The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, Florida.
Transplantation of Schwann cells and/or olfactory ensheathing glia into the contused spinal cord: Survival, migration, axon association, and functional recovery
Article first published online: 24 MAY 2007
Copyright © 2007 Wiley-Liss, Inc.
Volume 55, Issue 9, pages 976–1000, July 2007
How to Cite
Pearse, D. D., Sanchez, A. R., Pereira, F. C., Andrade, C. M., Puzis, R., Pressman, Y., Golden, K., Kitay, B. M., Blits, B., Wood, P. M. and Bunge, M. B. (2007), Transplantation of Schwann cells and/or olfactory ensheathing glia into the contused spinal cord: Survival, migration, axon association, and functional recovery. Glia, 55: 976–1000. doi: 10.1002/glia.20490
- Issue published online: 24 MAY 2007
- Article first published online: 24 MAY 2007
- Manuscript Accepted: 9 JAN 2007
- Manuscript Received: 15 SEP 2006
- The Don Misner Foundation. Grant Numbers: NINDS09923, 38665
- The Buoniconti Fund
- The Christopher Reeve Paralysis Foundation
- Bryon Riesch Paralysis and Craig H. Neilson Foundations
- The Miami Project
- spinal cord injury;
- axon growth;
Schwann cells (SCs) and olfactory ensheathing glia (OEG) have shown promise for spinal cord injury repair. We sought their in vivo identification following transplantation into the contused adult rat spinal cord at 1 week post-injury by: (i) DNA in situ hybridization (ISH) with a Y-chromosome specific probe to identify male transplants in female rats and (ii) lentiviral vector-mediated expression of EGFP. Survival, migration, and axon-glia association were quantified from 3 days to 9 weeks post-transplantation. At 3 weeks after transplantation into the lesion, a 60–90% loss of grafted cells was observed. OEG-only grafts survived very poorly within the lesion (<5%); injection outside the lesion led to a 60% survival rate, implying that the injury milieu was hostile to transplanted cells and or prevented their proliferation. At later times post-grafting, p75+/EGFP− cells in the lesion outnumbered EGFP+ cells in all paradigms, evidence of significant host SC infiltration. SCs and OEG injected into the injury failed to migrate from the lesion. Injection of OEG outside of the injury resulted in their migration into the SC-injected injury site, not via normal-appearing host tissue but along the pia or via the central canal. In all paradigms, host axons were seen in association with or ensheathed by transplanted glia. Numerous myelinated axons were found within regions of grafted SCs but not OEG. The current study details the temporal survival, migration, axon association of SCs and OEG, and functional recovery after grafting into the contused spinal cord, research previously complicated due to a lack of quality, long-term markers for cell tracking in vivo. © 2007 Wiley-Liss, Inc.