Neuropeptides B/W receptor 1
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{{Short description|Protein-coding gene in the species Homo sapiens}}
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Neuropeptides B/W receptor 1, also known as NPBW1 and GPR7, is a human protein encoded by the NPBWR1 gene.{{cite web | title = Entrez Gene: NPBWR1 neuropeptides B/W receptor 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2831}} As implied by its name, it and related gene NPBW2 (with which it shares 70% nucleotide identity) are transmembranes protein that bind Neuropeptide B (NPB) and Neuropeptide W (NPW), both proteins expressed strongly in parts of the brain that regulate stress and fear including the extended amygdala and stria terminalis. When originally discovered in 1995, these receptors had no known ligands ("orphan receptors") and were called GPR7 and GPR8,O’Dowd B. F., Scheideler M. A., Nguyen T., Cheng R., Rasmussen J. S., Marchese A., et al. (1995). The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes, GPR7 and GPR8, expressed in discrete areas of the brain. Genomics 28, 84–91. doi:10.1006/geno.1995.1109 but at least three groups in the early 2000s independently identified their endogenous ligands, triggering the name change in 2005.Davenport A., Singh G. (2005). Neuropeptide W/Neuropeptide B Receptors – NPBW1. IUPHAR Receptor database. doi:10.1786/080844542445
Structure
NPBW1 has seven transmembrane domains, which it unsurprisingly shares with NPBWR2, but also a family of somatostatin and opioid receptors,Hondo M., Ishii M., Sakurai T. (2008). The NPB/NPW neuropeptide system and its role in regulating energy homeostasis, pain, and emotion. Results Probl. Cell Differ. 46, 239–256. doi:10.1007/400_2007_056 and like these proteins couple to Gi-class G proteins.Tanaka H., Yoshida T., Miyamoto N., Motoike T., Kurosu H., Shibata K., et al. (2003). Characterization of a family of endogenous neuropeptide ligands for the G protein-coupled receptors GPR7 and GPR8. Proc. Natl. Acad. Sci. U.S.A. 100, 6251–6256. doi:10.1073/pnas.2233339100
Functions
In rodent models, NPBWR1 is over-expressed in Schwann cells associated with neuropathic pain, suggesting it inhibits inflammatory pain responses.Zaratin P., Quattrini A., Previtali S., Comi G., Hervieu G., Scheideler M. (2005). Schwann cell overexpression of the GPR7 receptor in inflammatory and painful neuropathies. Mol. Cell. Neurosci. 28, 55–63 doi:10.1016/j.mcn.2004.08.010 Mice without NPBW1 exhibited a stronger hostile reaction to intruders, suggesting NPBW1 has a role in stress responses.Nagata-Kuroiwa R., Furutani N., Hara J., Hondo M., Ishii M., Abe T., et al. (2011). Critical role of neuropeptides B/W receptor 1 signaling in social behavior and fear memory. PLoS ONE 6:e16972. doi:10.1371/journal.pone.0016972 Early studies indicated that NPB and NPW had a complex effect on appetite, but generally led to anorexia.Tanaka H., Yoshida T., Miyamoto N., Motoike T., Kurosu H., Shibata K., et al. (2003). Characterization of a family of endogenous neuropeptide ligands for the G protein-coupled receptors GPR7 and GPR8. Proc. Natl. Acad. Sci. U.S.A. 100, 6251–6256. doi:10.1073/pnas.2233339100 Similarly, male rats lacking NPBWR1 exhibited hyperphagia and adult-onset obesity, though why female rats are unaffected is unknown.Ishii M., Fei H., Friedman J. M. (2003). Targeted disruption of GPR7, the endogenous receptor for neuropeptides B and W, leads to metabolic defects and adult-onset obesity. Proc. Natl. Acad. Sci. U.S.A. 100, 10540–10545, doi:10.1073/pnas.1334189100 Researchers speculated that activating these pathways might decrease obesity, and synthesized a small-molecule ligand that is capable of stimulating both receptors at low concentrations.Romero F. A., Hastings N. B., Moningka R., Guo Z., Wang M., Di Salvo J., et al. (2012). The discovery of potent antagonists of NPBWR1 (GPR7). Bioorg. Med. Chem. Lett. 22, 1014–1018. doi:10.1016/j.bmcl.2011.11.126
