Neuron-macrophage Co-culture

Neuron-macrophage co-culture is an in vitro model that grows neurons and macrophages together to study communication between the nervous and immune systems. In this system, soluble signaling molecules, cell contact, and changes in the local culture environment allow macrophages to influence neuronal survival, function, and inflammatory responses, while neurons can alter macrophage activation. Neuroscience researchers use co-culture experiments to investigate neuroinflammation, injury responses, and neuron-immune interactions under controlled conditions. The model can also support evaluation of disease mechanisms and potential therapies, providing a bridge between simplified cell studies and more complex tissue or animal systems.

Neuron-macrophage Co-culture - Related Videos

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JoVE EoE - Neuronal Culture Techniques

Developing a Neuron and Macrophage Coculture In Vitro

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2025

This video shows the co-culturing of murine dorsal root ganglion neurons and macrophages. Neurons are seeded on a coated plate, while macrophages are collected from an euthanized mouse, treated, and added to the culture insert. Treatment with db-cAMP activates neurons and prompts macrophages to adopt a pro-regenerative phenotype to support neuronal outgrowth.

Using a Macrophage Conditioned Medium to Promote Neuron Extensions

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2025

This video demonstrates an assay for promoting the growth of neuron projections known as neurite outgrowth using the macrophage-conditioned medium. Co-culture neurons and macrophages with cAMP and harvest the macrophage-derived conditioned medium. Growing the neurons with the conditioned medium promotes neurite outgrowths. These outgrowths are fluorescently labeled and visualized using a fluorescence microscope.

Assessment of Leishmania Virulence within Cultured Macrophages

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2025

This video investigates Leishmania's virulence by treating macrophages with metacyclic promastigotes, resulting in the formation of intracellular amastigotes. The confirmation of Leishmania's virulence is achieved through nucleic acid fluorescent dye staining. This insight can contribute to the development of new therapies for leishmaniasis.

Culture of Macrophage Colony-stimulating Factor Differentiated Human Monocyte-derived Macrophages

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Cited by 58 •

2016

A protocol is presented for cell culture of macrophage colony-stimulating factor (M-CSF) differentiated human monocyte-derived macrophages. The protocol utilizes cryopreservation of monocytes coupled with their bulk differentiation into macrophages. Then harvested macrophages can then be seeded into culture wells at required cell densities for carrying out experiments.

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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