• Greg J Duncan, Sohrab B Manesh, Brett J Hilton, Peggy Assinck, Jason R Plemel, and Wolfram Tetzlaff.
• Department of Neurology, Jungers Center for Neurosciences Research, Oregon Health and Science University, Portland, Oregon.
• Glia. 2020 Feb 1; 68 (2): 227-245.

AbstractOligodendrocyte progenitor cells (OPCs) are the most proliferative and dispersed population of progenitor cells in the adult central nervous system, which allows these cells to rapidly respond to damage. Oligodendrocytes and myelin are lost after traumatic spinal cord injury (SCI), compromising efficient conduction and, potentially, the long-term health of axons. In response, OPCs proliferate and then differentiate into new oligodendrocytes and Schwann cells to remyelinate axons. This culminates in highly efficient remyelination following experimental SCI in which nearly all intact demyelinated axons are remyelinated in rodent models. However, myelin regeneration comprises only one role of OPCs following SCI. OPCs contribute to scar formation after SCI and restrict the regeneration of injured axons. Moreover, OPCs alter their gene expression following demyelination, express cytokines and perpetuate the immune response. Here, we review the functional contribution of myelin regeneration and other recently uncovered roles of OPCs and their progeny to repair following SCI.© 2019 Wiley Periodicals, Inc.

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