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Trans-10, cis-12 conjugated linoleic acid activates the integrated stress response pathway in adipocytes.

Trans-10, cis-12 conjugated linoleic acid activates the integrated stress response pathway in adipocytes. Research Abstract Details 

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  • Trans-10, cis-12 conjugated linoleic acid activates the integrated stress response pathway in adipocytes. Abstract Text:

    p christopher larosaP Christopher LaRosa,jean-jack m riethovenJean-Jack M Riethoven,han chenHan Chen,yuannan xiaYuannan Xia,you zhouYou Zhou,mei chenMei Chen,jess minerJess Miner,michael e frommMichael E Fromm,p christopher larosaP Christopher LaRosa,jean-jack m riethovenJean-Jack M Riethoven,han chenHan Chen,yuannan xiaYuannan Xia,you zhouYou Zhou,mei chenMei Chen,jess minerJess Miner,michael e frommMichael E Fromm,p christopher larosaP Christopher LaRosa,jean-jack m riethovenJean-Jack M Riethoven,han chenHan Chen,yuannan xiaYuannan Xia,you zhouYou Zhou,mei chenMei Chen,jess minerJess Miner,michael e frommMichael E Fromm,

    Trans-10, cis-12 conjugated linoleic acid (t10c12 CLA) causes fat loss in mouse white adipose tissue (WAT) and adipocytes in culture. The early transcriptome changes in treated WAT and 3T3-L1 adipocytes were analyzed using high-density microarrays to better characterize the signaling pathways responding to t10c12 CLA. Gene expression responses between 4 and 24 h after treatment showed a common set of early gene expression changes indicative of an integrated stress response (ISR). The responses of 3T3-L1 preadipocytes treated with t10c12 CLA or adipocytes treated with the cis-9, trans-11 isomer of CLA did not show the ISR, indicating the effect is specific to adipocytes responding to t10c12 CLA. Western blot analysis found increased phosphorylation of eIF2 alpha and increased production of ATF4 confirming at least part of the response to t10c12 CLA is mediated through the ISR pathway. Immunofluorescence microscopy found that the cell type expressing ATF3, an indicator of the ISR, was early stage adipocytes containing oil droplets but lacking the abundant levels of fatty acid binding protein-4 (FABP4) (AP2) found in mature adipocytes. Our data suggests that the ISR precedes and is possibly the cause of the later induction of proinflammatory cytokines observed in t10c12 CLA treated adipocytes. The release of proinflammatory cytokines may explain how the ISR in early stage adipocytes causes lipid loss in mature adipocytes.

    Trans-10, cis-12 conjugated linoleic acid activates the integrated stress response pathway in adipocytes. Publishing Authors By Initials

    pc larosaPC LaRosa,jj riethovenJJ Riethoven,h chenH Chen,y xiaY Xia,y zhouY Zhou,m chenM Chen,j minerJ Miner,me frommME Fromm,pc larosaPC LaRosa,jj riethovenJJ Riethoven,h chenH Chen,y xiaY Xia,y zhouY Zhou,m chenM Chen,j minerJ Miner,me frommME Fromm,pc larosaPC LaRosa,jj riethovenJJ Riethoven,h chenH Chen,y xiaY Xia,y zhouY Zhou,m chenM Chen,j minerJ Miner,me frommME Fromm,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

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    Trans-10, cis-12 conjugated linoleic acid activates the integrated stress response pathway in adipocytes. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Physiological genomics

    VOLUME: 31

    Page Numbers: 544-53

    Journal Abbreviation: Physiol. Genomics

    ISSN: 1531-2267

    DAY: 18

    MONTH: 09

    YEAR: 2007

    Trans-10, cis-12 conjugated linoleic acid activates the integrated stress response pathway in adipocytes. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9815683

    Trans-10, cis-12 conjugated linoleic acid activates the integrated stress response pathway in adipocytes. Keywords Mesh Terms:

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    Grant and Affiliation Information for Trans-10, cis-12 conjugated linoleic acid activates the integrated stress response pathway in adipocytes.

    AFFILIATION: Center for Biotechnology, University of Nebraska, Lincoln, Nebraska 68588-0665, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Physiol Genomics

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