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Updated: Oct 17, 2026

Mesenchymal Stem Cell Regulation of Macrophage Phagocytosis; Quantitation and Imaging
Published on: July 16, 2021
Regulation of scavenger receptor CD163 expression in human monocytes and macrophages by pro- and antiinflammatory
1Institut für Klinische Chemie und Laboratoriumsmedizin, Klinikum der Universität Regensburg, Germany.
Abstract:
CD163, also referred to as M130, a member of the scavenger receptor cysteine-rich family (SRCR) is exclusively expressed on cells of the monocyte lineage. In freshly isolated monocytes the CD14bright CD16+ monocyte subset revealed the highest expression of CD163 among all monocyte subsets. CD163 mRNA and protein expression is up-regulated during macrophage colony-stimulating factor (M-CSF)-dependent phagocytic differentiation of human blood monocytes. In contrast, monocytic cells treated with GM-CSF and interleukin-4 (IL-4) for dendritic differentiation down-regulate this antigen. CD163 expression is also suppressed by proinflammatory mediators like lipopolysaccharide (LPS), interferon-gamma (IFN-gamma), and tumor necrosis factor alpha, whereas IL-6 and the antiinflammatory cytokine interleukin-10 (IL-10) strongly up-regulate CD163 mRNA in monocytes and macrophages. The effects of the immunosuppressants dexamethasone, cyclosporin A (CA), and cortisol differ in their capacity to influence CD163 mRNA levels. Our results demonstrate that CD163 expression in monocytes/macrophages is regulated by proinflammatory and antiinflammatory mediators. This expression pattern implies a functional role of CD 163 in the antiinflammatory response of monocytes.
Insights
CD163, a scavenger receptor on monocytes, is upregulated during phagocytic differentiation and by anti-inflammatory cytokines like IL-10. Its expression is suppressed by pro-inflammatory mediators, suggesting a role in the anti-inflammatory response.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- CD163 (M130) is a scavenger receptor cysteine-rich (SRCR) family member exclusively expressed on monocytes.
- Highest CD163 expression is observed in CD14bright CD16+ monocyte subsets.
- Monocyte differentiation and inflammatory status significantly impact CD163 expression.
Purpose of the Study:
- To investigate the regulation of CD163 expression in human monocytes and macrophages.
- To determine the influence of various cytokines and mediators on CD163 mRNA and protein levels.
- To elucidate the functional role of CD163 in the context of monocyte-derived inflammatory responses.
Main Methods:
- Analysis of CD163 expression in different monocyte subsets.
- Assessment of CD163 mRNA and protein changes during M-CSF and GM-CSF/IL-4 induced differentiation.
- Treatment of monocytes/macrophages with pro-inflammatory (LPS, IFN-γ, TNF-α), anti-inflammatory (IL-6, IL-10), and immunosuppressive agents (dexamethasone, cyclosporin A, cortisol).
Main Results:
- CD163 expression is upregulated during M-CSF-dependent phagocytic differentiation.
- Dendritic differentiation induced by GM-CSF/IL-4 downregulates CD163.
- Pro-inflammatory mediators (LPS, IFN-γ, TNF-α) suppress CD163, while IL-6 and IL-10 strongly upregulate it.
- Immunosuppressants show variable effects on CD163 mRNA levels.
Conclusions:
- CD163 expression in monocytes/macrophages is dynamically regulated by both pro-inflammatory and anti-inflammatory mediators.
- The observed expression pattern suggests a significant functional role for CD163 in mediating the anti-inflammatory response of monocytes.
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