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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...

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Autores principales: Zhou, Chan, Li, Jin, You, Huajian, Lv, Jinfeng, Yang, Jinlong, Liu, Bin
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
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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.
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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
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