endogenous retinoid metabolite S-4-oxo-9-cis-13,14-dihydro-retinoic acid activates retinoic acid receptor signalling both in vitro and in vivo
Retinoic acid receptor (RAR) and retinoid X receptor are ligand-induced transcription factors that belong to the nuclear receptor family. The receptors are activated by small hydrophobic compounds, such as all-trans-retinoic acid and 9-cis-retinoic acid, respectively. Interestingly, these receptors...
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creator | Schuchardt, Jan P Wahlström, David Rüegg, Joëlle Giese, Norbert Stefan, Madalina Hopf, Henning Pongratz, Ingemar Håkansson, Helen Eichele, Gregor Pettersson, Katarina Nau, Heinz |
description | Retinoic acid receptor (RAR) and retinoid X receptor are ligand-induced transcription factors that belong to the nuclear receptor family. The receptors are activated by small hydrophobic compounds, such as all-trans-retinoic acid and 9-cis-retinoic acid, respectively. Interestingly, these receptors are also targets for a number of exogenous compounds. In this study, we characterized the biological activity of the 9-cis-substituted retinoic acid metabolite, S-4-oxo-9-cis-13,14-dihydro-retinoic acid (S-4o9cDH-RA). The endogenous levels of this metabolite in wild-type mice and rats were found to be higher than those of all-trans-retinoic acid, especially in the liver. Using cell-based luciferase reporter systems, we showed that S-4o9cDH-RA activates the transcription of retinoic acid response element-containing genes in several cell types, both from a simple 2xDR5 element and from the promoter of the natural retinoid target gene RARβ2. In addition, quantitative RT-PCR analysis demonstrated that S-4o9cDH-RA treatment significantly increases the endogenous mRNA levels of the RAR target gene RARβ2. Utilizing a limited proteolytic digestion assay, we showed that S-4o9cDH-RA induces conformational changes to both RARα and RARβ in the same manner as does all-trans-retinoic acid, suggesting that S-4o9cDH-RA is indeed an endogenous ligand for these receptors. These in vitro results were corroborated in an in vivo system, where S-4o9cDH-RA induced morphological changes similar to those of all-trans-retinoic acid in the developing chicken wing bud. When locally applied to the wing bud, S-4o9cDH-RA induced digit pattern duplications in a dose-dependent fashion. The results illustrate that S-4o9cDH-RA closely mimics all-trans-retinoic acid with regard to pattern respecification. Finally, using quantitative RT-PCR analysis, we showed that S-4o9cDH-RA induces the transcription of several retinoic acid-regulated genes in chick wing buds, including Hoxb8, RARβ2, shh, Cyp26 and bmp2. Although S-4o9cDH-RA was less potent when compared with all-trans-retinoic acid, the findings clearly demonstrate that S-4o9cDH-RA has the capacity to bind and activate nuclear retinoid receptors and regulate gene transcription both in vitro and in vivo. |
doi_str_mv | 10.1111/j.1742-4658.2009.07023.x |
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The receptors are activated by small hydrophobic compounds, such as all-trans-retinoic acid and 9-cis-retinoic acid, respectively. Interestingly, these receptors are also targets for a number of exogenous compounds. In this study, we characterized the biological activity of the 9-cis-substituted retinoic acid metabolite, S-4-oxo-9-cis-13,14-dihydro-retinoic acid (S-4o9cDH-RA). The endogenous levels of this metabolite in wild-type mice and rats were found to be higher than those of all-trans-retinoic acid, especially in the liver. Using cell-based luciferase reporter systems, we showed that S-4o9cDH-RA activates the transcription of retinoic acid response element-containing genes in several cell types, both from a simple 2xDR5 element and from the promoter of the natural retinoid target gene RARβ2. In addition, quantitative RT-PCR analysis demonstrated that S-4o9cDH-RA treatment significantly increases the endogenous mRNA levels of the RAR target gene RARβ2. Utilizing a limited proteolytic digestion assay, we showed