Schwann cells are axo-protective after injury irrespective of myelination status in mouse Schwann cell-neuron cocultures

Myelinating Schwann cell (SC)-dorsal root ganglion (DRG) neuron cocultures are an important technique for understanding cell-cell signalling and interactions during peripheral nervous system (PNS) myelination, injury, and regeneration. Although methods using rat SCs and neurons or mouse DRG explants are commonplace, there are no established protocols for compartmentalised myelinating cocultures with dissociated mouse cells. There consequently is a need for a coculture protocol that allows separate genetic manipulation of mouse SCs or neurons, or use of cells from different transgenic animals to complement in vivo mouse experiments. However, inducing myelination of dissociated mouse SCs in culture is challenging. Here, we describe a new method to coculture dissociated mouse SCs and DRG neurons in microfluidic chambers and induce robust myelination. Cocultures can be axotomised to study injury and used for drug treatments, and cells can be lentivirally transduced for live imaging. We used this model to investigate axon degeneration after traumatic axotomy and find that SCs, irrespective of myelination status, are axo-protective. At later timepoints after injury, live imaging of cocultures shows that SCs break up, ingest and clear axonal debris.

Automated summary

Coculturing dissociated mouse Schwann cells (SCs) and dorsal root ganglion (DRG) neurons in microfluidic chambers can induce robust myelination and is a valuable technique for studying peripheral nervous system (PNS) myelination, injury, and regeneration. This model allows separate genetic manipulation of mouse SCs or neurons and can be used to complement in vivo mouse experiments. Live imaging of cocultures reveals that SCs are axo-protective and can clear axonal debris after traumatic axotomy.