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Peripheral Blood CD14high CD16⁺ Monocytes are Main Producers of IL-10

Based on CD14 and CD16 expression, human peripheral blood monocytes (MO) can be divided into a major CD14high CD16⁻ population and two minor CD14high CD16⁺ and CD14dim CD16⁺ subpopulations. CD14dim CD16⁺ MO are well characterized and regarded as pro-inflammatory because upon stimulation produce TNF-...

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Bibliographic Details
Published in:Scandinavian journal of immunology 2008-02, Vol.67 (2), p.152-159
Main Authors: Skrzeczyńska-Moncznik, J, Bzowska, M, Lo[double acute accent]seke, S, Grage-Griebenow, E, Zembala, M, Pryjma, J
Format: Article
Language:English
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Summary:Based on CD14 and CD16 expression, human peripheral blood monocytes (MO) can be divided into a major CD14high CD16⁻ population and two minor CD14high CD16⁺ and CD14dim CD16⁺ subpopulations. CD14dim CD16⁺ MO are well characterized and regarded as pro-inflammatory because upon stimulation produce TNF-α but little, if any, IL-10. By contrast, little is known about CD14high CD16⁺ MO. We investigated the surface expression of selected determinants by CD16⁺ MO subpopulations, cytokine production, phagocytosis and antigen presentation. We found that both CD16⁺ subpopulations had a higher expression of HLA-DR, CD86, CD54 and a lower expression of CD64 than CD14high CD16⁻ population. In addition, CD14high CD16⁺ MO showed a higher expression of CD11b and TLR4 than CD14dim CD16⁺ and CD14high CD16⁻ subpopulations. CD14high CD16⁺ MO exhibited an increased phagocytic activity and a decreased antigen presentation in comparison with CD14dim CD16⁺. As expected, lipopolysaccharide (LPS)-stimulated CD14dim CD16⁺ MO produced TNF-α but little IL-10. By contrast, LPS-stimulated CD14high CD16⁺ subpopulation produced significantly more IL-10 than CD14dim CD16⁺ and CD14high CD16⁻ MO. In conclusion, our data show that human peripheral blood CD16⁺ MO are heterogeneous in function and consist of two subpopulations: CD14dim CD16⁺ pro-inflammatory and CD14high CD16⁺ with anti-inflammatory potential.
ISSN:0300-9475
1365-3083
DOI:10.1111/j.1365-3083.2007.02051.x