Endotoxin Down‐Regulates Monocyte and Granulocyte Interleukin‐6 Receptors without Influencing gp130 Expression in Humans
Author(s) -
Pascale E. P. Dekkers,
Nicole P. Juffermans,
Tessa ten Hove,
Evert de Jonge,
Sander J. H. van Deventer,
Tom van der Poll
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315356
Subject(s) - lipopolysaccharide , monocyte , proinflammatory cytokine , receptor , granulocyte , glycoprotein 130 , receptor expression , immunology , interleukin 19 , interleukin , biology , cytokine , interleukin 6 receptor , inflammation , interleukin 6 , chemistry , biochemistry , interleukin 5
Interleukin (IL)-6 is important for host defense against various pathogens. The IL-6 receptor (IL-6R) complex consists of a ligand-binding component (IL-6R) and a signal-transducing component (gp130). In a study designed to obtain insight into the regulation of this receptor complex during inflammation, 8 healthy subjects received an intravenous injection of lipopolysaccharide (LPS; 4 ng/kg), and receptor expression was determined on blood leukocytes by use of fluorescence-activated cell cytometry. LPS induced a transient decrease in monocyte and granulocyte IL-6R expression but did not influence gp130. The plasma concentrations of soluble IL-6R and soluble gp130 did not change after LPS administration. Expression of the receptor for leukemia inhibitory factor, a member of the IL-6R family, remained unaltered after LPS injection. In whole blood in vitro, LPS and gram-positive stimuli and proinflammatory cytokines were capable of down-modulating the IL-6R. Monocytes and granulocytes may down-regulate IL-6R at their surface upon their first interaction with bacterial antigens.
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