TY - JOUR
T1 - The neuropeptide neuromedin U promotes IL-6 production from macrophages and endotoxin shock
AU - Moriyama, Maiko
AU - Matsukawa, Akihiro
AU - Kudoh, Shinji
AU - Takahashi, Tomoko
AU - Sato, Takahiro
AU - Kano, Tatsuhiko
AU - Yoshimura, Akihiko
AU - Kojima, Masayasu
N1 - Funding Information:
This work was supported by the Program for Promotion of Basic Research Activities for Innovative Biosciences (PROBRAIN), the Mochida Memorial Foundation, and Grants-in-Aid for Scientific Research (B) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (to M.K.), and the MEXT Open Research Center Project (2004).
PY - 2006/3/24
Y1 - 2006/3/24
N2 - Neuromedin U (NMU) is a neuropeptide involved in appetite, circadian rhythm, and pronociception. However, the NMU receptor NMU-R1 has been shown to be expressed in immune cells and NMU promotes mast cell-dependent inflammation. In this study, we demonstrated that NMU plays an important role in IL-6 production in macrophages. NMU-deficient mice were resistant against cecal ligation puncture- as well as LPS-induced septic shock. IL-6 but not TNF-α levels were markedly reduced in LPS-treated NMU-deficient mice compared with wild type mice. Both NMU and NMU-R1 were expressed in wild type peritoneal macrophages, and treatment with LPS resulted in up-regulation of NMU but down-regulation of NMU-R1 expression, however, no down-regulation of NMU-R1 was observed in NMU-deficient macrophages where LPS-induced IL-6 production was severely reduced. These data suggest that LPS-induced IL-6 expression is partly dependent on autocrine/paracrine activation of the NMU-NMU-R1 signals in macrophages.
AB - Neuromedin U (NMU) is a neuropeptide involved in appetite, circadian rhythm, and pronociception. However, the NMU receptor NMU-R1 has been shown to be expressed in immune cells and NMU promotes mast cell-dependent inflammation. In this study, we demonstrated that NMU plays an important role in IL-6 production in macrophages. NMU-deficient mice were resistant against cecal ligation puncture- as well as LPS-induced septic shock. IL-6 but not TNF-α levels were markedly reduced in LPS-treated NMU-deficient mice compared with wild type mice. Both NMU and NMU-R1 were expressed in wild type peritoneal macrophages, and treatment with LPS resulted in up-regulation of NMU but down-regulation of NMU-R1 expression, however, no down-regulation of NMU-R1 was observed in NMU-deficient macrophages where LPS-induced IL-6 production was severely reduced. These data suggest that LPS-induced IL-6 expression is partly dependent on autocrine/paracrine activation of the NMU-NMU-R1 signals in macrophages.
KW - Cecal ligation puncture
KW - IL-6
KW - Lipopolysaccharide
KW - Macrophages
KW - Neuromedin U
UR - http://www.scopus.com/inward/record.url?scp=32344438877&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=32344438877&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2006.01.075
DO - 10.1016/j.bbrc.2006.01.075
M3 - Article
C2 - 16466693
AN - SCOPUS:32344438877
SN - 0006-291X
VL - 341
SP - 1149
EP - 1154
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -