Oncostatin M is a proinflammatory mediator - In vivo effects correlate with endothelial cell expression of inflammatory cytokines and adhesion molecules

被引:174
作者
Modur, V
Feldhaus, MJ
Weyrich, AS
Jicha, DL
Prescott, SM
Zimmerman, GA
McIntyre, TM
机构
[1] UNIV UTAH,NORA ECCLES HARRISON CVRTI,SCH MED,SALT LAKE CITY,UT 84112
[2] UNIV UTAH,DEPT PATHOL,SCH MED,SALT LAKE CITY,UT 84112
[3] UNIV UTAH,SCH MED,DEPT INTERNAL MED,DIV VASC SURG,SALT LAKE CITY,UT 84112
[4] UNIV UTAH,SCH MED,PROGRAM HUMAN MOL BIOL & GENET,SALT LAKE CITY,UT 84112
关键词
neutrophils; E-selectin; P-selectin; IL-6; IL-8;
D O I
10.1172/JCI119508
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Oncostatin M is a member of the IL-6 family of cytokines that is primarily known for its effects on cell growth. Endothelial cells have an abundance of receptors for oncostatin hi, and may be its primary target. We determined if oncostatin M induces a key endothelial cell function, initiation of the inflammatory response, We found that subcutaneous injection of oncostatin RI in mice caused an acute inflammatory reaction, Oncostatin M in vitro stimulated: (a) polymorphonuclear leukocyte (PMN) transmigration through confluent monolayers of primary human endothelial cells; (b) biphasic PMN adhesion through rapid P-selectin expression, and delayed adhesion mediated by E-selectin synthesis; (c) intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 accumulation: and (d) the expression of PMN activators IL-6, epithelial neutrophil activating peptide-78, growth-related cytokine alpha and growth-related cytokine beta without concomitant IL-g synthesis, The nature of the response to oncostatin M varied with concentration, suggesting high and low affinity oncostatin M receptors independently stimulated specific responses, Immunohistochemistry showed that macrophage-like cells infiltrating human aortic aneurysms expressed oncostatin RI, so it is present during a chronic inflammatory reaction, Therefore, oncostatin M, but not other IL-6 family members, fulfills Koch's postulates as an inflammatory mediator, Since its effects on endothelial cells differ significantly from established mediators like TNF alpha. it ma uniquely contribute to the inflammatory cycle.
引用
收藏
页码:158 / 168
页数:11
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