Myeloid-related proteins 8 and 14 induce a specific inflammatory response in human microvascular endothelial cells

被引:265
作者
Viemann, D
Strey, A
Janning, A
Jurk, K
Klimmek, K
Vogl, T
Hirono, K
Ichida, F
Foell, D
Kehrel, B
Gerke, V
Sorg, C
Roth, J
机构
[1] Univ Hosp Muenster, Inst Expt Dermatol, Dept Pediat, D-48149 Munster, Germany
[2] Univ Hosp Muenster, Inst Expt Dermatol, Dept Anaesthesia & Intens Care, D-48149 Munster, Germany
[3] Univ Munster, Inst Expt Dermatol, D-4400 Munster, Germany
[4] Univ Munster, Inst Med Biochem, Ctr Mol Biol & Inflammat, D-4400 Munster, Germany
[5] Univ Munster, Interdisciplinary Clin Res Ctr, D-4400 Munster, Germany
[6] Toyama Med & Pharmaceut Univ, Dept Pediat, Toyama, Japan
关键词
D O I
10.1182/blood-2004-07-2520
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myeloid-related protein 8 (MRP8) and MRP14, S100 proteins secreted by activated phagocytes, bind specifically to endothelial cells. The endothelial response to MRP8/MRP14, however, is unknown. Using oligonucleotide microarray analysis, we show for the first time that MRP8/MRP14 induce a thrombogenic, inflammatory response in human microvascular endothelial cells by increasing thetranscription of proinflammatory chemokines and adhesion molecules and by decreasing the expression of cell junction proteins and molecules involved in monolayer integrity. All changes on the gene expression level could be confirmed using biochemical and functional assays. We demonstrated that the expression of MRP8/MRP14 closely correlated with the inflammatory activity in systemic vasculitis, confirming the important role of these proteins for distinct inflammatory reactions in endothelia. MRP8/MRP14 may represent novel targets for anti-inflammatory strategies.
引用
收藏
页码:2955 / 2962
页数:8
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