Premium
Aggregation of β 2 integrins activates human neutrophils through the IκB/NF‐κB pathway
Author(s) -
Kim Cheol Hyeon,
Lee KyoungHee,
Lee ChoonTaek,
Kim Young Whan,
Han Sung Koo,
Shim YoungSoo,
Yoo ChulGyu
Publication year - 2004
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.0103038
Subject(s) - integrin , cd18 , integrin alpha m , biology , microbiology and biotechnology , neutrophil extracellular traps , tumor necrosis factor alpha , immunology , inflammation , receptor , biochemistry , flow cytometry
Neutrophils are now considered central to the pathogenesis of most forms of acute lung injury. Neutrophils do not cause damage while suspended in the bloodstream; however, a release of cytotoxic agents occurs when neutrophils are adherent to endothelium, epithelium, or extracellular matrix proteins in the interstitium. Such neutrophil adherence is mediated predominantly through β 2 integrins (CD11/CD18) on its surface. This study was undertaken to investigate whether the IκB/nuclear factor (NF)‐κB cascade is involved in this β 2 integrin‐mediated activation of human neutrophils. β 2 Integrin Mac‐1 (CD11b/CD18) aggregation was induced by antibody cross‐linking of the integrins on the cell surface. β 2 Integrin aggregation induced interleukin‐1β and tumor necrosis factor‐α production, which suggests the activation of neutrophils by β 2 integrin. IκBα was markedly degraded at 1 h, and NF‐κB–DNA‐binding activity markedly increased 2 h after β 2 integrin aggregation, which activated IκB kinase activity at 1 h. β 2 Integrin‐induced cytokine production was suppressed by MG132 or SN50 pretreatment, which blocked the activation of NF‐κB. These findings suggest that the activation of human neutrophils by β 2 integrin aggregation is mediated through the activation of the IκB/NF‐κB pathway.