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星形胶质细胞上调基因1(AEG-1)调节脂质稳态。

Astrocyte Elevated Gene-1 (AEG-1) Regulates Lipid Homeostasis.

作者信息

Robertson Chadia L, Srivastava Jyoti, Siddiq Ayesha, Gredler Rachel, Emdad Luni, Rajasekaran Devaraja, Akiel Maaged, Shen Xue-Ning, Corwin Frank, Sundaresan Gobalakrishnan, Zweit Jamal, Croniger Colleen, Gao Xiaoli, Ghosh Shobha, Hylemon Philip B, Subler Mark A, Windle Jolene J, Fisher Paul B, Sarkar Devanand

机构信息

Departments of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, Virginia 23298; Departments of Biochemistry, Virginia Commonwealth University, Richmond, Virginia 23298.

Departments of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, Virginia 23298.

出版信息

J Biol Chem. 2015 Jul 17;290(29):18227-18236. doi: 10.1074/jbc.M115.661801. Epub 2015 Jun 11.

Abstract

Astrocyte elevated gene-1 (AEG-1), also known as MTDH (metadherin) or LYRIC, is an established oncogene. However, the physiological function of AEG-1 is not known. To address this question, we generated an AEG-1 knock-out mouse (AEG-1KO) and characterized it. Although AEG-1KO mice were viable and fertile, they were significantly leaner with prominently less body fat and lived significantly longer compared with wild type (WT). When fed a high fat and cholesterol diet (HFD), WT mice rapidly gained weight, whereas AEG-1KO mice did not gain weight at all. This phenotype of AEG-1KO mice is due to decreased fat absorption from the intestines, not because of decreased fat synthesis or increased fat consumption. AEG-1 interacts with retinoid X receptor (RXR) and inhibits RXR function. In enterocytes of AEG-1KO mice, we observed increased activity of RXR heterodimer partners, liver X receptor and peroxisome proliferator-activated receptor-α, key inhibitors of intestinal fat absorption. Inhibition of fat absorption in AEG-1KO mice was further augmented when fed an HFD providing ligands to liver X receptor and peroxisome proliferator-activated receptor-α. Our studies reveal a novel role of AEG-1 in regulating nuclear receptors controlling lipid metabolism. AEG-1 may significantly modulate the effects of HFD and thereby function as a unique determinant of obesity.

摘要

星形胶质细胞上调基因1(AEG-1),也被称为MTDH(黏附素)或LYRIC,是一种公认的癌基因。然而,AEG-1的生理功能尚不清楚。为了解决这个问题,我们构建了一只AEG-1敲除小鼠(AEG-1KO)并对其进行了特征描述。尽管AEG-1KO小鼠能够存活且可育,但与野生型(WT)相比,它们明显更瘦,体脂显著减少,寿命也显著更长。当喂食高脂肪高胆固醇饮食(HFD)时,WT小鼠体重迅速增加,而AEG-1KO小鼠根本没有体重增加。AEG-1KO小鼠的这种表型是由于肠道脂肪吸收减少,而不是因为脂肪合成减少或脂肪消耗增加。AEG-1与视黄酸X受体(RXR)相互作用并抑制RXR功能。在AEG-1KO小鼠的肠细胞中,我们观察到RXR异二聚体伴侣、肝脏X受体和过氧化物酶体增殖物激活受体-α(肠道脂肪吸收的关键抑制剂)的活性增加。当喂食能为肝脏X受体和过氧化物酶体增殖物激活受体-α提供配体的HFD时,AEG-1KO小鼠的脂肪吸收抑制作用进一步增强。我们的研究揭示了AEG-1在调节控制脂质代谢的核受体方面的新作用。AEG-1可能会显著调节HFD的影响,从而作为肥胖的一个独特决定因素发挥作用。

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