| Literature DB >> 26070567 |
Chadia L Robertson1, Jyoti Srivastava2, Ayesha Siddiq2, Rachel Gredler2, Luni Emdad2, Devaraja Rajasekaran2, Maaged Akiel2, Xue-Ning Shen2, Frank Corwin3, Gobalakrishnan Sundaresan3, Jamal Zweit3, Colleen Croniger4, Xiaoli Gao5, Shobha Ghosh6, Philip B Hylemon7, Mark A Subler2, Jolene J Windle8, Paul B Fisher9, Devanand Sarkar10.
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.Entities:
Keywords: gene regulation; intestine; lipid; liver metabolism; peroxisome proliferator-activated receptor (PPAR)
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Year: 2015 PMID: 26070567 PMCID: PMC4505065 DOI: 10.1074/jbc.M115.661801
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157