that S-4o9cDH-RA induces conformational changes to both RARα and RARβ in the same manner as does all-trans-retinoic acid, suggesting that S-4o9cDH-RA is indeed an endogenous ligand for these receptors. These in vitro results were corroborated in an in vivo system, where S-4o9cDH-RA induced morphological changes similar to those of all-trans-retinoic acid in the developing chicken wing bud. When locally applied to the wing bud, S-4o9cDH-RA induced digit pattern duplications in a dose-dependent fashion. The results illustrate that S-4o9cDH-RA closely mimics all-trans-retinoic acid with regard to pattern respecification. Finally, using quantitative RT-PCR analysis, we showed that S-4o9cDH-RA induces the transcription of several retinoic acid-regulated genes in chick wing buds, including Hoxb8, RARβ2, shh, Cyp26 and bmp2. Although S-4o9cDH-RA was less potent when compared with all-trans-retinoic acid, the findings clearly demonstrate that S-4o9cDH-RA has the capacity to bind and activate nuclear retinoid receptors and regulate gene transcription both in vitro and in vivo.</description><identifier>ISSN: 1742-464X</identifier><identifier>ISSN: 1742-4658</identifier><identifier>EISSN: 1742-4658</identifier><identifier>DOI: 10.1111/j.1742-4658.2009.07023.x</identifier><identifier>PMID: 19490107</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Acids ; Animals ; Biochemistry ; Birds ; Cell Line ; Cell Line, Tumor ; Chick Embryo ; Chickens ; dihydro-retinoic acid metabolite ; Electrophoresis, Polyacrylamide Gel ; gene expression ; Gene Expression - drug effects ; Genetics ; HeLa Cells ; Humans ; Limb Buds - drug effects ; Limb Buds - metabolism ; Luciferases - genetics ; Luciferases - metabolism ; Medicin och hälsovetenskap ; Metabolites ; Mice ; Molecular Structure ; novel retinoid metabolites ; Promoter Regions, Genetic - genetics ; RAR ; Rats ; Receptors, Retinoic Acid - genetics ; Receptors, Retinoic Acid - metabolism ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - metabolism ; Retinoic Acid Receptor alpha ; Rodents ; Signal Transduction - drug effects ; Signal Transduction - physiology ; Transfection ; Tretinoin - analogs & derivatives ; Tretinoin - chemistry ; Tretinoin - metabolism ; Tretinoin - pharmacology ; vitamin A metabolism ; Wings, Animal - drug effects ; Wings, Animal - embryology</subject><ispartof>The FEBS journal, 2009-06, Vol.276 (11), p.3043-3059</ispartof><rights>2009 The Authors Journal compilation © 2009 FEBS</rights><rights>Journal compilation © 2009 Federation of European Biochemical Societies</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5573-6b2955b1bacc73d711590d6e685f9662b761b7928900e004f98132e06b6fc3e63</citedby><cites>FETCH-LOGICAL-c5573-6b2955b1bacc73d711590d6e685f9662b761b7928900e004f98132e06b6fc3e63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1742-4658.2009.07023.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1742-4658.2009.07023.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,315,781,785,886,1418,1434,27928,27929,45578,45579,46413,46837</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19490107$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:118744042$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Schuchardt, Jan P</creatorcontrib><creatorcontrib>Wahlström, David</creatorcontrib><creatorcontrib>Rüegg, Joëlle</creatorcontrib><creatorcontrib>Giese, Norbert</creatorcontrib><creatorcontrib>Stefan, Madalina</creatorcontrib><creatorcontrib>Hopf, Henning</creatorcontrib><creatorcontrib>Pongratz, Ingemar</creatorcontrib><creatorcontrib>Håkansson, Helen</creatorcontrib><creatorcontrib>Eichele, Gregor</creatorcontrib><creatorcontrib>Pettersson, Katarina</creatorcontrib><creatorcontrib>Nau, Heinz</creatorcontrib><title>endogenous retinoid metabolite S-4-oxo-9-cis-13,14-dihydro-retinoic acid activates retinoic acid receptor signalling both in vitro and in vivo</title><title>The FEBS journal</title><addtitle>FEBS J</addtitle><description>Retinoic acid receptor (RAR) and retinoid X receptor are ligand-induced transcription factors that belong to