Functional recovery following traumatic spinal cord injury mediated by a unique polymer scaffold seeded with neural stem cells
dc.contributor.author | Teng, Yang D. | |
dc.contributor.author | Lavik, Erin | |
dc.contributor.author | Qu, Xianlu | |
dc.contributor.author | Park, Kook I. | |
dc.contributor.author | Ourednik, Jitka | |
dc.contributor.author | Zurakowski, David | |
dc.contributor.author | Langer, Robert | |
dc.contributor.author | Snyder, Evan Y. | |
dc.date.accessioned | 2021-03-19T16:59:31Z | |
dc.date.available | 2021-03-19T16:59:31Z | |
dc.date.issued | 2002-03-05 | |
dc.description | Proceedings of the National Academy of Sciences Mar 2002, 99 (5) 3024-3029 | en_US |
dc.description.abstract | To better direct repair following spinal cord injury (SCI), we designed an implant modeled after the intact spinal cord consisting of a multicomponent polymer scaffold seeded with neural stem cells. Implantation of the scaffold–neural stem cells unit into an adult rat hemisection model of SCI promoted long-term improvement in function (persistent for 1 year in some animals) relative to a lesion-control group. At 70 days postinjury, animals implanted with scaffold-plus-cells exhibited coordinated, weight-bearing hindlimb stepping. Histology and immunocytochemical analysis suggested that this recovery might be attributable partly to a reduction in tissue loss from secondary injury processes as well as in diminished glial scarring. Tract tracing demonstrated corticospinal tract fibers passing through the injury epicenter to the caudal cord, a phenomenon not present in untreated groups. Together with evidence of enhanced local GAP-43 expression not seen in controls, these findings suggest a possible regeneration component. These results may suggest a new approach to SCI and, more broadly, may serve as a prototype for multidisciplinary strategies against complex neurological problems | en_US |
dc.description.sponsorship | We thank Umberto DeGirolami, Marion Slaney, Ali Shafarae, Karen Fu, Daniel Kohane, Larry Benowitz, and Carl Lagenaur for their assistance. This work was supported in part by Project ALS, National Institutes of Health 1-R21-NS41999-01, International Institute for Research in Paraplegia, and the A-T Children's Project, as well as a Harvard School of Dental Medicine/Massachusetts Institute of Technology National Institute of Dental and Craniofacial Research Training Grant in Biomaterials (to E.B.L.). R.L. holds equity in GMP Companies, which holds certain patents in this area. | en_US |
dc.description.uri | https://www.pnas.org/content/99/5/3024.long | en_US |
dc.format.extent | 7 pages | en_US |
dc.genre | conference papers and proceedings | en_US |
dc.identifier | doi:10.13016/m21nvy-be8w | |
dc.identifier.citation | Yang D. Teng, Erin B. Lavik, Xianlu Qu, Kook I. Park, Jitka Ourednik, David Zurakowski, Robert Langer, Evan Y. Snyder, Functional recovery following traumatic spinal cord injury mediated by a unique polymer scaffold seeded with neural stem cells, Proceedings of the National Academy of Sciences Mar 2002, 99 (5) 3024-3029; DOI: 10.1073/pnas.052678899 | en_US |
dc.identifier.uri | https://doi.org/10.1073/pnas.052678899 | |
dc.identifier.uri | http://hdl.handle.net/11603/21193 | |
dc.language.iso | en_US | en_US |
dc.publisher | PNAS | en_US |
dc.relation.isAvailableAt | The University of Maryland, Baltimore County (UMBC) | |
dc.relation.ispartof | UMBC Chemical, Biochemical & Environmental Engineering Department Collection | |
dc.rights | This item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author. | |
dc.subject | spinal cord injury | |
dc.subject | neural stem cells | |
dc.subject | multicomponent polymer scaffold | |
dc.subject | functional long-term improvement | |
dc.title | Functional recovery following traumatic spinal cord injury mediated by a unique polymer scaffold seeded with neural stem cells | en_US |
dc.type | Text | en_US |
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