the oxidative stress induced by Cd and a differential induction of the eicosanoid cascade, with a possible role of peroxiredoxin and glutaredoxin (antioxidant enzymes) as well as cytosolic phospholipase A2 (enzyme initiating the eicosanoid cascade).</AbstractText>
<CopyrightInformation>Copyright © 2018 Elsevier B.V. All rights reserved.</CopyrightInformation>
</Abstract>
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<Author ValidYN="Y">
<LastName>Ferain</LastName>
<ForeName>Aline</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Louvain Institute of Biomolecular Science and Technology, Université catholique de Louvain, Croix du Sud 2/L7.05.08, B-1348 Louvain-la-Neuve, Belgium. Electronic address: aline.ferain@uclouvain.be.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bonnineau</LastName>
<ForeName>Chloé</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Irstea, UR RiverLy, Centre de Lyon-Villeurbanne, 5, 69625 Villeurbanne, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Neefs</LastName>
<ForeName>Ineke</ForeName>
<Initials>I</Initials>
<AffiliationInfo>
<Affiliation>Louvain Institute of Biomolecular Science and Technology, Université catholique de Louvain, Croix du Sud 2/L7.05.08, B-1348 Louvain-la-Neuve, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>De Saeyer</LastName>
<ForeName>Nancy</ForeName>
<Initials>N</Initials>
<AffiliationInfo>
<Affiliation>Laboratory of Environmental Toxicology and Aquatic Ecology, Environmental Toxicology Unit, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lemaire</LastName>
<ForeName>Benjamin</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>Louvain Institute of Biomolecular Science and Technology, Université catholique de Louvain, Croix du Sud 2/L7.05.08, B-1348 Louvain-la-Neuve, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Cornet</LastName>
<ForeName>Valérie</ForeName>
<Initials>V</Initials>
<AffiliationInfo>
<Affiliation>Research Unit in Environmental and Evolutionary Biology (URBE), University of Namur, B-5000 Namur, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Larondelle</LastName>
<ForeName>Yvan</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>Louvain Institute of Biomolecular Science and Technology, Université catholique de Louvain, Croix du Sud 2/L7.05.08, B-1348 Louvain-la-Neuve, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>De Schamphelaere</LastName>
<ForeName>Karel A C</ForeName>
<Initials>KAC</Initials>
<AffiliationInfo>
<Affiliation>Laboratory of Environmental Toxicology and Aquatic Ecology, Environmental Toxicology Unit, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Debier</LastName>
<ForeName>Cathy</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Louvain Institute of Biomolecular Science and Technology, Université catholique de Louvain, Croix du Sud 2/L7.05.08, B-1348 Louvain-la-Neuve, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Rees</LastName>
<ForeName>Jean-François</ForeName>
<Initials>JF</Initials>
<AffiliationInfo>
<Affiliation>Louvain Institute of Biomolecular Science and Technology, Université catholique de Louvain, Croix du Sud 2/L7.05.08, B-1348 Louvain-la-Neuve, Belgium. Electronic address: jf.rees@uclouvain.be.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2018</Year>
<Month>09</Month>
<Day>22</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>Netherlands</Country>
<MedlineTA>Aquat Toxicol</MedlineTA>
<NlmUniqueID>8500246</NlmUniqueID>
<ISSNLinking>0166-445X</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D005231">Fatty Acids, Unsaturated</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D010743">Phospholipids</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D014874">Water Pollutants, Chemical</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>00BH33GNGH</RegistryNumber>
<NameOfSubstance UI="D002104">Cadmium</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D002104" MajorTopicYN="N">Cadmium</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005231" MajorTopicYN="N">Fatty Acids, Unsaturated</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D022781" MajorTopicYN="N">Hepatocytes</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D050356" MajorTopicYN="N">Lipid Metabolism</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D017686" MajorTopicYN="N">Oncorhynchus mykiss</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018384" MajorTopicYN="N">Oxidative Stress</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010743" MajorTopicYN="N">Phospholipids</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D040901" MajorTopicYN="N">Proteomics</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D014874" MajorTopicYN="N">Water Pollutants, Chemical</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Cadmium</Keyword>
<Keyword MajorTopicYN="N">Gene expression</Keyword>
<Keyword MajorTopicYN="N">Polyunsaturated fatty acids</Keyword>
<Keyword MajorTopicYN="N">Proteomics</Keyword>
<Keyword MajorTopicYN="N">RTL-W1 cells</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2018</Year>
<Month>07</Month>
<Day>30</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised">
<Year>2018</Year>
<Month>09</Month>
<Day>07</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2018</Year>
<Month>09</Month>
<Day>10</Day>
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<Year>2018</Year>
<Month>10</Month>
<Day>24</Day>
<Hour>6</Hour>
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<PubMedPubDate PubStatus="medline">
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<PubMedPubDate PubStatus="entrez">
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</ArticleIdList>
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<list>
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<li>Belgique</li>
<li>France</li>
</country>
<region>
<li>Auvergne-Rhône-Alpes</li>
<li>Province de Flandre-Orientale</li>
<li>Province du Brabant wallon</li>
<li>Rhône-Alpes</li>
<li>Région flamande</li>
<li>Région wallonne</li>
</region>
<settlement>
<li>Gand</li>
<li>Louvain-la-Neuve</li>
<li>Villeurbanne</li>
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<li>Université catholique de Louvain</li>
<li>Université de Gand</li>
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<region name="Région wallonne">
<name sortKey="Ferain, Aline" sort="Ferain, Aline" uniqKey="Ferain A" first="Aline" last="Ferain">Aline Ferain</name>
</region>
<name sortKey="Cornet, Valerie" sort="Cornet, Valerie" uniqKey="Cornet V" first="Valérie" last="Cornet">Valérie Cornet</name>
<name sortKey="De Saeyer, Nancy" sort="De Saeyer, Nancy" uniqKey="De Saeyer N" first="Nancy" last="De Saeyer">Nancy De Saeyer</name>
<name sortKey="De Schamphelaere, Karel A C" sort="De Schamphelaere, Karel A C" uniqKey="De Schamphelaere K" first="Karel A C" last="De Schamphelaere">Karel A C. De Schamphelaere</name>
<name sortKey="Debier, Cathy" sort="Debier, Cathy" uniqKey="Debier C" first="Cathy" last="Debier">Cathy Debier</name>
<name sortKey="Larondelle, Yvan" sort="Larondelle, Yvan" uniqKey="Larondelle Y" first="Yvan" last="Larondelle">Yvan Larondelle</name>
<name sortKey="Lemaire, Benjamin" sort="Lemaire, Benjamin" uniqKey="Lemaire B" first="Benjamin" last="Lemaire">Benjamin Lemaire</name>
<name sortKey="Neefs, Ineke" sort="Neefs, Ineke" uniqKey="Neefs I" first="Ineke" last="Neefs">Ineke Neefs</name>
<name sortKey="Rees, Jean Francois" sort="Rees, Jean Francois" uniqKey="Rees J" first="Jean-François" last="Rees">Jean-François Rees</name>
</country>
<country name="France">
<region name="Auvergne-Rhône-Alpes">
<name sortKey="Bonnineau, Chloe" sort="Bonnineau, Chloe" uniqKey="Bonnineau C" first="Chloé" last="Bonnineau">Chloé Bonnineau</name>
</region>
</country>
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