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Adherence influences monocyte responsiveness to interleukin-10
Anne-France Petit-Bertron1, Catherine Fitting, Jean-Marc Cavaillon
1UP Cytokines & Inflammation, Institut Pasteur, 28 rue Dr Roux, 75015 Paris, France.
Journal of Leukocyte Biology
|January 15, 2003
Summary
Cell adherence significantly impacts interleukin-10 (IL-10) effects on monocytes. Adherence enhances IL-10
Area of Science:
- Immunology
- Cell Biology
Background:
- Interleukin-10 (IL-10) is a key anti-inflammatory cytokine.
- Monocyte function is influenced by their adherence properties.
Purpose of the Study:
- To investigate how monocyte adherence affects IL-10's biological properties.
- To elucidate the role of adherence in modulating IL-10-mediated anti-inflammatory responses.
Main Methods:
- Monocyte-enriched peripheral blood mononuclear cells were cultured under adherent and non-adherent conditions.
- Cells were treated with IL-10, and effects on CD11b expression, Toll-like receptor (TLR) expression and function, cytokine production, phagocytosis, and signaling pathways (STAT3, Tyk2, SOCS3) were assessed.
- Heme oxygenase-1 expression was analyzed.
Main Results:
- Adherence enhanced IL-10-induced decrease in CD11b expression.
- IL-10 upregulated TLR2 and TLR4 mRNA and TLR4 surface expression in adherent cells.
- Absence of adherence abrogated IL-10's inhibitory effects on lipopolysaccharide-induced TNF and G-CSF production, and increased IL-1beta and soluble TNF receptor II release.
- Adherence amplified IL-10's enhancement of phagocytosis.
- IL-10 induced STAT3/Tyk2 phosphorylation and SOCS3 expression, with prolonged activation in adherent monocytes.
- Heme oxygenase-1 was induced by IL-10 in adherent monocytes but not in non-adherent cells.
Conclusions:
- Monocyte adherence significantly modulates the anti-inflammatory properties and functional outcomes of IL-10.
- Adherence enhances IL-10's effects on immune cell function, including receptor expression, cytokine regulation, and phagocytosis.
- These findings highlight the importance of cellular context in understanding cytokine signaling and immune responses.