The Melanocortin Receptor Accessory Protein 2 promotes food intake through inhibition of the Prokineticin Receptor-1

被引:65
作者
Chaly, Anna L. [1 ,2 ,3 ]
Srisai, Dollada [1 ,2 ,3 ]
Gardner, Ellen E. [1 ,2 ,3 ]
Sebag, Julien A. [1 ,2 ,3 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Mol Physiol & Biophys, Iowa City, IA USA
[2] Univ Iowa, Pappajohn Biomed Inst, Iowa City, IA USA
[3] Univ Iowa, Fraternal Order Eagle Diabet Res Ctr, Iowa City, IA USA
关键词
FUNCTIONAL EXPRESSION; COUPLED RECEPTORS; MRAP; TRAFFICKING; FAMILY; IDENTIFICATION; MODULATORS; KNOCKOUT; RAMPS; MC2;
D O I
10.7554/eLife.12397
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Melanocortin Receptor Accessory Protein 2 (MRAP2) is an important regulator of energy homeostasis and its loss causes severe obesity in rodents. MRAP2 mediates its action in part through the potentiation of the MC4R, however, it is clear that MRAP2 is expressed in tissues that do not express MC4R, and that the deletion of MRAP2 does not recapitulate the phenotype of Mc4r KO mice. Consequently, we hypothesized that other GPCRs involved in the control of energy homeostasis are likely to be regulated by MRAP2. In this study we identified PKR1 as the first nonmelanocortin GPCR to be regulated by MRAP2. We show that MRAP2 significantly and specifically inhibits PKR1 signaling. We also demonstrate that PKR1 and MRAP2 co-localize in neurons and that Mrap2 KO mice are hypersensitive to PKR1 stimulation. This study not only identifies new partners of MRAP2 but also a new pathway through which MRAP2 regulates energy homeostasis.
引用
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页数:17
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