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Updated: Jul 31, 2026

Bone Marrow-derived Macrophage Production
Published on: November 22, 2013
Macrophage response to microbial pathogens: modulation of the expression of adhesion, CD14, and MHC class II
Abstract:
The ability of inactivated viruses, bacteria, protozoa and fungi to modulate the expression of CD14, CD49d, CD49f, CD11a (LFA-1), and CD54 (ICAM-1) molecules in unprimed bone marrow-derived mononuclear phagocytes (BMM phi) was investigated by means of flow cytometry. Incubation with bacterial agents resulted in the large majority of experimental situations in enhanced expression of these macrophage surface molecules. In contrast, viruses and fungi down-regulated the expression of several adhesion receptors, especially integrins. Amplification of MHC class II expression triggered in macrophages by interferon gamma was clearly inhibited by viruses, bacteria, protozoa and fungi. The findings explain earlier results showing that, under the same experimental conditions, bacterial agents are, for the most part, potent stimulators of secretory and cell-mediated macrophage activities while viruses, protozoa and fungi are poor in this respect.
Insights
Microbial agents like bacteria, viruses, and fungi affect macrophage surface molecule expression differently. Bacteria generally enhance expression, while viruses and fungi down-regulate it, impacting immune responses.
Area of Science:
- Immunology
- Microbiology
- Cell Biology
Background:
- Macrophage surface molecules play critical roles in immune cell interactions and activation.
- Different microbial components can elicit distinct responses from immune cells.
- Understanding these interactions is key to developing immunomodulatory therapies.
Purpose of the Study:
- To investigate how inactivated microbial agents (viruses, bacteria, protozoa, fungi) modulate specific macrophage surface molecules.
- To compare the effects of different microbial types on macrophage activation markers.
- To correlate observed surface molecule changes with known macrophage functional responses.
Main Methods:
- Utilized flow cytometry to analyze the expression of CD14, CD49d, CD49f, CD11a (LFA-1), and CD54 (ICAM-1) on bone marrow-derived mononuclear phagocytes (BMM phi).
- Incubated BMM phi with inactivated viruses, bacteria, protozoa, and fungi.
- Assessed the impact on Major Histocompatibility Complex (MHC) class II expression amplification by interferon gamma.
Main Results:
- Bacterial agents predominantly enhanced the expression of macrophage surface molecules.
- Viruses and fungi significantly down-regulated several adhesion receptors, particularly integrins.
- All tested microbial agents inhibited the interferon gamma-induced amplification of MHC class II expression.
Conclusions:
- Distinct microbial types differentially modulate macrophage surface molecule expression.
- Bacterial agents are potent stimulators of macrophage secretory and cell-mediated activities.
- Viruses, protozoa, and fungi are less effective stimulators, likely due to down-regulation of key surface receptors.
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