Identification of a truncated IL-18β mRNA:: a putative regulator of IL-18 expressed in rat brain

被引:37
作者
Andre, R
Wheeler, RD
Collins, PD
Luheshi, GN
Pickering-Brown, S
Kimber, I
Rothwell, NJ
Pinteaux, E
机构
[1] Univ Manchester, Sch Biol Sci, Manchester M13 9PT, Lancs, England
[2] Montreal Neurol Inst, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Douglas Hosp, Res Ctr, Verdun, PQ H4H 1R3, Canada
[4] Kings Coll London, Inst Psychiat, Old Age Psychiat Sect, London SE5 8AF, England
[5] Syngenta Cent Toxicol Lab, Macclesfield SK10 4TJ, Cheshire, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
interleukins; IL-18; cytokine receptors; EAE;
D O I
10.1016/j.jneuroim.2003.09.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin (IL)-18, a member of the IL-1 family, is a key mediator of peripheral inflammation and host defense responses, and has been implicated in inflammatory and neurodegenerative diseases in the brain. IL-18 acts via a receptor complex that closely resembles that of IL-1, consisting of a ligand binding protein, IL-18Ralpha, and an accessory protein, IL-18Rbeta. Here, we describe the presence of a splice variant of IL-18Rbeta that is predicted to encode a truncated soluble protein, consisting of only the first immunoglobulin-like domain of IL-18Rbeta (EMBL/ Genbank accession number AJ550893). Both forms of IL-18Rbeta were expressed in rat cortex, striatum, hypothalamus, hippocampus, and also liver, and were detected in pure cultures of microglia, astrocytes and neurons. This novel splice variant is up-regulated rapidly in microglial cells by bacterial lipopolyssacharide (LPS). We propose that this putative truncated form of IL-18Rbeta is analogous to the soluble form of IL-1R accessory protein, and could act as an important regulator of IL-18 actions. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:40 / 45
页数:6
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