Correlation of Taurine Transport with Membrane Lipid Composition and Peroxidation in DHA-Enriched Caco-2 Cells
Diets supplemented with n-3 polyunsaturated fatty acids can promote lipid peroxidation and the propagation of oxygen radicals. These effects can be prevented by taurine, a functional ingredient with antioxidant properties. Here, we examined whether there is a correlation between transepithelial taur...
Gespeichert in:
Veröffentlicht in: | The Journal of membrane biology 2009-04, Vol.228 (3), p.141-150 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 150 |
---|---|
container_issue | 3 |
container_start_page | 141 |
container_title | The Journal of membrane biology |
container_volume | 228 |
creator | Roig-Pérez, Sònia Ferrer, Carmen Rafecas, Magda Moretó, Miquel Ferrer, Ruth |
description | Diets supplemented with n-3 polyunsaturated fatty acids can promote lipid peroxidation and the propagation of oxygen radicals. These effects can be prevented by taurine, a functional ingredient with antioxidant properties. Here, we examined whether there is a correlation between transepithelial taurine transport, on the one hand, and membrane fatty acid composition and peroxidation in intestinal Caco-2 cells, on the other. Differentiated Caco-2 cells were maintained for 10 days, from the day of confluence, in control conditions or in a medium enriched with docosahexaenoic acid (DHA, 100 μmol/l), taurine (10 mmol/l) or DHA plus taurine. Incubation of the monolayers in a medium enriched with DHA increased the incorporation of this fatty acid into the brush-border membrane, at the expense of total n-6 fatty acids (C20:2n-6, C20:3n-6 and C22:4n-6). This was paralleled by increased membrane lipid peroxidation, which was partially limited by the addition of taurine. Transepithelial taurine transport was estimated from taurine uptake and efflux kinetic parameters at apical and basolateral domains. Cell incubation with DHA increased basolateral taurine uptake through an increase in V max, whereas incubation with taurine downregulated basolateral uptake as occurred for apical taurine transporter. Moreover, addition of DHA reduced the apical downregulation effect exerted on taurine transport by taurine incubation. Our results suggest that the oxidative status of epithelial cells regulates taurine transport, thus satisfying antioxidant cellular requirements. |
doi_str_mv | 10.1007/s00232-009-9166-4 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67240431</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67240431</sourcerecordid><originalsourceid>FETCH-LOGICAL-c393t-5e0606ef0a554121981132646dea0f6ed57c6530903ef39881852f622cc32d033</originalsourceid><addsrcrecordid>eNp9kUFv1DAQhS0EotvCD-ACFofeDDMex9kcq1Ao0iKQ2J4tN3FaVxs72ImAf49LVqrEgZOlme89z8xj7BXCOwSo32cASVIANKJBrYV6wjaoSgWVVE_ZprSlkJrwhJ3mfA-Ada3Vc3aCDVVAqDYstDEld7Czj4HHge_tknxwfJ9syFNMM__p5zv-xY03peL4zk--520cp5j9X5ENPf_mUvzl-9XFB_7h6kJchuS7O1dg20UheesOh_yCPRvsIbuXx_eMXX-83LdXYvf10-f2Yic6amgWlQMN2g1gq0qhxGaLSFIr3TsLg3Z9VXe6ImiA3EDNdovbSg5ayq4j2QPRGTtffacUfywuz2b0uSsTlB3iko2upQJFWMC3_4D3cUmhzGYk1qoq19QFwhXqUsw5ucFMyY82_TYI5iEJsyZhShLmIQmjiub10Xi5GV3_qDievgByBXJphVuXHn_-n-ubVTTYaOxt8tlcf5eABFhipkbSH-oGmnw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>217454326</pqid></control><display><type>article</type><title>Correlation of Taurine Transport with Membrane Lipid Composition and Peroxidation in DHA-Enriched Caco-2 Cells</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Roig-Pérez, Sònia ; Ferrer, Carmen ; Rafecas, Magda ; Moretó, Miquel ; Ferrer, Ruth</creator><creatorcontrib>Roig-Pérez, Sònia ; Ferrer, Carmen ; Rafecas, Magda ; Moretó, Miquel ; Ferrer, Ruth</creatorcontrib><description>Diets supplemented with n-3 