the nuclear receptor family. The receptors are activated by small hydrophobic compounds, such as all-trans-retinoic acid and 9-cis-retinoic acid, respectively. Interestingly, these receptors are also targets for a number of exogenous compounds. In this study, we characterized the biological activity of the 9-cis-substituted retinoic acid metabolite, S-4-oxo-9-cis-13,14-dihydro-retinoic acid (S-4o9cDH-RA). The endogenous levels of this metabolite in wild-type mice and rats were found to be higher than those of all-trans-retinoic acid, especially in the liver. Using cell-based luciferase reporter systems, we showed that S-4o9cDH-RA activates the transcription of retinoic acid response element-containing genes in several cell types, both from a simple 2xDR5 element and from the promoter of the natural retinoid target gene RARβ2. In addition, quantitative RT-PCR analysis demonstrated that S-4o9cDH-RA treatment significantly increases the endogenous mRNA levels of the RAR target gene RARβ2. Utilizing a limited proteolytic digestion assay, we showed that S-4o9cDH-RA induces conformational changes to both RARα and RARβ in the same manner as does all-trans-retinoic acid, suggesting that S-4o9cDH-RA is indeed an endogenous ligand for these receptors. These in vitro results were corroborated in an in vivo system, where S-4o9cDH-RA induced morphological changes similar to those of all-trans-retinoic acid in the developing chicken wing bud. When locally applied to the wing bud, S-4o9cDH-RA induced digit pattern duplications in a dose-dependent fashion. The results illustrate that S-4o9cDH-RA closely mimics all-trans-retinoic acid with regard to pattern respecification. Finally, using quantitative RT-PCR analysis, we showed that S-4o9cDH-RA induces the transcription of several retinoic acid-regulated genes in chick wing buds, including Hoxb8, RARβ2, shh, Cyp26 and bmp2. Although S-4o9cDH-RA was less potent when compared with all-trans-retinoic acid, the findings clearly demonstrate that S-4o9cDH-RA has the capacity to bind and activate nuclear retinoid receptors and regulate gene transcription both in vitro and in vivo.</description><subject>Acids</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Birds</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>Chick Embryo</subject><subject>Chickens</subject><subject>dihydro-retinoic acid metabolite</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>gene expression</subject><subject>Gene Expression - drug effects</subject><subject>Genetics</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Limb Buds - drug effects</subject><subject>Limb Buds - metabolism</subject><subject>Luciferases - genetics</subject><subject>Luciferases - metabolism</subject><subject>Medicin och hälsovetenskap</subject><subject>Metabolites</subject><subject>Mice</subject><subject>Molecular Structure</subject><subject>novel retinoid metabolites</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>RAR</subject><subject>Rats</subject><subject>Receptors, Retinoic Acid - genetics</subject><subject>Receptors, Retinoic Acid - metabolism</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Retinoic Acid Receptor alpha</subject><subject>Rodents</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - physiology</subject><subject>Transfection</subject><subject>Tretinoin - analogs & derivatives</subject><subject>Tretinoin - chemistry</subject><subject>Tretinoin - metabolism</subject><subject>Tretinoin - pharmacology</subject><subject>vitamin A metabolism</subject><subject>Wings, Animal - drug effects</subject><subject>Wings, Animal - embryology</subject><issn>1742-464X</issn><issn>1742-4658</issn><issn>1742-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks1u1DAUhSMEoqXwChCxYIUH_zveIJWqBaRKLEoldpbj3Ew9ZOLBzkxnXoJnxiFhKiEh4Y2vr79zbNmnKEqCFySPd6sFUZwiLkW1oBjrBVaYssX-UXF63Hh8rPm3k-JZSiuMmeBaPy1OiOYaE6xOi5_QN2EJfdimMsLg--Cbcg2DrUPnByhvEEdhH5BGzidE2FvCUePvDk0MaOZdaV0WWTf4nR3g6DP3IzjYDCGWyS9723W-X5Z1GO5K35c7P8RQ2r6ZFrvwvHjS2i7Bi3k-K26vLr9efELXXz5-vji_Rk4IxZCsqRaiJrV1TrFGESI0biTISrRaSlorSWqlaaUxBox5qyvCKGBZy9YxkOysQJNvuofNtjab6Nc2Hkyw3syt77kCk49Tosq8_ie_iaF5EP0RElIpzjGnWftm0mbwxxbSYNY-Oeg620N-diMVI1KI8VKv_wJXYRvzmyVDMSdUKsozVE2QiyGlCO3xLgSbMRxmZcZ_N2MGzBgO8zscZp-lL2f_bb2G5kE4pyED7yfg3ndw-G9jc3X54WYss8GryaC1wdhl9Mnc3lBMGCaSKokF-wXrENLA</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>Schuchardt, Jan