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Artificial nerve graft constructed by coculture of activated Schwann cells and human hair keratin for repair of peripheral nerve defects

Studies have shown that human hair keratin (HHK) has no antigenicity and excellent mechanical properties. Schwann cells, as unique glial cells in the peripheral nervous system, can be induced by interleukin-1β to secrete nerve growth factor, which promotes neural regeneration. Therefore, HHK with Sc...

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Autores principales: Qin, Han-Jun, Li, Hang, Chen, Jun-Ze, Zhang, Kai-Rui, Zhao, Xing-Qi, Qin, Jian-Qiang, Yu, Bin, Yang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827759/
https://www.ncbi.nlm.nih.gov/pubmed/36255001
http://dx.doi.org/10.4103/1673-5374.355817
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author Qin, Han-Jun
Li, Hang
Chen, Jun-Ze
Zhang, Kai-Rui
Zhao, Xing-Qi
Qin, Jian-Qiang
Yu, Bin
Yang, Jun
author_facet Qin, Han-Jun
Li, Hang
Chen, Jun-Ze
Zhang, Kai-Rui
Zhao, Xing-Qi
Qin, Jian-Qiang
Yu, Bin
Yang, Jun
author_sort Qin, Han-Jun
collection PubMed
description Studies have shown that human hair keratin (HHK) has no antigenicity and excellent mechanical properties. Schwann cells, as unique glial cells in the peripheral nervous system, can be induced by interleukin-1β to secrete nerve growth factor, which promotes neural regeneration. Therefore, HHK with Schwann cells may be a more effective approach to repair nerve defects than HHK without Schwann cells. In this study, we established an artificial nerve graft by loading an HHK skeleton with activated Schwann cells. We found that the longitudinal HHK microfilament structure provided adhesion medium, space and direction for Schwann cells, and promoted Schwann cell growth and nerve fiber regeneration. In addition, interleukin-1β not only activates Schwann cells, but also strengthens their activity and increases the expression of nerve growth factors. Activated Schwann cells activate macrophages, and activated macrophages secrete interleukin-1β, which maintains the activity of Schwann cells. Thus, a beneficial cycle forms and promotes nerve repair. Furthermore, our studies have found that the newly constructed artificial nerve graft promotes the improvements in nerve conduction function and motor function in rats with sciatic nerve injury, and increases the expression of nerve injury repair factors fibroblast growth factor 2 and human transforming growth factor B receptor 2. These findings suggest that this artificial nerve graft effectively repairs peripheral nerve injury.
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spelling pubmed-98277592023-01-10 Artificial nerve graft constructed by coculture of activated Schwann cells and human hair keratin for repair of peripheral nerve defects Qin, Han-Jun Li, Hang Chen, Jun-Ze Zhang, Kai-Rui Zhao, Xing-Qi Qin, Jian-Qiang Yu, Bin Yang, Jun Neural Regen Res Research Article Studies have shown that human hair keratin (HHK) has no antigenicity and excellent mechanical properties. Schwann cells, as unique glial cells in the peripheral nervous system, can be induced by interleukin-1β to secrete nerve growth factor, which promotes neural regeneration. Therefore, HHK with Schwann cells may be a more effective approach to repair nerve defects than HHK without Schwann cells. In this study, we established an artificial nerve graft by loading an HHK skeleton with activated Schwann cells. We found that the longitudinal HHK microfilament structure provided adhesion medium, space and direction for Schwann cells, and promoted Schwann cell growth and nerve fiber regeneration. In addition, interleukin-1β not only activates Schwann cells, but also strengthens their activity and increases the expression of nerve growth factors. Activated Schwann cells activate macrophages, and activated macrophages secrete interleukin-1β, which maintains the activity of Schwann cells. Thus, a beneficial cycle forms and promotes nerve repair. Furthermore, our studies have found that the newly constructed artificial nerve graft promotes the improvements in nerve conduction function and motor function in rats with sciatic nerve injury, and increases the expression of nerve injury repair factors fibroblast growth factor 2 and human transforming growth factor B receptor 2. These findings suggest that this artificial nerve graft effectively repairs peripheral nerve injury. Wolters Kluwer - Medknow 2022-10-10 /pmc/articles/PMC9827759/ /pubmed/36255001 http://dx.doi.org/10.4103/1673-5374.355817 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Qin, Han-Jun
Li, Hang
Chen, Jun-Ze
Zhang, Kai-Rui
Zhao, Xing-Qi
Qin, Jian-Qiang
Yu, Bin
Yang, Jun
Artificial nerve graft constructed by coculture of activated Schwann cells and human hair keratin for repair of peripheral nerve defects
title Artificial nerve graft constructed by coculture of activated Schwann cells and human hair keratin for repair of peripheral nerve defects
title_full Artificial nerve graft constructed by coculture of activated Schwann cells and human hair keratin for repair of peripheral nerve defects
title_fullStr Artificial nerve graft constructed by coculture of activated Schwann cells and human hair keratin for repair of peripheral nerve defects
title_full_unstemmed Artificial nerve graft constructed by coculture of activated Schwann cells and human hair keratin for repair of peripheral nerve defects
title_short Artificial nerve graft constructed by coculture of activated Schwann cells and human hair keratin for repair of peripheral nerve defects
title_sort artificial nerve graft constructed by coculture of activated schwann cells and human hair keratin for repair of peripheral nerve defects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827759/
https://www.ncbi.nlm.nih.gov/pubmed/36255001
http://dx.doi.org/10.4103/1673-5374.355817
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