Regulation of scavenger receptor CD163 expression in human monocytes and macrophages by pro- and antiinflammatory stimuli
Регуляция экспрессии скавенджер-рецептора CD163 в моноцитах и макрофагах человека провоспалительными и противовоспалительными стимулами
2000-01-01
SCID: 54.1/m4adq62f
Discuss with AI
CD163 expressionM-CSF-dependent phagocytic differentiationhuman monocytes and macrophagesinterleukin-10proinflammatory mediators
Figures from the paper
Abstract (AI)
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.
Key Findings
1
CD163 is most highly expressed in the CD14bright CD16+ human monocyte subset.
2
CD163 regulation by dexamethasone, cyclosporin A, and cortisol differs among these immunosuppressive agents, supporting a role for CD163 in anti-inflammatory monocyte responses.
3
GM-CSF plus IL-4 treatment for dendritic-cell differentiation down-regulates CD163 expression.
4
M-CSF-driven phagocytic differentiation increases CD163 mRNA and protein expression in human blood monocytes.
5
Proinflammatory LPS, IFN-γ, and TNF-α suppress CD163 expression, whereas IL-6 and IL-10 strongly increase CD163 mRNA in monocytes and macrophages.
Research Object
CD163 expression in human monocytes and macrophages
Research Subject
Regulation of CD163 mRNA and protein expression by monocyte-subset identity, macrophage and dendritic differentiation, proinflammatory and antiinflammatory mediators, and immunosuppressants
Publication Details
Publication Date
2000-01-01
Journal
Publisher
ISSN
Access Type
Author Information
Download PDF
Subscribe to digest