Gfp Labeled Macrophages

GFP-labeled macrophages are immune cells engineered or selected to express green fluorescent protein (GFP), enabling researchers to visualize their location, movement, and behavior in living tissues. GFP fluorescence arises when the expressed protein absorbs excitation light and emits green light, allowing macrophages to be tracked by fluorescence microscopy without additional staining. In developmental biology, these labeled cells help reveal how macrophages migrate through developing organs, interact with other cells, and contribute to tissue remodeling and immune surveillance. The approach supports real-time analysis of cell dynamics and links macrophage behavior to normal development, inflammation, and disease-related changes.

Gfp Labeled Macrophages - Related Videos

Research

JoVE Journal - Biology
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Live Imaging of GFP-labeled Proteins in Drosophila Oocytes

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Cited by 5 •

2013

A protocol for live imaging of GFP-tagged proteins or autofluorescent structures in individual Drosophila oocytes is described.

Research

JoVE EoE - Colorectal Cancer

CRC Organoid Cell Labeling: A Method to Generate GFP Lentivirus-transduced Colorectal Cancer Organoid Cells

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2023

This video describes the technique of generating CRC organoids transduced by GFP lentiviral particles for enabling fluorescent imaging. These GFP labeled organoids, when placed in animal models, help to study tumor invasion and metastasis.

Research

JoVE Journal - Immunology and Infection

Time-Lapse Imaging of Antibody-Driven Macrophage Phagocytosis of Green Fluorescence Protein–Labeled Triple-Negative Breast Cancer Cells

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2026

This protocol describes a time-lapse live-cell imaging method to visualize antibody-dependent macrophage phagocytosis of green fluorescent protein–labeled triple-negative breast cancer cells using peripheral blood mononuclear cell–derived macrophages and an automated microscope.

Real-Time Label-Free Imaging and Quantitative Analysis of Macrophage Morphodynamics Using Optical Diffraction Tomography

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2026

This protocol describes a label-free optical diffraction tomography-based workflow for real-time imaging and quantitative analysis of macrophage morphodynamics. The method enables continuous tracking of single-cell morphology and migration, providing time-resolved measurements of projected area, perimeter, and average migration speed during long-term live-cell imaging.

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.

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