Yang Chendong, Yu Liqing, Li Weiping, Xu Fang, Cohen Jonathan C, Hobbs Helen H
Department of Molecular Genetics, McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas 75390-9046, USA.
J Clin Invest. 2004 Sep;114(6):813-22. doi: 10.1172/JCI22186.
The ABC transporters ABCG5 and ABCG8 limit absorption and promote excretion of dietary plant sterols. It is not known why plant sterols are so assiduously excluded from the body. Here we show that accumulation of plant sterols in mice lacking ABCG5 and ABCG8 (G5G8-/- mice) profoundly perturbs cholesterol homeostasis in the adrenal gland. The adrenal glands of the G5G8-/- mice were grossly abnormal in appearance (brown, not white) due to a 91% reduction in cholesterol content. Despite the very low cholesterol levels, there was no compensatory increase in cholesterol synthesis or in lipoprotein receptor expression. Moreover, levels of ABCA1, which mediates sterol efflux, were increased 10-fold in the G5G8-/- adrenals. Adrenal cholesterol levels returned to near-normal levels in mice treated with ezetimibe, which blocks phytosterol absorption. To determine which plant sterol(s) caused the metabolic changes, we examined the effects of individual plant sterols on cholesterol metabolism in cultured adrenal cells. Addition of stigmasterol, but not sitosterol, inhibited SREBP-2 processing and reduced cholesterol synthesis. Stigmasterol also activated the liver X receptor in a cell-based reporter assay. These data indicate that selected dietary plant sterols disrupt cholesterol homeostasis by affecting two critical regulatory pathways of lipid metabolism.
ABC转运蛋白ABCG5和ABCG8限制膳食植物甾醇的吸收并促进其排泄。目前尚不清楚为何植物甾醇会如此严格地被排除在体内。在此我们表明,缺乏ABCG5和ABCG8的小鼠(G5G8 - / - 小鼠)体内植物甾醇的积累严重扰乱了肾上腺中的胆固醇稳态。由于胆固醇含量降低了91%,G5G8 - / - 小鼠的肾上腺外观明显异常(呈褐色,而非白色)。尽管胆固醇水平极低,但胆固醇合成或脂蛋白受体表达并未出现代偿性增加。此外,介导甾醇流出的ABCA1水平在G5G8 - / - 肾上腺中增加了10倍。用依泽替米贝治疗的小鼠肾上腺胆固醇水平恢复到接近正常水平,依泽替米贝可阻断植物甾醇的吸收。为了确定是哪种植物甾醇导致了代谢变化,我们检测了单个植物甾醇对培养的肾上腺细胞中胆固醇代谢的影响。添加豆甾醇而非谷甾醇可抑制SREBP - 2的加工并减少胆固醇合成。在基于细胞的报告基因检测中,豆甾醇还激活了肝脏X受体。这些数据表明,特定的膳食植物甾醇通过影响脂质代谢的两个关键调节途径来破坏胆固醇稳态。