The calcium-binding protein S100A12 induces neutrophil adhesion, migration, and release from bone marrow in mouse at concentrations similar to those found in human inflammatory arthritis

被引:77
作者
Rouleau, P
Vandal, K
Ryckman, C
Poubelle, PE
Boivin, A
Talbot, M
Tessier, PA
机构
[1] CHU Laval, Infect Dis Res Ctr, Ste Foy, PQ G1V 4G2, Canada
[2] CHU Laval, Rheumatol & Immunol Res Ctr, Ste Foy, PQ G1V 4G2, Canada
关键词
neutrophils; inflammation; rheumatoid arthritis; chemotaxis; cell trafficking; calcium-binding proteins; T-CELL CHEMOATTRACTANT; INNATE HOST DEFENSES; LEUKOCYTE L1 PROTEIN; ANTIMICROBIAL PEPTIDES; CALPROTECTIN; CHEMOKINES; IDENTIFICATION; MECHANISM; CYTOKINES; RECEPTOR;
D O I
10.1016/S1521-6616(02)00043-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated the proinflammatory activities of S100A12 in the context of synovial inflammation. S100A12 levels were increased in the synovial fluids and plasma of patients with gout, rheumatoid arthritis, psoriatic arthritis, and undetectable in osteoarthritis, a noninflammatory disorder. S100A12 proved to induce neutrophil adhesion to fibrinogen via Mac-1 at concentrations similar to those found in the synovial fluids. Similar concentrations induced the recruitment of large numbers of neutrophils and monocytes in the murine air pouch model. To characterize the effect of increased S100A12 plasma levels, mice were injected intravenously with S100A12. This led to the mobilization of neutrophils from the bone marrow to the peripheral blood. These results suggest that S100A12 stimulates the accumulation of neutrophil by inducing their release from the bone marrow, as well as by activating their adhesion and migration toward inflammatory sites. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:46 / 54
页数:9
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