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Enzymatically modified low-density lipoprotein upregulates CD36 in low-differentiated monocytic cells in a peroxisome proliferator-activated receptor-gamma-dependent way

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    SYSNO ASEP0105319
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleEnzymatically modified low-density lipoprotein upregulates CD36 in low-differentiated monocytic cells in a peroxisome proliferator-activated receptor-gamma-dependent way
    TitleEnzymaticky modifikovaný lipoprotein o nízké hustotě (LDL) zvyšuje expresi CD36 v málo diferencovaných monocytech cestou závislou na receptoru gama aktivovaném peroxizomových proliferátorem
    Author(s) Jostarndt, K. (DE)
    Rubic, T. (DE)
    Kuhn, H. (DE)
    Anthosen, M. W. (NO)
    Anděra, Ladislav (MBU-M)
    Gellert, N. (DE)
    Trottman, M. (DE)
    Weber, C. (DE)
    Johansen, B. (NO)
    Hrboticky, N. (DE)
    Neuzil, J. (AU)
    Source TitleBiochemical Pharmacology. - : Elsevier - ISSN 0006-2952
    Roč. 67, - (2004), s. 841-854
    Number of pages14 s.
    Languageeng - English
    CountryUS - United States
    KeywordsPPARg, CD36, LDL
    Subject RIVEB - Genetics ; Molecular Biology
    CEZAV0Z5052915 - UMG-J
    AnnotationPeroxisome proliferator-activated receptor-g (PPARg) has been suggested to upregulate CD36. Since free oxidized polyunsaturated fatty acids are PPARg ligands, we studied the effects of LDL modified by the simultaneous action of sPLA2 and 15-lipoxygenase (15LO) on CD36 expression and PPARg activation in monocytic cells. Exposure of MM6 cells, which do not express CD36 or other scavenger receptors, to such enzymatically modified LDL (enzLDL) resulted in upregulation of CD36 surface protein and mRNA expression. Similar effects were observed with free 13-hydroperoxyoctadecadienoic acid but not its esterified counterpart. Less pronounced effects were observed with LDL modified by 15LO alone. Upregulation of CD36 was inversely correlated to the state of cell differentiation, as showed by lower response to enzLDL of the scavenger receptor-expressing MM6-sr and THP1 cells. Importantly, LDL modified by sPLA2 and 15LO did not efficiently induce upregulation CD36 in PPARg-deficient macrophage-differentiated embryonic stem cells confirming a role of PPARg in CD36 expression in cells stimulated with enzLDL. Our data show that LDL modified with physiologically relevant enzymes stimulates CD36 expression in non-differentiated monocytes and that this process involves PPARg activation. These effects of enzLDL can be considered pro-atherogenic in the context of early atherosclerosis
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2005

Number of the records: 1  

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