Cargando…
Cell activity during peripheral nerve defect repair process using a nerve scaffold
Peripheral nerve defects, but not artificial nerves, are repaired by endogenous cells. We examined cell activity during the repair process in the presence of autologous nerves and artificial preparations in order to guide future artificial nerve fabrication. PLGA tubes, nerve scaffolds comprising a...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768366/ https://www.ncbi.nlm.nih.gov/pubmed/29371949 http://dx.doi.org/10.18632/oncotarget.22978 |
_version_ | 1783292692281688064 |
---|---|
author | Zhou, Chan Li, Jin You, Huajian Lv, Jinfeng Yang, Jinlong Liu, Bin |
author_facet | Zhou, Chan Li, Jin You, Huajian Lv, Jinfeng Yang, Jinlong Liu, Bin |
author_sort | Zhou, Chan |
collection | PubMed |
description | Peripheral nerve defects, but not artificial nerves, are repaired by endogenous cells. We examined cell activity during the repair process in the presence of autologous nerves and artificial preparations in order to guide future artificial nerve fabrication. PLGA tubes, nerve scaffolds comprising a PLGA tube plus 6,000 fibroin fibers, or autologous nerves were implanted into 10 mm rat sciatic nerve defects (n = 60 per group). Over a period of 1-20 weeks after nerve grafting, sections were stained and imaged to distinguish the cell types present and we quantified the recovery of motor and sensory function in the surgically implanted limb. We observed a decreasing trend in inflammatory cell and fibroblast counts over time which ranked in magnitude as: (PLGA group > nerve scaffold > autologous nerve> sham) and an opposite trend in Schwann cell counts. Differences in withdrawal time from hot water and static sciatic index (SSI) indicated that, after repair, sensory and motor function were best in the sham group, followed by the autologous group, the nerve scaffold group, and the PLGA group. These findings indicate that the inflammatory reaction is significant in the first two weeks after nerve grafting, followed by the rebirth of fibroblasts and Schwann cells, which guide axon regeneration. This inflammatory response was a fundamental stage of peripheral defect repair, but a weaker inflammatory response corresponded to better recovery of sensorimotor functional. |
format | Online Article Text |
id | pubmed-5768366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57683662018-01-25 Cell activity during peripheral nerve defect repair process using a nerve scaffold Zhou, Chan Li, Jin You, Huajian Lv, Jinfeng Yang, Jinlong Liu, Bin Oncotarget Research Paper Peripheral nerve defects, but not artificial nerves, are repaired by endogenous cells. We examined cell activity during the repair process in the presence of autologous nerves and artificial preparations in order to guide future artificial nerve fabrication. PLGA tubes, nerve scaffolds comprising a PLGA tube plus 6,000 fibroin fibers, or autologous nerves were implanted into 10 mm rat sciatic nerve defects (n = 60 per group). Over a period of 1-20 weeks after nerve grafting, sections were stained and imaged to distinguish the cell types present and we quantified the recovery of motor and sensory function in the surgically implanted limb. We observed a decreasing trend in inflammatory cell and fibroblast counts over time which ranked in magnitude as: (PLGA group > nerve scaffold > autologous nerve> sham) and an opposite trend in Schwann cell counts. Differences in withdrawal time from hot water and static sciatic index (SSI) indicated that, after repair, sensory and motor function were best in the sham group, followed by the autologous group, the nerve scaffold group, and the PLGA group. These findings indicate that the inflammatory reaction is significant in the first two weeks after nerve grafting, followed by the rebirth of fibroblasts and Schwann cells, which guide axon regeneration. This inflammatory response was a fundamental stage of peripheral defect repair, but a weaker inflammatory response corresponded to better recovery of sensorimotor functional. Impact Journals LLC 2017-12-05 /pmc/articles/PMC5768366/ /pubmed/29371949 http://dx.doi.org/10.18632/oncotarget.22978 Text en Copyright: © 2017 Zhou et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Zhou, Chan Li, Jin You, Huajian Lv, Jinfeng Yang, Jinlong Liu, Bin Cell activity during peripheral nerve defect repair process using a nerve scaffold |
title | Cell activity during peripheral nerve defect repair process using a nerve scaffold |
title_full | Cell activity during peripheral nerve defect repair process using a nerve scaffold |
title_fullStr | Cell activity during peripheral nerve defect repair process using a nerve scaffold |
title_full_unstemmed | Cell activity during peripheral nerve defect repair process using a nerve scaffold |
title_short | Cell activity during peripheral nerve defect repair process using a nerve scaffold |
title_sort | cell activity during peripheral nerve defect repair process using a nerve scaffold |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768366/ https://www.ncbi.nlm.nih.gov/pubmed/29371949 http://dx.doi.org/10.18632/oncotarget.22978 |
work_keys_str_mv | AT zhouchan cellactivityduringperipheralnervedefectrepairprocessusinganervescaffold AT lijin cellactivityduringperipheralnervedefectrepairprocessusinganervescaffold AT youhuajian cellactivityduringperipheralnervedefectrepairprocessusinganervescaffold AT lvjinfeng cellactivityduringperipheralnervedefectrepairprocessusinganervescaffold AT yangjinlong cellactivityduringperipheralnervedefectrepairprocessusinganervescaffold AT liubin cellactivityduringperipheralnervedefectrepairprocessusinganervescaffold |