Jung In Duk, Lee Chang-Min, Jeong Young-Il, Lee Jun Sik, Park Won Sun, Han Jin, Park Yeong-Min
Department of Microbiology and Immunology and National Research Laboratory of Dendritic, Cell Differentiation and Regulation, Medical Research Institute, Pusan National University, College of Medicine, Ami-dong 1-10, Seo-gu, Busan 602-739, South Korea.
FEBS Lett. 2007 Apr 3;581(7):1449-56. doi: 10.1016/j.febslet.2007.02.073. Epub 2007 Mar 7.
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 I, 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.
吲哚胺2,3-双加氧酶(IDO)是L-色氨酸-犬尿氨酸途径中的一种限速酶,它将必需氨基酸L-色氨酸转化为N-甲酰犬尿氨酸。当因创伤、感染或肿瘤生长引发炎症时,IDO的表达会增加。尽管最近的研究表明,在各种细胞类型中IFN-γ可上调IDO的表达,且IDO的诱导也可通过不依赖IFN-γ的机制介导,但这些机制仍不清楚。在本研究中,我们调查了脂多糖(LPS)是否通过IFN-γ介导的信号通路诱导IDO的表达。仅JAK抑制剂I抑制了IFN-γ诱导的IDO表达。然而,LY294002和SP600125抑制了LPS诱导的IDO表达,而JAK抑制剂I、SB203580或U0126则没有。这些发现清楚地表明,LPS可通过不依赖IFN-γ的机制以及LPS诱导IDO表达途径中的PI3激酶和JNK诱导IDO表达。
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