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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.jprot.2012.07.001</dc:identifier><dc:language>eng</dc:language><dc:creator>Ramírez-Torres, A</dc:creator><dc:creator>Barceló-Batllori, S</dc:creator><dc:creator>Martínez-Beamonte, R</dc:creator><dc:creator>Navarro, MA</dc:creator><dc:creator>Surra, JC</dc:creator><dc:creator>Arnal, C</dc:creator><dc:creator>Guillén, N</dc:creator><dc:creator>Acín, S</dc:creator><dc:creator>Osada, J</dc:creator><dc:title>Proteomics and gene expression analyses of squalene-supplemented mice identify microsomal thioredoxin domain-containing protein 5 changes associated with hepatic steatosis</dc:title><dc:identifier>ART-2012-79132</dc:identifier><dc:description>Squalene is an abundant hydrocarbon present in virgin olive oil. Previous studies showed that its administration decreased atherosclerosis and steatosis in male apoE-knock-out mice. To study its effects on microsomal proteins, 1 g/kg/day of squalene was administered to those mice. After 10 weeks, hepatic fat content was assessed and protein extracts of microsomal enriched fractions from control and squalene-treated animals were analyzed by 2D-DIGE. Spots exhibiting significant differences were identified by peptide fingerprinting and MSMS analysis. Squalene administration modified the expression of thirty-one proteins involved in different metabolic functions and increased the levels of those involved in vesicle transport, protein folding and redox status. Only mRNA levels of 9 genes (Arg1, Atp5b, Cat, Hyou1, Nipsnap1, Pcca, Pcx, Pyroxd2, and Txndc5) paralleled these findings. No such mRNA changes were observed in wild-type mice receiving squalene. Thioredoxin domain-containing protein 5 (TXNDC5) protein and mRNA levels were significantly associated with hepatic fat content in apoE-ko mice. These results suggest that squalene action may be executed through a complex regulation of microsomal proteins, both at the mRNA and post-transcriptional levels and the presence of apoE may change the outcome. Txndc5 reflects the anti-steatotic properties of squalene and the sensitivity to lipid accumulation.</dc:description><dc:date>2012</dc:date><dc:source>http://zaguan.unizar.es/record/129992</dc:source><dc:doi>10.1016/j.jprot.2012.07.001</dc:doi><dc:identifier>http://zaguan.unizar.es/record/129992</dc:identifier><dc:identifier>oai:zaguan.unizar.es:129992</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/CICYT-FEDER/SAF 2010-14958</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA-FSE/B69</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA/PI025-08</dc:relation><dc:identifier.citation>JOURNAL OF PROTEOMICS 77 (2012), 27-39</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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