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Electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo
Electrospinning can be used to mimic the architecture of an acellular nerve graft, combining microfibers for guidance, and pores for cellular infiltration. We made electrospun nerve guides, from polycaprolactone (PCL) or poly-L-lactic acid (PLLA), with aligned fibers along the insides of the channel...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233209/ https://www.ncbi.nlm.nih.gov/pubmed/30425260 http://dx.doi.org/10.1038/s41598-018-34699-8 |
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author | Frost, Hanna K. Andersson, Tomas Johansson, Sebastian Englund-Johansson, U. Ekström, Per Dahlin, Lars B. Johansson, Fredrik |
author_facet | Frost, Hanna K. Andersson, Tomas Johansson, Sebastian Englund-Johansson, U. Ekström, Per Dahlin, Lars B. Johansson, Fredrik |
author_sort | Frost, Hanna K. |
collection | PubMed |
description | Electrospinning can be used to mimic the architecture of an acellular nerve graft, combining microfibers for guidance, and pores for cellular infiltration. We made electrospun nerve guides, from polycaprolactone (PCL) or poly-L-lactic acid (PLLA), with aligned fibers along the insides of the channels and random fibers around them. We bridged a 10 mm rat sciatic nerve defect with the guides, and, in selected groups, added a cell transplant derived from autologous stromal vascular fraction (SVF). For control, we compared to hollow silicone tubes; or autologous nerve grafts. PCL nerve guides had a high degree of autotomy (8/43 rats), a negative indicator with respect to future usefulness, while PLLA supported axonal regeneration, but did not outperform autologous nerve grafts. Transplanted cells survived in the PLLA nerve guides, but axonal regeneration was not enhanced as compared to nerve guides alone. The inflammatory response was partially enhanced by the transplanted cells in PLLA nerve grafts; Schwann cells were poorly distributed compared to nerve guide without cells. Tailor-made electrospun nerve guides support axonal regeneration in vivo, and can act as vehicles for co-transplanted cells. Our results motivate further studies exploring novel nerve guides and the effect of stromal cell-derived factors on nerve generation. |
format | Online Article Text |
id | pubmed-6233209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62332092018-11-28 Electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo Frost, Hanna K. Andersson, Tomas Johansson, Sebastian Englund-Johansson, U. Ekström, Per Dahlin, Lars B. Johansson, Fredrik Sci Rep Article Electrospinning can be used to mimic the architecture of an acellular nerve graft, combining microfibers for guidance, and pores for cellular infiltration. We made electrospun nerve guides, from polycaprolactone (PCL) or poly-L-lactic acid (PLLA), with aligned fibers along the insides of the channels and random fibers around them. We bridged a 10 mm rat sciatic nerve defect with the guides, and, in selected groups, added a cell transplant derived from autologous stromal vascular fraction (SVF). For control, we compared to hollow silicone tubes; or autologous nerve grafts. PCL nerve guides had a high degree of autotomy (8/43 rats), a negative indicator with respect to future usefulness, while PLLA supported axonal regeneration, but did not outperform autologous nerve grafts. Transplanted cells survived in the PLLA nerve guides, but axonal regeneration was not enhanced as compared to nerve guides alone. The inflammatory response was partially enhanced by the transplanted cells in PLLA nerve grafts; Schwann cells were poorly distributed compared to nerve guide without cells. Tailor-made electrospun nerve guides support axonal regeneration in vivo, and can act as vehicles for co-transplanted cells. Our results motivate further studies exploring novel nerve guides and the effect of stromal cell-derived factors on nerve generation. Nature Publishing Group UK 2018-11-13 /pmc/articles/PMC6233209/ /pubmed/30425260 http://dx.doi.org/10.1038/s41598-018-34699-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Frost, Hanna K. Andersson, Tomas Johansson, Sebastian Englund-Johansson, U. Ekström, Per Dahlin, Lars B. Johansson, Fredrik Electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo |
title | Electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo |
title_full | Electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo |
title_fullStr | Electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo |
title_full_unstemmed | Electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo |
title_short | Electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo |
title_sort | electrospun nerve guide conduits have the potential to bridge peripheral nerve injuries in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233209/ https://www.ncbi.nlm.nih.gov/pubmed/30425260 http://dx.doi.org/10.1038/s41598-018-34699-8 |
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