Differential regulation of indoleamine 2,3-dioxygenase by lipopolysaccharide and interferon gamma in murine bone marrow derived dendritic cells

被引:73
作者
Jung, In Duk
Lee, Chang-Min
Jeong, Young-Il
Lee, Jun Sik
Park, Won Sun
Han, Jin
Park, Yeong-Min
机构
[1] Pusan Natl Univ, Med Res Inst, Dept Microbiol & Immunol, Pusan 602739, South Korea
[2] Pusan Natl Univ, Natl Res Lab Dendrit Cell Differentiat & Regulat, Med Res Inst, Pusan 602739, South Korea
[3] Pusan Natl Univ, Coll Nat Sci, Dept Microbiol, Pusan 609735, South Korea
[4] Pusan Natl Univ, Coll Pharm, Dept Pharm, Pusan 609735, South Korea
[5] Inje Univ, Coll Med, Dept Physiol & Biophys, FIRST Project Grp,Mitochondria Signaling Lab, Pusan 614735, South Korea
来源
FEBS LETTERS | 2007年 / 581卷 / 07期
关键词
indoleamine 2,3-dioxygenase; dendritic cells; lipopolysaccharide;
D O I
10.1016/j.febslet.2007.02.073
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
Indoleamine 2,3-dioxygenase (IDO) is a rate-limiting enzyme in the L-tryptophan-kynurenine pathway, which converts an essential amino acid, L-tryptophan, to N-formylkynurenine. The expression of IDO increases when inflammation is induced by wounding, infection or tumor growth. Although recent studies have suggested that IDO expression is up-regulated by IFN-gamma in various cell types and that the induction of IDO can also be mediated through an IFN-gamma-independent mechanism, these mechanisms still remain unknown. In this study, we investigated whether lipopolysaccharide (LPS) induces the expression of IDO through an IFN-gamma-mediated signaling pathway or not. IFN-gamma-induced expression of IDO expression was inhibited only by JAK inhibitor I. However, LPS-induced expression of IDO was inhibited by LY294002 and SP600125 but not by JAK inhibitor 1, SB203580, or U0126. These findings clearly indicate that LPS can induce the IDO expression via an IFN-gamma-independent mechanism and PI3 kinase and JNK in the LPS-induced pathway leading to IDO expression. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1449 / 1456
页数:8
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