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Human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury
Treatment and functional reconstruction after central nervous system injury is a major medical and social challenge. An increasing number of researchers are attempting to use neural stem cells combined with artificial scaffold materials, such as fibroin, for nerve repair. However, such approaches ar...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116849/ https://www.ncbi.nlm.nih.gov/pubmed/27904501 http://dx.doi.org/10.4103/1673-5374.193249 |
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author | Wang, Ting-gang Xu, Jie Zhu, Ai-hua Lu, Hua Miao, Zong-ning Zhao, Peng Hui, Guo-zhen Wu, Wei-jiang |
author_facet | Wang, Ting-gang Xu, Jie Zhu, Ai-hua Lu, Hua Miao, Zong-ning Zhao, Peng Hui, Guo-zhen Wu, Wei-jiang |
author_sort | Wang, Ting-gang |
collection | PubMed |
description | Treatment and functional reconstruction after central nervous system injury is a major medical and social challenge. An increasing number of researchers are attempting to use neural stem cells combined with artificial scaffold materials, such as fibroin, for nerve repair. However, such approaches are challenged by ethical and practical issues. Amniotic tissue, a clinical waste product, is abundant, and amniotic epithelial cells are pluripotent, have low immunogenicity, and are not the subject of ethical debate. We hypothesized that amniotic epithelial cells combined with silk fibroin scaffolds would be conducive to the repair of spinal cord injury. To test this, we isolated and cultured amniotic epithelial cells, and constructed complexes of these cells and silk fibroin scaffolds. Implantation of the cell-scaffold complex into a rat model of spinal cord injury resulted in a smaller glial scar in the damaged cord tissue than in model rats that received a blank scaffold, or amniotic epithelial cells alone. In addition to a milder local immunological reaction, the rats showed less inflammatory cell infiltration at the transplant site, milder host-versus-graft reaction, and a marked improvement in motor function. These findings confirm that the transplantation of amniotic epithelial cells combined with silk fibroin scaffold can promote the repair of spinal cord injury. Silk fibroin scaffold can provide a good nerve regeneration microenvironment for amniotic epithelial cells. |
format | Online Article Text |
id | pubmed-5116849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51168492016-11-30 Human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury Wang, Ting-gang Xu, Jie Zhu, Ai-hua Lu, Hua Miao, Zong-ning Zhao, Peng Hui, Guo-zhen Wu, Wei-jiang Neural Regen Res Research Article Treatment and functional reconstruction after central nervous system injury is a major medical and social challenge. An increasing number of researchers are attempting to use neural stem cells combined with artificial scaffold materials, such as fibroin, for nerve repair. However, such approaches are challenged by ethical and practical issues. Amniotic tissue, a clinical waste product, is abundant, and amniotic epithelial cells are pluripotent, have low immunogenicity, and are not the subject of ethical debate. We hypothesized that amniotic epithelial cells combined with silk fibroin scaffolds would be conducive to the repair of spinal cord injury. To test this, we isolated and cultured amniotic epithelial cells, and constructed complexes of these cells and silk fibroin scaffolds. Implantation of the cell-scaffold complex into a rat model of spinal cord injury resulted in a smaller glial scar in the damaged cord tissue than in model rats that received a blank scaffold, or amniotic epithelial cells alone. In addition to a milder local immunological reaction, the rats showed less inflammatory cell infiltration at the transplant site, milder host-versus-graft reaction, and a marked improvement in motor function. These findings confirm that the transplantation of amniotic epithelial cells combined with silk fibroin scaffold can promote the repair of spinal cord injury. Silk fibroin scaffold can provide a good nerve regeneration microenvironment for amniotic epithelial cells. Medknow Publications & Media Pvt Ltd 2016-10 /pmc/articles/PMC5116849/ /pubmed/27904501 http://dx.doi.org/10.4103/1673-5374.193249 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Wang, Ting-gang Xu, Jie Zhu, Ai-hua Lu, Hua Miao, Zong-ning Zhao, Peng Hui, Guo-zhen Wu, Wei-jiang Human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury |
title | Human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury |
title_full | Human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury |
title_fullStr | Human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury |
title_full_unstemmed | Human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury |
title_short | Human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury |
title_sort | human amniotic epithelial cells combined with silk fibroin scaffold in the repair of spinal cord injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116849/ https://www.ncbi.nlm.nih.gov/pubmed/27904501 http://dx.doi.org/10.4103/1673-5374.193249 |
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