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The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells
Neuromedin U (NMU) is a neuropeptide that is expressed in the gastrointestinal tract and central nervous system. NMU interacts with two G protein–coupled receptors, NMU-R1 and NMU-R2. Whereas NMU-R2 localizes predominantly to nerve cells, NMU-R1 is expressed in peripheral tissues including lymphocyt...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213011/ https://www.ncbi.nlm.nih.gov/pubmed/16009716 http://dx.doi.org/10.1084/jem.20050248 |
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author | Moriyama, Maiko Sato, Takahiro Inoue, Hiromasa Fukuyama, Satoru Teranishi, Hitoshi Kangawa, Kenji Kano, Tatsuhiko Yoshimura, Akihiko Kojima, Masayasu |
author_facet | Moriyama, Maiko Sato, Takahiro Inoue, Hiromasa Fukuyama, Satoru Teranishi, Hitoshi Kangawa, Kenji Kano, Tatsuhiko Yoshimura, Akihiko Kojima, Masayasu |
author_sort | Moriyama, Maiko |
collection | PubMed |
description | Neuromedin U (NMU) is a neuropeptide that is expressed in the gastrointestinal tract and central nervous system. NMU interacts with two G protein–coupled receptors, NMU-R1 and NMU-R2. Whereas NMU-R2 localizes predominantly to nerve cells, NMU-R1 is expressed in peripheral tissues including lymphocytes and monocytes, suggesting a role of NMU in immunoregulation. However, the functions of NMU in peripheral tissues have not been clarified. In this study, using NMU-deficient mice, we first demonstrated that NMU plays an important role in mast cell-mediated inflammation. Complete Freund's adjuvant-induced mast cell degranulation as well as edema and neutrophil infiltration, which occurred weakly in mast cell–deficient WBB6F(1)-W/W (v) mice, did not occur in NMU-deficient mice. Moreover, intraplantar injection of NMU into paws induced early inflammatory responses such as mast cell degranulation, vasodilation, and plasma extravasation in WT mice but not in WBB6F(1)-W/W (v) mice. NMU-R1 was highly expressed in primary mast cells, and NMU induced Ca(2+) mobilization and degranulation in peritoneal mast cells. These data indicate that NMU promotes mast cell–mediated inflammation; therefore, NMU receptor antagonists could be a novel target for pharmacological inhibition of mast cell–mediated inflammatory diseases. |
format | Text |
id | pubmed-2213011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22130112008-03-11 The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells Moriyama, Maiko Sato, Takahiro Inoue, Hiromasa Fukuyama, Satoru Teranishi, Hitoshi Kangawa, Kenji Kano, Tatsuhiko Yoshimura, Akihiko Kojima, Masayasu J Exp Med Brief Definitive Report Neuromedin U (NMU) is a neuropeptide that is expressed in the gastrointestinal tract and central nervous system. NMU interacts with two G protein–coupled receptors, NMU-R1 and NMU-R2. Whereas NMU-R2 localizes predominantly to nerve cells, NMU-R1 is expressed in peripheral tissues including lymphocytes and monocytes, suggesting a role of NMU in immunoregulation. However, the functions of NMU in peripheral tissues have not been clarified. In this study, using NMU-deficient mice, we first demonstrated that NMU plays an important role in mast cell-mediated inflammation. Complete Freund's adjuvant-induced mast cell degranulation as well as edema and neutrophil infiltration, which occurred weakly in mast cell–deficient WBB6F(1)-W/W (v) mice, did not occur in NMU-deficient mice. Moreover, intraplantar injection of NMU into paws induced early inflammatory responses such as mast cell degranulation, vasodilation, and plasma extravasation in WT mice but not in WBB6F(1)-W/W (v) mice. NMU-R1 was highly expressed in primary mast cells, and NMU induced Ca(2+) mobilization and degranulation in peritoneal mast cells. These data indicate that NMU promotes mast cell–mediated inflammation; therefore, NMU receptor antagonists could be a novel target for pharmacological inhibition of mast cell–mediated inflammatory diseases. The Rockefeller University Press 2005-07-18 /pmc/articles/PMC2213011/ /pubmed/16009716 http://dx.doi.org/10.1084/jem.20050248 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Brief Definitive Report Moriyama, Maiko Sato, Takahiro Inoue, Hiromasa Fukuyama, Satoru Teranishi, Hitoshi Kangawa, Kenji Kano, Tatsuhiko Yoshimura, Akihiko Kojima, Masayasu The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells |
title | The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells |
title_full | The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells |
title_fullStr | The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells |
title_full_unstemmed | The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells |
title_short | The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells |
title_sort | neuropeptide neuromedin u promotes inflammation by direct activation of mast cells |
topic | Brief Definitive Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213011/ https://www.ncbi.nlm.nih.gov/pubmed/16009716 http://dx.doi.org/10.1084/jem.20050248 |
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