polyunsaturated fatty acids can promote lipid peroxidation and the propagation of oxygen radicals. These effects can be prevented by taurine, a functional ingredient with antioxidant properties. Here, we examined whether there is a correlation between transepithelial taurine transport, on the one hand, and membrane fatty acid composition and peroxidation in intestinal Caco-2 cells, on the other. Differentiated Caco-2 cells were maintained for 10 days, from the day of confluence, in control conditions or in a medium enriched with docosahexaenoic acid (DHA, 100 μmol/l), taurine (10 mmol/l) or DHA plus taurine. Incubation of the monolayers in a medium enriched with DHA increased the incorporation of this fatty acid into the brush-border membrane, at the expense of total n-6 fatty acids (C20:2n-6, C20:3n-6 and C22:4n-6). This was paralleled by increased membrane lipid peroxidation, which was partially limited by the addition of taurine. Transepithelial taurine transport was estimated from taurine uptake and efflux kinetic parameters at apical and basolateral domains. Cell incubation with DHA increased basolateral taurine uptake through an increase in V max, whereas incubation with taurine downregulated basolateral uptake as occurred for apical taurine transporter. Moreover, addition of DHA reduced the apical downregulation effect exerted on taurine transport by taurine incubation. Our results suggest that the oxidative status of epithelial cells regulates taurine transport, thus satisfying antioxidant cellular requirements.</description><identifier>ISSN: 0022-2631</identifier><identifier>EISSN: 1432-1424</identifier><identifier>DOI: 10.1007/s00232-009-9166-4</identifier><identifier>PMID: 19350314</identifier><language>eng</language><publisher>New York: New York : Springer-Verlag</publisher><subject>Biochemistry ; Biomedical and Life Sciences ; Caco-2 Cells ; Cell Membrane - drug effects ; Cell Membrane - metabolism ; Cellular biology ; Docosahexaenoic Acids - metabolism ; Fatty acids ; Human Physiology ; Humans ; Life Sciences ; Lipid Peroxidation - drug effects ; Membrane Lipids - chemistry ; Membranes ; Oxidation ; Taurine - metabolism</subject><ispartof>The Journal of membrane biology, 2009-04, Vol.228 (3), p.141-150</ispartof><rights>Springer Science+Business Media, LLC 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-5e0606ef0a554121981132646dea0f6ed57c6530903ef39881852f622cc32d033</citedby><cites>FETCH-LOGICAL-c393t-5e0606ef0a554121981132646dea0f6ed57c6530903ef39881852f622cc32d033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00232-009-9166-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00232-009-9166-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19350314$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roig-Pérez, Sònia</creatorcontrib><creatorcontrib>Ferrer, Carmen</creatorcontrib><creatorcontrib>Rafecas, Magda</creatorcontrib><creatorcontrib>Moretó, Miquel</creatorcontrib><creatorcontrib>Ferrer, Ruth</creatorcontrib><title>Correlation of Taurine Transport with Membrane Lipid Composition and Peroxidation in DHA-Enriched Caco-2 Cells</title><title>The Journal of membrane biology</title><addtitle>J Membrane Biol</addtitle><addtitle>J Membr Biol</addtitle><description>Diets supplemented with n-3 polyunsaturated fatty acids can promote lipid peroxidation and the propagation of oxygen radicals. These effects can be prevented by taurine, a functional ingredient with antioxidant properties. Here, we examined whether there is a correlation between transepithelial taurine transport, on the one hand, and membrane fatty acid composition and peroxidation in intestinal Caco-2 cells, on the other. Differentiated Caco-2 cells were maintained for 10 days, from