Developing a Neuron and Macrophage Coculture In Vitro
Transcript
Begin with isolated murine dorsal root ganglion neurons in a growth medium.
Seed them onto a polymer-coated multi-well plate to promote neuronal attachment.
Next, take a dissected euthanized mouse and inject ice-cold PBS into its peritoneal cavity.
Gently massage the peritoneum to dislodge macrophages from the peritoneum wall.
Squeeze the mouse to collect the peritoneal fluid and treat it with a lysis buffer to selectively lyse the red blood cells, which appear as contaminants. Centrifuge and resuspend the cells in a culture medium.
Transfer the macrophages to a porous insert positioned within the well containing the cultured neurons.
This co-culture allows neurons and macrophages to be in close proximity.
Treat the co-culture with db-cAMP and incubate to facilitate its entry into the cells. This activates the neurons to secrete the signaling molecules.
These signaling molecules, along with db-cAMP, induce macrophages to adopt a pro-regenerative phenotype and secrete essential factors for neuronal outgrowth.
