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Oxidized Low-Density Lipoprotein Activates Adipophilin through Erk1/2 Signal Pathway in Raw264.7 Cells
SUNLONG BIOTECH / 2024-01-09
    • Type: RAW 264.7

    • Author:Liu, Q., Dai, Z., Liu, Z., Liu, X., Tang, C., Wang, Z., Yi, G., Liu, L., Jiang, Z., Yang, Y. & Yuan, Z.

    • Periodical:Acta biochimica et biophysica Sinica 42, 635-645 (2010)

    • Article source

    It has been reported that oxidized low-density lipoprotein (Ox-LDL) can increase the expression of adipophilin. However, the detailed mechanisms are not fully understood. The aim of this study was to investigate the mechanism of Ox-LDL on adipophilin expression and the intracellular lipid droplet accumulation. A mouse macrophage-like cell line, mouse-monocyte-macrophage-leukemia-cells , was used throughout, and it was found that Ox-LDL induced adipophilin expression in a dose-dependent manner. Moreover, Ox-LDL induced peroxisome proliferator-activated receptor-gamma (PPARgamma) expression and PPARgamma-specific inhibitor T0070907 abrogated Ox-LDL-induced adipophilin expression, but specific agonist GW1929 not. Furthermore, Ox-LDL induced phosphorylation of ERK1/2, and ERK1/2-specific inhibition by PD98059 suppressed the Ox-LDL-induced PPARgamma and adipophilin expression. The results showed that ERK1/2 or PPARgamma-specific inhibition decreased the amounts of intracellular lipid droplets. Meanwhile, the PPARgamma-specific agonist increased intracellular lipid droplets. These results suggested that Ox-LDL-induced increase in adipophilin level via ERK1/2 activation is one of the mechanisms of inducing greater amounts of intracellular lipid droplets in mouse-monocyte-macrophage-leukemia-cells cells, which indicated that adipophilin is involved in atherosclerotic progression.

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