the day of confluence, in control conditions or in a medium enriched with docosahexaenoic acid (DHA, 100 μmol/l), taurine (10 mmol/l) or DHA plus taurine. Incubation of the monolayers in a medium enriched with DHA increased the incorporation of this fatty acid into the brush-border membrane, at the expense of total n-6 fatty acids (C20:2n-6, C20:3n-6 and C22:4n-6). This was paralleled by increased membrane lipid peroxidation, which was partially limited by the addition of taurine. Transepithelial taurine transport was estimated from taurine uptake and efflux kinetic parameters at apical and basolateral domains. Cell incubation with DHA increased basolateral taurine uptake through an increase in V max, whereas incubation with taurine downregulated basolateral uptake as occurred for apical taurine transporter. Moreover, addition of DHA reduced the apical downregulation effect exerted on taurine transport by taurine incubation. Our results suggest that the oxidative status of epithelial cells regulates taurine transport, thus satisfying antioxidant cellular requirements.</description><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Caco-2 Cells</subject><subject>Cell Membrane - drug effects</subject><subject>Cell Membrane - metabolism</subject><subject>Cellular biology</subject><subject>Docosahexaenoic Acids - metabolism</subject><subject>Fatty acids</subject><subject>Human Physiology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Membrane Lipids - chemistry</subject><subject>Membranes</subject><subject>Oxidation</subject><subject>Taurine - metabolism</subject><issn>0022-2631</issn><issn>1432-1424</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kUFv1DAQhS0EotvCD-ACFofeDDMex9kcq1Ao0iKQ2J4tN3FaVxs72ImAf49LVqrEgZOlme89z8xj7BXCOwSo32cASVIANKJBrYV6wjaoSgWVVE_ZprSlkJrwhJ3mfA-Ada3Vc3aCDVVAqDYstDEld7Czj4HHge_tknxwfJ9syFNMM__p5zv-xY03peL4zk--520cp5j9X5ENPf_mUvzl-9XFB_7h6kJchuS7O1dg20UheesOh_yCPRvsIbuXx_eMXX-83LdXYvf10-f2Yic6amgWlQMN2g1gq0qhxGaLSFIr3TsLg3Z9VXe6ImiA3EDNdovbSg5ayq4j2QPRGTtffacUfywuz2b0uSsTlB3iko2upQJFWMC3_4D3cUmhzGYk1qoq19QFwhXqUsw5ucFMyY82_TYI5iEJsyZhShLmIQmjiub10Xi5GV3_qDievgByBXJphVuXHn_-n-ubVTTYaOxt8tlcf5eABFhipkbSH-oGmnw</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Roig-Pérez, Sònia</creator><creator>Ferrer, Carmen</creator><creator>Rafecas, Magda</creator><creator>Moretó, Miquel</creator><creator>Ferrer, Ruth</creator><general>New York : Springer-Verlag</general><general>Springer-Verlag</general><general>Springer Nature 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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20090401</creationdate><title>Correlation of Taurine Transport with Membrane Lipid Composition and Peroxidation in DHA-Enriched Caco-2 Cells</title><author>Roig-Pérez, Sònia ; Ferrer, Carmen ; Rafecas, Magda ; Moretó, Miquel ; Ferrer, Ruth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-5e0606ef0a554121981132646dea0f6ed57c6530903ef39881852f622cc32d033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Caco-2 Cells</topic><topic>Cell Membrane - drug effects</topic><topic>Cell Membrane - metabolism</topic><topic>Cellular biology</topic><topic>Docosahexaenoic Acids - metabolism</topic><topic>Fatty acids</topic><topic>Human Physiology</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Membrane Lipids - chemistry</topic><topic>Membranes</topic><topic>Oxidation</topic><topic>Taurine - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roig-Pérez, Sònia</creatorcontrib><creatorcontrib>Ferrer, Carmen</creatorcontrib><creatorcontrib>Rafecas, Magda</creatorcontrib><creatorcontrib>Moretó, Miquel</creatorcontrib><creatorcontrib>Ferrer, Ruth</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>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of