A novel cytokine receptor-ligand pair -: Identification, molecular characterization, and in vivo immunomodulatory activity

被引:183
作者
Shi, YG
Ullrich, SJ
Zhang, J
Connolly, K
Grzegorzewski, KJ
Barber, MC
Wang, W
Wathen, K
Hodge, V
Fisher, CL
Olsen, H
Ruben, SM
Knyazev, I
Cho, YH
Kao, V
Wilkinson, KA
Carrell, JA
Ebner, R
机构
[1] Human Genome Sci Inc, Dept Mol Biol, Rockville, MD 20850 USA
[2] Human Genome Sci Inc, Dept Prot Dev, Rockville, MD 20850 USA
[3] Human Genome Sci Inc, Dept Strateg Drug Dev, Rockville, MD 20850 USA
[4] Human Genome Sci Inc, Dept Cell Biol, Rockville, MD 20850 USA
关键词
D O I
10.1074/jbc.M910228199
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
As part of a large scale effort to discover novel secreted proteins, a cDNA encoding a novel cytokine was identified. Alignments of the sequence of the new protein, designated IL-17B, suggest it to be a homolog of the recently described T cell-derived cytokine, IL-17. By Northern analysis, EST distribution and real-time quantitative polymerase chain reaction analysis, mRNA was detected in many cell types. A novel type I transmembrane protein, identified in an EST data base by homology to IL-17R, was found to bind specifically IL-17B, as determined by surface plasmon resonance analysis, flow cytometry, and co-immunoprecipitation experiments. Readily detectable transcription of IL-17BR was restricted to human kidney, pancreas, liver, brain, and intestines and only a few of the many cell lines tested. By using. a rodent ortholog of IL-17BR as a probe, IL-17BR message was found to be drastically up-regulated during intestinal inflammation elicited by indomethacin treatment in rats. In addition, intraperitoneal injection of IL-17B purified from Chinese hamster ovary cells caused marked neutrophil migration in normal mice, in a specific and dose-dependent manner. Together these results suggest that IL-17B may be a novel proinflammatory cytokine acting on a restricted set of target cell types. They also demonstrate the strength of genomic approaches in the unraveling of novel biological pathways.
引用
收藏
页码:19167 / 19176
页数:10
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