Chemoattractants induce a rapid and transient upregulation of monocyte α4 integrin affinity for vascular cell adhesion molecule 1 which mediates arrest:: An early step in the process of emigration
被引:118
作者:
Chan, JR
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机构:Toronto Gen Res Inst, Toronto, ON M5G 2C4, Canada
Chan, JR
Hyduk, SJ
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机构:Toronto Gen Res Inst, Toronto, ON M5G 2C4, Canada
Hyduk, SJ
Cybulsky, MI
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机构:Toronto Gen Res Inst, Toronto, ON M5G 2C4, Canada
Cybulsky, MI
机构:
[1] Toronto Gen Res Inst, Toronto, ON M5G 2C4, Canada
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 2C4, Canada
stromal cell-derived factor 1 alpha;
chemokines;
formyl peptide;
very late antigen 4;
inflammation;
D O I:
10.1084/jem.193.10.1149
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Chemoattractants and chemokines induce arrest of rolling monocytes during emigration from blood into tissues. In this study, we demonstrated that alpha4 integrin affinity for vascular cell adhesion molecule (VCAM)-1 was upregulated rapidly and transiently by chemoattractants and stromal cell-derived factor (SDF)-1 alpha and mediated monocyte arrest. alpha4 integrin affinity changes were detected and blocked using soluble VCAM-1/Fc (sVCAM-1/Fc). In a now cytometry assay, markedly increased sVCAM-1/Fc binding to human blood monocytes or U937 cells transfected with formyl peptide (FP) receptor was detected 30 s after FP or SDF-1 alpha treatment and declined after 2 min. In a parallel plate flow chamber assay, FP, C5a, platelet-activating factor, or SDF-1 alpha coimmobilized with VCAM-1 induced leukocyte arrest, which was blocked by inclusion of sVCAM-1/Fc but not soluble nonimmune immunoglobulin G in the assay buffer.