P</creator><creator>Wahlström, David</creator><creator>Rüegg, Joëlle</creator><creator>Giese, Norbert</creator><creator>Stefan, Madalina</creator><creator>Hopf, Henning</creator><creator>Pongratz, Ingemar</creator><creator>Håkansson, Helen</creator><creator>Eichele, Gregor</creator><creator>Pettersson, Katarina</creator><creator>Nau, Heinz</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>200906</creationdate><title>endogenous retinoid metabolite S-4-oxo-9-cis-13,14-dihydro-retinoic acid activates retinoic acid receptor signalling both in vitro and in vivo</title><author>Schuchardt, Jan P ; Wahlström, David ; Rüegg, Joëlle ; Giese, Norbert ; Stefan, Madalina ; Hopf, Henning ; Pongratz, Ingemar ; Håkansson, Helen ; Eichele, Gregor ; Pettersson, Katarina ; Nau, Heinz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5573-6b2955b1bacc73d711590d6e685f9662b761b7928900e004f98132e06b6fc3e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acids</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Birds</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>Chick Embryo</topic><topic>Chickens</topic><topic>dihydro-retinoic acid metabolite</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>gene expression</topic><topic>Gene Expression - drug effects</topic><topic>Genetics</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Limb Buds - drug effects</topic><topic>Limb Buds - metabolism</topic><topic>Luciferases - genetics</topic><topic>Luciferases - metabolism</topic><topic>Medicin och hälsovetenskap</topic><topic>Metabolites</topic><topic>Mice</topic><topic>Molecular Structure</topic><topic>novel retinoid metabolites</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>RAR</topic><topic>Rats</topic><topic>Receptors, Retinoic Acid - genetics</topic><topic>Receptors, Retinoic Acid - metabolism</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Retinoic Acid Receptor alpha</topic><topic>Rodents</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - physiology</topic><topic>Transfection</topic><topic>Tretinoin - analogs & derivatives</topic><topic>Tretinoin - chemistry</topic><topic>Tretinoin - metabolism</topic><topic>Tretinoin - pharmacology</topic><topic>vitamin A metabolism</topic><topic>Wings, Animal - drug effects</topic><topic>Wings, Animal - embryology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schuchardt, Jan P</creatorcontrib><creatorcontrib>Wahlström, David</creatorcontrib><creatorcontrib>Rüegg, Joëlle</creatorcontrib><creatorcontrib>Giese, Norbert</creatorcontrib><creatorcontrib>Stefan, Madalina</creatorcontrib><creatorcontrib>Hopf, Henning</creatorcontrib><creatorcontrib>Pongratz, Ingemar</creatorcontrib><creatorcontrib>Håkansson, Helen</creatorcontrib><creatorcontrib>Eichele, Gregor</creatorcontrib><creatorcontrib>Pettersson, Katarina</creatorcontrib><creatorcontrib>Nau, Heinz</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>The FEBS journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schuchardt, Jan P</au><au>Wahlström, David</au><au>Rüegg, Joëlle</au><au>Giese, Norbert</au><au>Stefan, Madalina</au><au>Hopf, Henning</au><au>Pongratz, Ingemar</au><au>Håkansson, Helen</au><au>Eichele, Gregor</au><au>Pettersson, Katarina</au><au>Nau, Heinz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>endogenous retinoid metabolite S-4-oxo-9-cis-13,14-dihydro-retinoic acid activates retinoic acid receptor signalling both in vitro and in vivo</atitle><jtitle>The FEBS journal</jtitle><addtitle>FEBS J</addtitle><date>2009-06</date><risdate>2009</risdate><volume>276</volume><issue>11</issue><spage>3043</spage><epage>3059</epage><pages>3043-3059</pages><issn>1742-464X</issn><issn>1742-4658</issn><eissn>1742-4658</eissn><abstract>Retinoic acid receptor (RAR) and retinoid X receptor are ligand-induced