Macrophage Receptors

Macrophage receptors are cell-surface and intracellular proteins that detect microbes, damaged cells, antibodies, complement fragments, and signaling molecules, allowing macrophages to coordinate immune defense and tissue maintenance. When a ligand binds its receptor, the interaction can activate intracellular signaling pathways that promote phagocytosis, secretion of inflammatory mediators, antigen presentation, or changes in macrophage activation. Major receptor groups include pattern-recognition, Fc, complement, scavenger, and cytokine receptors, each contributing to distinct cellular responses. Studying these receptors helps explain host defense, inflammation, tissue repair, and disease progression, while supporting research into vaccines, immunotherapies, infectious disease treatments, and targeted drug delivery.

Macrophage Receptors - Related Videos

Research

JoVE EoE - Bacterial Pathogenesis and Host Interactions

Analysis of Macrophage Receptor Interactions with Pathogenic Bacteria Using Flow Cytometry

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2026

Source: Barbero, A. M., et al. Fluorescence Assays for the Study of Mycobacterium tuberculosis Interaction with the Immune Receptor SLAMF1. J. Vis. Exp. (2025)This video demonstrates the procedure for labeling host immune receptors that bind bacterial surface antigens, enabling their detection through flow cytometry.

Fluorescence-Based Assay for Investigating Macrophage Receptor Interactions with Bacterial Antigens

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2026

Source: Barbero, A. M., et.al. Fluorescence Assays for the Study of Mycobacterium tuberculosis Interaction with the Immune Receptor SLAMF1. J. Vis. Exp. ( (2025)This video demonstrates a fluorescence-based assay to study the interaction between a macrophage receptor and Mycobacterium tuberculosis antigens. Fluorescently labeled antigens on a coverslip are incubated with macrophage protein extracts, cross-linked, antibody-labeled, and visualized by overlapping fluorescence signals.

Isolation of Murine Peritoneal Macrophages to Carry Out Gene Expression Analysis Upon Toll-like Receptors Stimulation

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Cited by 78 •

2015

We describe here a simple protocol to isolate murine peritoneal macrophages. This procedure is followed by RNA extraction to carry out gene expression analysis upon Toll-like receptors stimulation.

Investigation of Macrophage Polarization Using Bone Marrow Derived Macrophages

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Cited by 326 •

2013

The article describes a readily easy adaptive in vitro model to investigate macrophage polarization. In the presence of GM-CSF/M-CSF, hematopoietic stem/progenitor cells from the bone marrow are directed into monocytic differentiation, followed by M1 or M2 stimulation. The activation status can be tracked by changes in cell surface antigens, gene expression and cell signaling pathways.

In Vitro Culture and Differentiation of Primary Monocytes into Macrophages

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2025

This video demonstrates the priming of primary monocytes into macrophages. Primary human monocytes can be isolated and differentiated to an M1-like pro-inflammatory phenotype using the granulocyte-macrophage colony-stimulating factor (GM-CSF) or to an M2-like anti-inflammatory phenotype using the macrophage colony-stimulating factor (M-CSF).

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