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A nerve conduit filled with Wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration
AIMS: Peripheral nerve injury is a significant clinical problem with a substantial impact on quality of life, for which no optimal treatment has been found. This study aimed to analyze the effect and mechanism of Wnt5a‐loaded fibrin hydrogel on a 10‐mm rat sciatic nerve defect. METHODS: The Wnt5a‐lo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673702/ https://www.ncbi.nlm.nih.gov/pubmed/34729936 http://dx.doi.org/10.1111/cns.13752 |
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author | Liu, Yi‐jun Chen, Xiao‐feng Zhou, Li‐ping Rao, Feng Zhang, Dian‐ying Wang, Yan‐hua |
author_facet | Liu, Yi‐jun Chen, Xiao‐feng Zhou, Li‐ping Rao, Feng Zhang, Dian‐ying Wang, Yan‐hua |
author_sort | Liu, Yi‐jun |
collection | PubMed |
description | AIMS: Peripheral nerve injury is a significant clinical problem with a substantial impact on quality of life, for which no optimal treatment has been found. This study aimed to analyze the effect and mechanism of Wnt5a‐loaded fibrin hydrogel on a 10‐mm rat sciatic nerve defect. METHODS: The Wnt5a‐loaded fibrin hydrogel was synthesized by mixing a Wnt5a solution with thrombin and fibrinogen solutions. The loading capacity and release profile of Wnt5a‐loaded fibrin hydrogel and the effect of Wnt5a on Schwann cells were evaluated in vitro. We also assessed the in vivo repair status via histological analysis of the regenerative nerve and gastrocnemius muscle, electrophysiological examination, gait analysis, and muscle wet weight. RESULTS: We developed a nerve conduit filled with Wnt5a‐loaded fibrin hydrogel (Fn) as a sustained‐release system to repair a 10‐mm rat sciatic nerve defect. In vitro, Wnt5a could promote SC proliferation and the gene expression of vascular endothelial growth factor (VEGF), nerve growth factor (NGF), and cholinergic neurotrophic factor (CNTF), as well as the protein secretion of VEGF and NGF. In vivo, the Wnt5a/Fn group was superior to the hollow, fibrin hydrogel, and Wnt5a groups in terms of axonal growth, myelination, electrophysiological recovery, target organ innervation, and motor function recovery 12 weeks after the operation. CONCLUSION: The Wnt5a/Fn nerve conduit can promote peripheral nerve defect regeneration, with potential clinical applications. The mechanism for this may be the facilitation of multiple neurotrophin secretion, combining vascularization and neurotrophic growth cues. |
format | Online Article Text |
id | pubmed-8673702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86737022021-12-22 A nerve conduit filled with Wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration Liu, Yi‐jun Chen, Xiao‐feng Zhou, Li‐ping Rao, Feng Zhang, Dian‐ying Wang, Yan‐hua CNS Neurosci Ther Original Articles AIMS: Peripheral nerve injury is a significant clinical problem with a substantial impact on quality of life, for which no optimal treatment has been found. This study aimed to analyze the effect and mechanism of Wnt5a‐loaded fibrin hydrogel on a 10‐mm rat sciatic nerve defect. METHODS: The Wnt5a‐loaded fibrin hydrogel was synthesized by mixing a Wnt5a solution with thrombin and fibrinogen solutions. The loading capacity and release profile of Wnt5a‐loaded fibrin hydrogel and the effect of Wnt5a on Schwann cells were evaluated in vitro. We also assessed the in vivo repair status via histological analysis of the regenerative nerve and gastrocnemius muscle, electrophysiological examination, gait analysis, and muscle wet weight. RESULTS: We developed a nerve conduit filled with Wnt5a‐loaded fibrin hydrogel (Fn) as a sustained‐release system to repair a 10‐mm rat sciatic nerve defect. In vitro, Wnt5a could promote SC proliferation and the gene expression of vascular endothelial growth factor (VEGF), nerve growth factor (NGF), and cholinergic neurotrophic factor (CNTF), as well as the protein secretion of VEGF and NGF. In vivo, the Wnt5a/Fn group was superior to the hollow, fibrin hydrogel, and Wnt5a groups in terms of axonal growth, myelination, electrophysiological recovery, target organ innervation, and motor function recovery 12 weeks after the operation. CONCLUSION: The Wnt5a/Fn nerve conduit can promote peripheral nerve defect regeneration, with potential clinical applications. The mechanism for this may be the facilitation of multiple neurotrophin secretion, combining vascularization and neurotrophic growth cues. John Wiley and Sons Inc. 2021-11-02 /pmc/articles/PMC8673702/ /pubmed/34729936 http://dx.doi.org/10.1111/cns.13752 Text en © 2021 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Liu, Yi‐jun Chen, Xiao‐feng Zhou, Li‐ping Rao, Feng Zhang, Dian‐ying Wang, Yan‐hua A nerve conduit filled with Wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration |
title | A nerve conduit filled with Wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration |
title_full | A nerve conduit filled with Wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration |
title_fullStr | A nerve conduit filled with Wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration |
title_full_unstemmed | A nerve conduit filled with Wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration |
title_short | A nerve conduit filled with Wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration |
title_sort | nerve conduit filled with wnt5a‐loaded fibrin hydrogels promotes peripheral nerve regeneration |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673702/ https://www.ncbi.nlm.nih.gov/pubmed/34729936 http://dx.doi.org/10.1111/cns.13752 |
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