transcription factors that belong to the nuclear receptor family. The receptors are activated by small hydrophobic compounds, such as all-trans-retinoic acid and 9-cis-retinoic acid, respectively. Interestingly, these receptors are also targets for a number of exogenous compounds. In this study, we characterized the biological activity of the 9-cis-substituted retinoic acid metabolite, S-4-oxo-9-cis-13,14-dihydro-retinoic acid (S-4o9cDH-RA). The endogenous levels of this metabolite in wild-type mice and rats were found to be higher than those of all-trans-retinoic acid, especially in the liver. Using cell-based luciferase reporter systems, we showed that S-4o9cDH-RA activates the transcription of retinoic acid response element-containing genes in several cell types, both from a simple 2xDR5 element and from the promoter of the natural retinoid target gene RARβ2. In addition, quantitative RT-PCR analysis demonstrated that S-4o9cDH-RA treatment significantly increases the endogenous mRNA levels of the RAR target gene RARβ2. Utilizing a limited proteolytic digestion assay, we showed that S-4o9cDH-RA induces conformational changes to both RARα and RARβ in the same manner as does all-trans-retinoic acid, suggesting that S-4o9cDH-RA is indeed an endogenous ligand for these receptors. These in vitro results were corroborated in an in vivo system, where S-4o9cDH-RA induced morphological changes similar to those of all-trans-retinoic acid in the developing chicken wing bud. When locally applied to the wing bud, S-4o9cDH-RA induced digit pattern duplications in a dose-dependent fashion. The results illustrate that S-4o9cDH-RA closely mimics all-trans-retinoic acid with regard to pattern respecification. Finally, using quantitative RT-PCR analysis, we showed that S-4o9cDH-RA induces the transcription of several retinoic acid-regulated genes in chick wing buds, including Hoxb8, RARβ2, shh, Cyp26 and bmp2. Although S-4o9cDH-RA was less potent when compared with all-trans-retinoic acid, the findings clearly demonstrate that S-4o9cDH-RA has the capacity to bind and activate nuclear retinoid receptors and regulate gene transcription both in vitro and in vivo.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>19490107</pmid><doi>10.1111/j.1742-4658.2009.07023.x</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acids Animals Biochemistry Birds Cell Line Cell Line, Tumor Chick Embryo Chickens dihydro-retinoic acid metabolite Electrophoresis, Polyacrylamide Gel gene expression Gene Expression - drug effects Genetics HeLa Cells Humans Limb Buds - drug effects Limb Buds - metabolism Luciferases - genetics Luciferases - metabolism Medicin och hälsovetenskap Metabolites Mice Molecular Structure novel retinoid metabolites Promoter Regions, Genetic - genetics RAR Rats Receptors, Retinoic Acid - genetics Receptors, Retinoic Acid - metabolism Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - metabolism Retinoic Acid Receptor alpha Rodents Signal Transduction - drug effects Signal Transduction - physiology Transfection Tretinoin - analogs & derivatives Tretinoin - chemistry Tretinoin - metabolism Tretinoin - pharmacology vitamin A metabolism Wings, Animal - drug effects Wings, Animal - embryology |
title | endogenous retinoid metabolite S-4-oxo-9-cis-13,14-dihydro-retinoic acid activates retinoic acid receptor signalling both in vitro and in vivo |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-16T19%3A46%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=endogenous%20retinoid%20metabolite%20S-4-oxo-9-cis-13,14-dihydro-retinoic%20acid%20activates%20retinoic%20acid%20receptor%20signalling%20both%20in%20vitro%20and%20in%20vivo&rft.jtitle=The%20FEBS%20journal&rft.au=Schuchardt,%20Jan%20P&rft.date=2009-06&rft.volume=276&rft.issue=11&rft.spage=3043&rft.epage=3059&rft.pages=3043-3059&rft.issn=1742-464X&rft.eissn=1742-4658&rft_id=info:doi/10.1111/j.1742-4658.2009.07023.x&rft_dat=%3Cproquest_swepu%3E67316556%3C/proquest_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=204126724&rft_id=info:pmid/19490107&rfr_iscdi=true |