Lipoprotein Receptor LRP1 Regulates Leptin Signaling and Energy Homeostasis in the Adult Central Nervous System

被引:70
|
作者
Liu, Qiang [1 ]
Zhang, Juan [1 ]
Zerbinatti, Celina [1 ]
Zhan, Yan [1 ]
Kolber, Benedict J. [1 ]
Herz, Joachim [2 ]
Muglia, Louis J. [1 ]
Bu, Guojun [1 ,3 ,4 ,5 ]
机构
[1] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Mol Genet, Dallas, TX 75390 USA
[3] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
[4] Mayo Clin, Dept Neurosci, Jacksonville, FL 32224 USA
[5] Xiamen Univ, Inst Biomed Res, Xiamen, Peoples R China
基金
美国国家卫生研究院;
关键词
BRAIN APOLIPOPROTEIN-E; ALPHA-2-MACROGLOBULIN RECEPTOR; MELANOCORTIN SYSTEM; GENE KNOCKOUT; MOUSE-BRAIN; PROTEIN; EXPRESSION; BALANCE; MICE; NEURONS;
D O I
10.1371/journal.pbio.1000575
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Obesity is a growing epidemic characterized by excess fat storage in adipocytes. Although lipoprotein receptors play important roles in lipid uptake, their role in controlling food intake and obesity is not known. Here we show that the lipoprotein receptor LRP1 regulates leptin signaling and energy homeostasis. Conditional deletion of the Lrp1 gene in the brain resulted in an obese phenotype characterized by increased food intake, decreased energy consumption, and decreased leptin signaling. LRP1 directly binds to leptin and the leptin receptor complex and is required for leptin receptor phosphorylation and Stat3 activation. We further showed that deletion of the Lrp1 gene specifically in the hypothalamus by Cre lentivirus injection is sufficient to trigger accelerated weight gain. Together, our results demonstrate that the lipoprotein receptor LRP1, which is critical in lipid metabolism, also regulates food intake and energy homeostasis in the adult central nervous system.
引用
收藏
页数:9
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