References
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Further reading
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- {{cite journal |vauthors=O'Dowd BF, Scheideler MA, Nguyen T, etal |title=The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes, GPR7 and GPR8, expressed in discrete areas of the brain |journal=Genomics |volume=28 |issue= 1 |pages= 84–91 |year= 1995 |pmid= 7590751 |doi=10.1006/geno.1995.1109 }}
- {{cite journal |vauthors=Fujii R, Yoshida H, Fukusumi S, etal |title=Identification of a neuropeptide modified with bromine as an endogenous ligand for GPR7 |journal=J. Biol. Chem. |volume=277 |issue= 37 |pages= 34010–6 |year= 2002 |pmid= 12118011 |doi= 10.1074/jbc.M205883200 |doi-access= free }}
- {{cite journal |vauthors=Shimomura Y, Harada M, Goto M, etal |title=Identification of neuropeptide W as the endogenous ligand for orphan G-protein-coupled receptors GPR7 and GPR8 |journal=J. Biol. Chem. |volume=277 |issue= 39 |pages= 35826–32 |year= 2002 |pmid= 12130646 |doi= 10.1074/jbc.M205337200 |doi-access= free }}
- {{cite journal |vauthors=Brezillon S, Lannoy V, Franssen JD, etal |title=Identification of natural ligands for the orphan G protein-coupled receptors GPR7 and GPR8 |journal=J. Biol. Chem. |volume=278 |issue= 2 |pages= 776–83 |year= 2003 |pmid= 12401809 |doi= 10.1074/jbc.M206396200 |doi-access= free }}
- {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |bibcode=2002PNAS...9916899M |doi-access=free }}
- {{cite journal |vauthors=Tanaka H, Yoshida T, Miyamoto N, etal |title=Characterization of a family of endogenous neuropeptide ligands for the G protein-coupled receptors GPR7 and GPR8 |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=100 |issue= 10 |pages= 6251–6 |year= 2003 |pmid= 12719537 |doi= 10.1073/pnas.0837789100 | pmc=156358 |bibcode=2003PNAS..100.6251T |doi-access=free }}
- {{cite journal |vauthors=Zaratin PF, Quattrini A, Previtali SC, etal |title=Schwann cell overexpression of the GPR7 receptor in inflammatory and painful neuropathies |journal=Mol. Cell. Neurosci. |volume=28 |issue= 1 |pages= 55–63 |year= 2005 |pmid= 15607941 |doi= 10.1016/j.mcn.2004.08.010 |s2cid=40483027 }}
- {{cite journal |vauthors=Mazzocchi G, Rebuffat P, Ziolkowska A, etal |title=G protein receptors 7 and 8 are expressed in human adrenocortical cells, and their endogenous ligands neuropeptides B and w enhance cortisol secretion by activating adenylate cyclase- and phospholipase C-dependent signaling cascades |journal=J. Clin. Endocrinol. Metab. |volume=90 |issue= 6 |pages= 3466–71 |year= 2005 |pmid= 15797961 |doi= 10.1210/jc.2004-2132 |doi-access= free }}
- {{cite journal |vauthors=Cottrell S, Jung K, Kristiansen G, etal |title=Discovery and validation of 3 novel DNA methylation markers of prostate cancer prognosis |journal=J. Urol. |volume=177 |issue= 5 |pages= 1753–8 |year= 2007 |pmid= 17437806 |doi= 10.1016/j.juro.2007.01.010 }}
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External links
- {{cite web | url = http://www.iuphar-db.org/GPCR/ReceptorDisplayForward?receptorID=3002 | title = Neuropeptide B/W Receptors: NPBW1 | work = IUPHAR Database of Receptors and Ion Channels | publisher = International Union of Basic and Clinical Pharmacology }}
{{G protein-coupled receptors}}
{{DEFAULTSORT:Neuropeptides B W receptor 1}}