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.

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.

Dual Labeling of Neural Crest Cells and Blood Vessels Within Chicken Embryos Using ChickGFP Neural Tube Grafting and Carbocyanine Dye DiI Injection

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Cited by 11 •

2015

Here we report dual labeling of neural crest cells and blood vessels using chickGFP neural tube intraspecies grafting combined with intra-vascular DiI injection. This experimental technique allows us to simultaneously visualize and study development of the NCC-derived (enteric) nervous system and the vascular system, during organogenesis.

Assessing Anti-fungal Activity of Isolated Alveolar Macrophages by Confocal Microscopy

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Cited by 3 •

2014

A method to evaluate the ability of isolated mouse alveolar macrophages to control the growth of phagocytosed Aspergillus spores by confocal microscopy.

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