After Nerve Injury, Lineage Tracing Shows That Myelin and Remak Schwann Cells Elongate Extensively and Branch to Form Repair Schwann Cells, Which Shorten Radically on Remyelination

There is consensus that distal to peripheral nerve injury, myelin and Remak cells reorganize to form cellular columns, Bungner9s bands, which are indispensable for regeneration. Yet knowledge of the structure of these regeneration tracks has not advanced for decades, and the structure of the cells that form them, denervated or repair Schwann cells, remains obscure. Furthermore, the origin of these cells from myelin and Remak cells, and their ability to give rise to myelin cells after regeneration has not been directly demonstrated, although these conversions are believed to be central to nerve repair. Using genetic lineage-tracing and scanning block face electron microscopy, we show that injury of sciatic nerves from mice of either sex triggers extensive and unexpected Schwann cell elongation and branching to form long parallel processes. Repair cells are two-to-three fold longer than myelin and Remak cells, and seven to 10 fold longer than immature Schwann cells. Remarkably, when repair cells transit back to myelinating cells they shorten about seven fold, to generate the typically short internodes of regenerated nerves. The present experiments define novel morphological transitions in injured nerves, and show that repair Schwann cells have a cell-type specific structure, which differentiates them from other cells in the Schwann cell lineage. They also provide the first direct evidence using genetic lineage-tracing, for two basic assumptions in Schwann cell biology, namely that myelin and Remak cells generate the elongated cells that build Bungner bands in injured nerves, and that such cells can transform to myelin cells after regeneration. SIGNIFICANCE STATEMENT After injury to peripheral nerves, the myelin and Remak Schwann cells distal to the injury site reorganize and modify their properties to form cells that support the survival of injured neurons, promote axon growth, remove myelin-associated growth inhibitors and guide regenerating axons to their targets. We show that the generation of these repair-supportive Schwann cells involves an extensive cellular elongation and branching, often to form long parallel processes. This generates a distinctive repair cell morphology that is favourable for the formation of the regeneration tracks that are essential for nerve repair. Re-myelination, conversely, involves a striking cell shortening to form the typical short myelin cells of regenerated nerves. We also provide evidence for direct lineage relationships between repair cells and myelin and Remak cells of uninjured nerves on the one hand, and re-myelinating cells in regenerated nerves on the other.