The neuropeptide neuromedin U promotes IL-6 production from macrophages and endotoxin shock

被引:50
作者
Moriyama, M
Matsukawa, A
Kudoh, S
Takahashi, T
Sato, T
Kano, T
Yoshimura, A
Kojima, M
机构
[1] Kurume Univ, Dept Mol Genet, Inst Life Sci, Kurume, Fukuoka 830, Japan
[2] Kurume Univ, Sch Med, Dept Anesthesiol, Fukuoka, Japan
[3] Kumamoto Univ, Sch Med, Dept Pathol & Expt Med, Grad Sch Med Sci, Kumamoto 860, Japan
[4] Okayama Univ, Dept Pathol & Expt Med, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[5] Kyushu Univ, Med Inst Bioregulat, Div Mol & Cellular Immunol, Higashi Ku, Fukuoka 812, Japan
关键词
neuromedin U; cecal ligation puncture; lipopolysaccharide; IL-6; macrophages;
D O I
10.1016/j.bbrc.2006.01.075
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-alpha 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-RI expression, however, no down-regulation of NMU-RI 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. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1149 / 1154
页数:6
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