TY - JOUR
T1 - The neuropeptide neuromedin U promotes inflammation by direct activation of mast cells
AU - Moriyama, Maiko
AU - Sato, Takahiro
AU - Inoue, Hiromasa
AU - Fukuyama, Satoru
AU - Teranishi, Hitoshi
AU - Kangawa, Kenji
AU - Kano, Tatsuhiko
AU - Yoshimura, Akihiko
AU - Kojima, Masayasu
PY - 2005/7/18
Y1 - 2005/7/18
N2 - 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/Wv 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 WBB6F1 - W/Wv 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.
AB - 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/Wv 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 WBB6F1 - W/Wv 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.
UR - http://www.scopus.com/inward/record.url?scp=22944465107&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=22944465107&partnerID=8YFLogxK
U2 - 10.1084/jem.20050248
DO - 10.1084/jem.20050248
M3 - Article
C2 - 16009716
AN - SCOPUS:22944465107
SN - 0022-1007
VL - 202
SP - 217
EP - 224
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 2
ER -