人载脂蛋白A-II转基因小鼠血浆对J774巨噬细胞和Fu5AH肝癌细胞胆固醇外排的相反作用

N. Fournier, A. Cogny, V. Atger, D. Pastier, D. Goudounèche, A. Nicoletti, N. Moatti, J. Chambaz, J. Paul, A. Kalopissis
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引用次数: 37

摘要

在转基因小鼠(hAIItg小鼠)中,人载脂蛋白a - ii (hapo a - ii)的过度表达诱导了显著的高甘油三酯血症和低水平的血浆高密度脂蛋白(HDL)(高hapo a - ii含量)。我们试图确定这些小鼠的血浆和高密度脂蛋白胆固醇外排是否会受到影响。在Fu5AH细胞系统中,来自hAIItg小鼠的血浆诱导的胆固醇外排明显低于对照血浆,这与外排对HDL浓度的依赖性一致。此外,来自hAIItg小鼠的hdl受体不如对照hdl受体有效。在J774巨噬细胞系统中,预处理cAMP可上调ATP结合盒转运蛋白1,诱导haitg血浆外排明显增加,并纯化hapo a - i和hapo a - ii,而对控制血浆的胆固醇外排无影响。外排cAMP刺激百分比与血浆hapo A- ii浓度呈正相关。cAMP对小鼠血浆外排的刺激可能与pre- bgr的存在有关。迁移HDL含有hapo A-II。因此,尽管高密度脂蛋白和载脂蛋白A-I含量较低,但hAIItg小鼠血浆从巨噬细胞样细胞中提取胆固醇的能力增加可能具有抗动脉粥样硬化的作用。
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Opposite Effects of Plasma From Human Apolipoprotein A-II Transgenic Mice on Cholesterol Efflux From J774 Macrophages and Fu5AH Hepatoma Cells
Overexpression of human apolipoprotein A-II (hapo A-II) in transgenic mice (hAIItg mice) induced marked hypertriglyceridemia and low levels of plasma high density lipoprotein (HDL) with a high hapo A-II content. We sought to determine whether cholesterol efflux to plasma and HDL from these mice would be affected. In the Fu5AH cell system, plasma from hAIItg mice induced a markedly lower cholesterol efflux than did control plasma, in accordance with the dependence of efflux on HDL concentration. Moreover, HDLs from hAIItg mice were less effective acceptors than were control HDLs. In the J774 macrophage cell system, pretreatment with cAMP, which upregulates ATP binding cassette transporter 1, induced a marked increase in the efflux to hAIItg plasma as well as to purified hapo A-I and hapo A-II, whereas it had no effect on cholesterol efflux to control plasma. A strong positive correlation was established between percent cAMP stimulation of efflux and plasma hapo A-II concentration. The cAMP stimulation of efflux to hAIItg mouse plasma may be linked to the presence of pre-&bgr; migrating HDL containing hapo A-II. Thus, despite lower HDL and apolipoprotein A-I contents, the increased ability of plasma from hAIItg mice to extract cholesterol from macrophage-like cells may have an antiatherogenic influence.
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