membrane biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roig-Pérez, Sònia</au><au>Ferrer, Carmen</au><au>Rafecas, Magda</au><au>Moretó, Miquel</au><au>Ferrer, Ruth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation of Taurine Transport with Membrane Lipid Composition and Peroxidation in DHA-Enriched Caco-2 Cells</atitle><jtitle>The Journal of membrane biology</jtitle><stitle>J Membrane Biol</stitle><addtitle>J Membr Biol</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>228</volume><issue>3</issue><spage>141</spage><epage>150</epage><pages>141-150</pages><issn>0022-2631</issn><eissn>1432-1424</eissn><abstract>Diets supplemented with n-3 polyunsaturated fatty acids can promote lipid peroxidation and the propagation of oxygen radicals. These effects can be prevented by taurine, a functional ingredient with antioxidant properties. Here, we examined whether there is a correlation between transepithelial taurine transport, on the one hand, and membrane fatty acid composition and peroxidation in intestinal Caco-2 cells, on the other. Differentiated Caco-2 cells were maintained for 10 days, from the day of confluence, in control conditions or in a medium enriched with docosahexaenoic acid (DHA, 100 μmol/l), taurine (10 mmol/l) or DHA plus taurine. Incubation of the monolayers in a medium enriched with DHA increased the incorporation of this fatty acid into the brush-border membrane, at the expense of total n-6 fatty acids (C20:2n-6, C20:3n-6 and C22:4n-6). This was paralleled by increased membrane lipid peroxidation, which was partially limited by the addition of taurine. Transepithelial taurine transport was estimated from taurine uptake and efflux kinetic parameters at apical and basolateral domains. Cell incubation with DHA increased basolateral taurine uptake through an increase in V max, whereas incubation with taurine downregulated basolateral uptake as occurred for apical taurine transporter. Moreover, addition of DHA reduced the apical downregulation effect exerted on taurine transport by taurine incubation. Our results suggest that the oxidative status of epithelial cells regulates taurine transport, thus satisfying antioxidant cellular requirements.</abstract><cop>New York</cop><pub>New York : Springer-Verlag</pub><pmid>19350314</pmid><doi>10.1007/s00232-009-9166-4</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-2631 |
ispartof | The Journal of membrane biology, 2009-04, Vol.228 (3), p.141-150 |
issn | 0022-2631 1432-1424 |
language | eng |
recordid | cdi_proquest_miscellaneous_67240431 |
source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Biochemistry Biomedical and Life Sciences Caco-2 Cells Cell Membrane - drug effects Cell Membrane - metabolism Cellular biology Docosahexaenoic Acids - metabolism Fatty acids Human Physiology Humans Life Sciences Lipid Peroxidation - drug effects Membrane Lipids - chemistry Membranes Oxidation Taurine - metabolism |
title | Correlation of Taurine Transport with Membrane Lipid Composition and Peroxidation in DHA-Enriched Caco-2 Cells |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T12%3A33%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Correlation%20of%20Taurine%20Transport%20with%20Membrane%20Lipid%20Composition%20and%20Peroxidation%20in%20DHA-Enriched%20Caco-2%20Cells&rft.jtitle=The%20Journal%20of%20membrane%20biology&rft.au=Roig-P%C3%A9rez,%20S%C3%B2nia&rft.date=2009-04-01&rft.volume=228&rft.issue=3&rft.spage=141&rft.epage=150&rft.pages=141-150&rft.issn=0022-2631&rft.eissn=1432-1424&rft_id=info:doi/10.1007/s00232-009-9166-4&rft_dat=%3Cproquest_cross%3E67240431%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=217454326&rft_id=info:pmid/19350314&rfr_iscdi=true |