Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor

被引:9
|
作者
Yoon, Ye Ran [1 ]
Lee, Tae-Gul [1 ]
Choi, Mi-Hyun [1 ]
Shin, Seung Woo [1 ]
Ko, Young-Gyu [1 ]
Rhyu, Im Joo [2 ,3 ]
Kim, Dong-Hoon [3 ,4 ]
Seong, Je Kyung [5 ,6 ,7 ,8 ,9 ]
Baik, Ja-Hyun [1 ,3 ]
机构
[1] Korea Univ, Dept Life Sci, Seoul 02841, South Korea
[2] Korea Univ, Dept Anat, Coll Med, Seoul 02841, South Korea
[3] Korea Univ, Dept Med Sci, Coll Med, Seoul 02841, South Korea
[4] Korea Univ, Dept Pharmacol, Coll Med, Seoul 02841, South Korea
[5] Seoul Natl Univ, Coll Vet Med, Lab Dev Biol & Genom, Inst Vet Sci, Seoul, South Korea
[6] Seoul Natl Univ, Coll Vet Med, Program Vet Sci BK21, Seoul, South Korea
[7] Seoul Natl Univ, KMPC, Seoul, South Korea
[8] Seoul Natl Univ, Interdisciplinary Program Bioinformat, Program Canc Biol, Seoul, South Korea
[9] Seoul Natl Univ, Bio MAX Inst, Seoul, South Korea
来源
基金
新加坡国家研究基金会;
关键词
ENDOPLASMIC-RETICULUM STRESS; CELL-SURFACE EXPRESSION; ENERGY HOMEOSTASIS; ER STRESS; CONSTITUTIVE ACTIVITY; CHEMICAL CHAPERONES; SUBSTRATE-BINDING; PEPTIDE BINDING; MOUSE MODEL; OBESITY;
D O I
10.1038/s12276-018-0144-8
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
The melanocortin-4 receptor (MC4R) belongs to the G protein-coupled receptor (GPCR) family and plays an essential role in the control of energy homeostasis. Here, we identified a novel MC4R-interacting protein, glucose-regulated protein 78 (GRP78), from a pulldown assay using hypothalamic protein extracts and the third intracellular loop of MC4R. We found that MC4R interacted with GRP78 in both the cytosol and at the cell surface and that this interaction increased when MC4R was internalized in the presence of the agonist melanotan-II (MTII). Downregulation of GRP78 using a short interfering RNA approach attenuated MTII-mediated receptor internalization. Reduction in GRP78 expression during tunicamycin-induced endoplasmic reticulum stress also suppressed MTII-mediated internalization of MC4R and cAMP-mediated transcriptional activity. Furthermore, lentiviral-mediated short hairpin RNA knockdown of endogenous GRP78 in the paraventricular nucleus (PVN) of the hypothalamus resulted in an increase in body weight in mice fed a high-fat diet. These results suggest that GRP78 in the PVN binds to MC4R and may have a chaperone-like role in the regulation of MC4R trafficking and signaling.
引用
收藏
页码:1 / 14
页数:14
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