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Influence of interleukin-4 and platelet-activating factor on the Fc epsilon RII/CD23 expression on human monocytes
N Paul-Eugène1, B Dugas, S Picquot
1Institut Henri Beaufour, Les Ulis, France.
Insights
Platelet-activating factor (PAF) increases the expression of the IgE receptor (Fc epsilon RII/CD23) on monocytes. This finding suggests a potential role for PAF in allergic diseases.
Area of Science:
- Immunology
- Cell Biology
- Allergy Research
Background:
- The low-affinity receptor for IgE (Fc epsilon RII/CD23) plays a role in allergic responses.
- Interleukin-4 (IL-4) is known to induce Fc epsilon RII/CD23 expression on monocytes.
Purpose of the Study:
- To investigate the effect of platelet-activating factor (PAF) on Fc epsilon RII/CD23 expression in human monocytes.
- To compare the effects of PAF and IL-4 on Fc epsilon RII/CD23 expression.
Main Methods:
- Human monocytes were treated with recombinant IL-4 or PAF.
- Fc epsilon RII/CD23 expression was assessed using flow cytometry.
- The effects of PAF antagonists (BN 52021, BN 50730) and anti-IL-4 antiserum were evaluated.
Main Results:
- Both IL-4 and PAF induced Fc epsilon RII/CD23 expression on human monocytes.
- PAF-induced expression was time- and dose-dependent, with maximal effects at 1 microM PAF after 24 hours.
- PAF-induced expression was inhibited by PAF antagonists, but not by anti-IL-4 antiserum.
- IL-4-induced expression was abolished by anti-IL-4 antiserum and slightly reduced by PAF antagonists.
Conclusions:
- PAF significantly regulates Fc epsilon RII/CD23 expression on human monocytes.
- These findings suggest a novel role for PAF in the context of allergic diseases.
Abstract:
Human recombinant interleukin-4 (IL-4) induces the expression of the low-affinity receptor for IgE (Fc epsilon RII/CD23) on human normal monocytes as assessed by flow cytometry. Also, platelet-activating factor (PAF) induces a time- and dose-dependent increase in Fc epsilon RII/CD23 expression, which is maximal with 1 microM PAF and after a 24-h incubation period. Under similar experimental conditions, lyso-PAF (1 microM) has no effect on Fc epsilon RII/CD23 expression. The PAF-induced Fc epsilon RII/CD23 expression on human monocytes is inhibited by two unrelated antagonists of the mediator, namely BN 52021 and BN 50730, but is not significantly affected when the cells are incubated in the presence of a rabbit anti-IL-4 antiserum. The IL-4-induced Fc epsilon RII/CD23 is abolished in the presence of the anti-IL-4 antiserum and slightly (not significantly) reduced when BN 52021 or BN 50730 is added to the incubation medium. These results suggest that PAF regulates Fc epsilon RII/CD23 expression and may indicate a new role for this autacoid in allergic diseases.
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