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Production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration?

Both lyophilization and electrospinning are commonly used to make chitosan scaffolds. However, it remains unknown which method is better for cell growth. In this study, we established the following groups: (1) lyophilization group—chitosan scaffolds were prepared by lyophilization method and seeded...

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Autores principales: Wu, Yu-Xuan, Ma, Hao, Wang, Jian-Lan, Qu, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224144/
https://www.ncbi.nlm.nih.gov/pubmed/33269755
http://dx.doi.org/10.4103/1673-5374.300463
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author Wu, Yu-Xuan
Ma, Hao
Wang, Jian-Lan
Qu, Wei
author_facet Wu, Yu-Xuan
Ma, Hao
Wang, Jian-Lan
Qu, Wei
author_sort Wu, Yu-Xuan
collection PubMed
description Both lyophilization and electrospinning are commonly used to make chitosan scaffolds. However, it remains unknown which method is better for cell growth. In this study, we established the following groups: (1) lyophilization group—chitosan scaffolds were prepared by lyophilization method and seeded with Schwann cells from Sprague-Dawley rats aged 3–5 days; (2) electrospinning group—chitosan scaffolds were prepared by electrospinning method and seeded with Schwann cells; (3) control group—Schwann cells were cultured on culture dishes. The growth of Schwann cells was evaluated by immunofluorescence and scanning electron microscopy. Western blot assay was performed to explore the mechanism of Schwann cell growth. Both materials were non-toxic and suitable for the growth of Schwann cells. The pores produced by electrospinning were much smaller than those produced by lyophilization. The proliferation rate and adhesion rate of Schwann cells in the electrospinning group were higher than those in the lyophilization group. Schwann cells cultured on electrospinning scaffolds formed a Bungner band-like structure, and a much greater amount of brain-derived neurotrophic factor was secreted, which can promote the growth of neurons. Our findings show that the chitosan scaffold prepared by the electrospinning method has a nanofiber structure that provides an extracellular matrix that is more favorable for cell-cell interactions. The electrospinning method is more suitable for nerve regeneration than the lyophilization method. This research was approved by the Medical Ethical Committee of Dalian Medical University (approval No. AEE1-2016-045) on March 3, 2016.
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spelling pubmed-82241442021-07-02 Production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration? Wu, Yu-Xuan Ma, Hao Wang, Jian-Lan Qu, Wei Neural Regen Res Research Article Both lyophilization and electrospinning are commonly used to make chitosan scaffolds. However, it remains unknown which method is better for cell growth. In this study, we established the following groups: (1) lyophilization group—chitosan scaffolds were prepared by lyophilization method and seeded with Schwann cells from Sprague-Dawley rats aged 3–5 days; (2) electrospinning group—chitosan scaffolds were prepared by electrospinning method and seeded with Schwann cells; (3) control group—Schwann cells were cultured on culture dishes. The growth of Schwann cells was evaluated by immunofluorescence and scanning electron microscopy. Western blot assay was performed to explore the mechanism of Schwann cell growth. Both materials were non-toxic and suitable for the growth of Schwann cells. The pores produced by electrospinning were much smaller than those produced by lyophilization. The proliferation rate and adhesion rate of Schwann cells in the electrospinning group were higher than those in the lyophilization group. Schwann cells cultured on electrospinning scaffolds formed a Bungner band-like structure, and a much greater amount of brain-derived neurotrophic factor was secreted, which can promote the growth of neurons. Our findings show that the chitosan scaffold prepared by the electrospinning method has a nanofiber structure that provides an extracellular matrix that is more favorable for cell-cell interactions. The electrospinning method is more suitable for nerve regeneration than the lyophilization method. This research was approved by the Medical Ethical Committee of Dalian Medical University (approval No. AEE1-2016-045) on March 3, 2016. Wolters Kluwer - Medknow 2020-11-27 /pmc/articles/PMC8224144/ /pubmed/33269755 http://dx.doi.org/10.4103/1673-5374.300463 Text en Copyright: © 2021 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
Wu, Yu-Xuan
Ma, Hao
Wang, Jian-Lan
Qu, Wei
Production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration?
title Production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration?
title_full Production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration?
title_fullStr Production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration?
title_full_unstemmed Production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration?
title_short Production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration?
title_sort production of chitosan scaffolds by lyophilization or electrospinning: which is better for peripheral nerve regeneration?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224144/
https://www.ncbi.nlm.nih.gov/pubmed/33269755
http://dx.doi.org/10.4103/1673-5374.300463
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