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Preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration

Peripheral nerve regeneration after injury is still a clinical problem. The application of autologous nerve grafting, the gold standard treatment, is greatly restricted. Acellular nerve allografts (ANAs) are considered promising alternatives, but they are difficult to achieve satisfactory therapeuti...

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Autores principales: Yu, Tianhao, Ao, Qiang, Ao, Tianrang, Ahmad, Muhammad Arslan, Wang, Aijun, Xu, Yingxi, Zhang, Zhongti, Zhou, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354778/
https://www.ncbi.nlm.nih.gov/pubmed/37476051
http://dx.doi.org/10.1002/btm2.10435
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author Yu, Tianhao
Ao, Qiang
Ao, Tianrang
Ahmad, Muhammad Arslan
Wang, Aijun
Xu, Yingxi
Zhang, Zhongti
Zhou, Qing
author_facet Yu, Tianhao
Ao, Qiang
Ao, Tianrang
Ahmad, Muhammad Arslan
Wang, Aijun
Xu, Yingxi
Zhang, Zhongti
Zhou, Qing
author_sort Yu, Tianhao
collection PubMed
description Peripheral nerve regeneration after injury is still a clinical problem. The application of autologous nerve grafting, the gold standard treatment, is greatly restricted. Acellular nerve allografts (ANAs) are considered promising alternatives, but they are difficult to achieve satisfactory therapeutic outcomes, which may be attributed to their compact inherent ultrastructure and substantial loss of extracellular matrix (ECM) components. Regarding these deficiencies, this study developed an optimized multichannel ANA by a modified decellularization method. These innovative ANAs were demonstrated to retain more ECM bioactive molecules and regenerative factors, with effective elimination of cellular antigens. The presence of microchannels with larger pore size allowed ANAs to gain higher porosity and better swelling performance, which improves their internal ultrastructure. Their mechanical properties were more similar to those of native nerves. Moreover, the optimized ANAs exhibited good biocompatibility and possessed significant advantages in supporting the proliferation and migration of Schwann cells in vitro. The in vivo results further confirmed their superior capacity to promote axon regrowth and myelination as well as restore innervation of target muscles, leading to better functional recovery than the conventional ANAs. Overall, this study demonstrates that the optimized multichannel ANAs have great potential for clinical application and offer new insight into the further improvement of ANAs.
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spelling pubmed-103547782023-07-20 Preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration Yu, Tianhao Ao, Qiang Ao, Tianrang Ahmad, Muhammad Arslan Wang, Aijun Xu, Yingxi Zhang, Zhongti Zhou, Qing Bioeng Transl Med Research Articles Peripheral nerve regeneration after injury is still a clinical problem. The application of autologous nerve grafting, the gold standard treatment, is greatly restricted. Acellular nerve allografts (ANAs) are considered promising alternatives, but they are difficult to achieve satisfactory therapeutic outcomes, which may be attributed to their compact inherent ultrastructure and substantial loss of extracellular matrix (ECM) components. Regarding these deficiencies, this study developed an optimized multichannel ANA by a modified decellularization method. These innovative ANAs were demonstrated to retain more ECM bioactive molecules and regenerative factors, with effective elimination of cellular antigens. The presence of microchannels with larger pore size allowed ANAs to gain higher porosity and better swelling performance, which improves their internal ultrastructure. Their mechanical properties were more similar to those of native nerves. Moreover, the optimized ANAs exhibited good biocompatibility and possessed significant advantages in supporting the proliferation and migration of Schwann cells in vitro. The in vivo results further confirmed their superior capacity to promote axon regrowth and myelination as well as restore innervation of target muscles, leading to better functional recovery than the conventional ANAs. Overall, this study demonstrates that the optimized multichannel ANAs have great potential for clinical application and offer new insight into the further improvement of ANAs. John Wiley & Sons, Inc. 2022-11-01 /pmc/articles/PMC10354778/ /pubmed/37476051 http://dx.doi.org/10.1002/btm2.10435 Text en © 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. 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 Research Articles
Yu, Tianhao
Ao, Qiang
Ao, Tianrang
Ahmad, Muhammad Arslan
Wang, Aijun
Xu, Yingxi
Zhang, Zhongti
Zhou, Qing
Preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration
title Preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration
title_full Preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration
title_fullStr Preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration
title_full_unstemmed Preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration
title_short Preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration
title_sort preparation and assessment of an optimized multichannel acellular nerve allograft for peripheral nerve regeneration
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354778/
https://www.ncbi.nlm.nih.gov/pubmed/37476051
http://dx.doi.org/10.1002/btm2.10435
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