Up-regulation of IL-18BP, but not IL-18 mRNA in rat liver by LPS

被引:8
作者
Wheeler, RD
Young, EA
Rothwell, NJ
Hall, MD
Luheshi, GN
机构
[1] Univ Manchester, Sch Biol Sci, Manchester M13 9PT, Lancs, England
[2] AstraZeneca R&D Charnwood, Discovery, Loughborough LE11 5RH, Leics, England
[3] GlasoSmithKline Pharmaceut, Harlow CM19 5AW, Essex, England
[4] McGill Univ, Douglas Hosp, Res Ctr, Verdun, PQ H4H 1R3, Canada
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
IL-18BP; interleukin 18 binding protein;
D O I
10.1016/S1043-4666(03)00028-0
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
Interleukin (IL)-18 is a pro-inflammatory cytokine that plays a critical role in inflammation leading to liver damage, through promotion of Fas-mediated apoptosis. Inhibition of IL-18 activity protects against LPS-induced lethality in mice and against liver damage induced by LPS after sensitisation of mice with Proprionibacterium acnes. A specific, potent, endogenous inhibitor of IL-18 (IL-18BP) has been identified in mice and humans, and IL-18BP mRNA is expressed constitutively in liver. The objectives of this study were to compare changes in IL-1beta and IL-18 mRNA expression in the liver of rats in response to peripheral injection of LPS, using real-time PCR, and also to investigate whether IL-18BP mRNA expression is affected by this treatment. LPS rapidly up-regulated IL-1beta mRNA expression, but IL-18 mRNA expression was unaffected by LPS treatment. Unlike IL-18, IL-18BP mRNA was up-regulated dramatically by approximately 12-fold above naive levels, peaking 3 h after LPS injection. This ability of LPS to up-regulate expression of the endogenous IL-18 inhibitor may indicate a mechanism by which the inflammatory response to LPS is regulated. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:161 / 166
页数:6
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