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Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor
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 ex...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135830/ https://www.ncbi.nlm.nih.gov/pubmed/30209265 http://dx.doi.org/10.1038/s12276-018-0144-8 |
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author | Yoon, Ye Ran Lee, Tae-Gul Choi, Mi-Hyun Shin, Seung Woo Ko, Young-Gyu Rhyu, Im Joo Kim, Dong-Hoon Seong, Je Kyung Baik, Ja-Hyun |
author_facet | Yoon, Ye Ran Lee, Tae-Gul Choi, Mi-Hyun Shin, Seung Woo Ko, Young-Gyu Rhyu, Im Joo Kim, Dong-Hoon Seong, Je Kyung Baik, Ja-Hyun |
author_sort | Yoon, Ye Ran |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6135830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61358302018-09-18 Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor Yoon, Ye Ran Lee, Tae-Gul Choi, Mi-Hyun Shin, Seung Woo Ko, Young-Gyu Rhyu, Im Joo Kim, Dong-Hoon Seong, Je Kyung Baik, Ja-Hyun Exp Mol Med Article 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. Nature Publishing Group UK 2018-09-12 /pmc/articles/PMC6135830/ /pubmed/30209265 http://dx.doi.org/10.1038/s12276-018-0144-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yoon, Ye Ran Lee, Tae-Gul Choi, Mi-Hyun Shin, Seung Woo Ko, Young-Gyu Rhyu, Im Joo Kim, Dong-Hoon Seong, Je Kyung Baik, Ja-Hyun Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor |
title | Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor |
title_full | Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor |
title_fullStr | Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor |
title_full_unstemmed | Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor |
title_short | Glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor |
title_sort | glucose-regulated protein 78 binds to and regulates the melanocortin-4 receptor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135830/ https://www.ncbi.nlm.nih.gov/pubmed/30209265 http://dx.doi.org/10.1038/s12276-018-0144-8 |
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