Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Integrins and cytokines activate nuclear transcription factor-κB in human neutrophils

Item Type:Article
Title:Integrins and cytokines activate nuclear transcription factor-κB in human neutrophils
Creators Name:Kettritz, R. and Choi, M. and Rolle, S. and Wellner, M. and Luft, F.C.
Abstract:Neutrophil adhesion to extracellular matrix is necessary for an effective inflammatory response. Adhesion may accelerate neutrophil activation by affecting intracellular signaling pathways. The nuclear transcription factor {kappa}B (NF-{kappa}B) controls several cellular functions, including inflammation, proliferation, and cell survival. We explored the role of adhesion in NF-{kappa}B activation in human neutrophils. Cells were stimulated with tumor necrosis factor-{alpha} (TNF-{alpha}), granulocyte macrophage-colony-stimulating factor (GM-CSF), interleukin-8 (IL-8), and formyl-methionyl-leucyl-phenylalanine (fMLP). All four initiated neutrophil adherence to and spreading on fibronectin. GM-CSF and IL-8 did not activate NF-{kappa}B in suspended neutrophils but rapidly activated NF-{kappa}B under adherent conditions on matrix, as shown by I{kappa}B kinase activity assay, I{kappa}B{alpha} degradation, electromobility shift assay, and quantitative reverse transcriptase-PCR. In contrast, TNF-{alpha} activated NF-{kappa}B both in suspended cells and adherent cells. fMLP did not activate NF-{kappa}B in either suspended or adherent cells. Specific {beta} 2 integrin blockade prevented NF-{kappa}B activation by GM-CSF and IL-8 on fibronectin. Co-stimulating CD18 and CD11b with activating antibodies resulted in NF-{kappa}B activation by GM-CSF and IL-8 in suspended cells. We inhibited actin polymerization with cytochalasin and blocked the non-receptor kinase Syk with piceatannol. Both maneuvers prevented the co-stimulatory NF-{kappa}B-activating signal by {beta} 2 integrins. Thus, in addition to {beta} 2 integrin ligand binding, NF-{kappa}B activation depended on the formation of the receptor-associated intracellular focal adhesion complex. We conclude that {beta} 2 integrins may provide co-stimulatory signals allowing some soluble mediators to activate the NF-{kappa}B pathway even when they are not capable of doing so in suspension. This effect may become important when human neutrophils leave the circulating blood and migrate through extracellular matrix during inflammation.
Keywords:Cytokines, Integrins, Neutrophil Activation, Neutrophil Infiltration, Neutrophils, NF-kappa B, Up-Regulation
Source:Journal of Biological Chemistry
ISSN:0021-9258
Publisher:American Society for Biochemistry and Molecular Biology (U.S.A.)
Volume:279
Number:4
Page Range:2657-2665
Date:23 January 2004
Official Publication:https://doi.org/10.1074/jbc.M309778200
PubMed:View item in PubMed

Repository Staff Only: item control page

Open Access
MDC Library