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Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs
Functional restoration following major peripheral nerve injury (PNI) is challenging, given slow axon growth rates and eventual regenerative pathway degradation in the absence of axons. We are developing tissue-engineered nerve grafts (TENGs) to simultaneously “bridge” missing nerve segments and “bab...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635828/ https://www.ncbi.nlm.nih.gov/pubmed/36332027 http://dx.doi.org/10.1126/sciadv.abm3291 |
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author | Smith, Douglas H. Burrell, Justin C. Browne, Kevin D. Katiyar, Kritika S. Ezra, Mindy I. Dutton, John L. Morand, Joseph P. Struzyna, Laura A. Laimo, Franco A. Chen, H. Isaac Wolf, John A. Kaplan, Hilton M. Rosen, Joseph M. Ledebur, Harry C. Zager, Eric L. Ali, Zarina S. Cullen, D. Kacy |
author_facet | Smith, Douglas H. Burrell, Justin C. Browne, Kevin D. Katiyar, Kritika S. Ezra, Mindy I. Dutton, John L. Morand, Joseph P. Struzyna, Laura A. Laimo, Franco A. Chen, H. Isaac Wolf, John A. Kaplan, Hilton M. Rosen, Joseph M. Ledebur, Harry C. Zager, Eric L. Ali, Zarina S. Cullen, D. Kacy |
author_sort | Smith, Douglas H. |
collection | PubMed |
description | Functional restoration following major peripheral nerve injury (PNI) is challenging, given slow axon growth rates and eventual regenerative pathway degradation in the absence of axons. We are developing tissue-engineered nerve grafts (TENGs) to simultaneously “bridge” missing nerve segments and “babysit” regenerative capacity by providing living axons to guide host axons and maintain the distal pathway. TENGs were biofabricated using porcine neurons and “stretch-grown” axon tracts. TENG neurons survived and elicited axon-facilitated axon regeneration to accelerate regrowth across both short (1 cm) and long (5 cm) segmental nerve defects in pigs. TENG axons also closely interacted with host Schwann cells to maintain proregenerative capacity. TENGs drove regeneration across 5-cm defects in both motor and mixed motor-sensory nerves, resulting in dense axon regeneration and electrophysiological recovery at levels similar to autograft repairs. This approach of accelerating axon regeneration while maintaining the pathway for long-distance regeneration may achieve recovery after currently unrepairable PNIs. |
format | Online Article Text |
id | pubmed-9635828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96358282022-11-18 Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs Smith, Douglas H. Burrell, Justin C. Browne, Kevin D. Katiyar, Kritika S. Ezra, Mindy I. Dutton, John L. Morand, Joseph P. Struzyna, Laura A. Laimo, Franco A. Chen, H. Isaac Wolf, John A. Kaplan, Hilton M. Rosen, Joseph M. Ledebur, Harry C. Zager, Eric L. Ali, Zarina S. Cullen, D. Kacy Sci Adv Biomedicine and Life Sciences Functional restoration following major peripheral nerve injury (PNI) is challenging, given slow axon growth rates and eventual regenerative pathway degradation in the absence of axons. We are developing tissue-engineered nerve grafts (TENGs) to simultaneously “bridge” missing nerve segments and “babysit” regenerative capacity by providing living axons to guide host axons and maintain the distal pathway. TENGs were biofabricated using porcine neurons and “stretch-grown” axon tracts. TENG neurons survived and elicited axon-facilitated axon regeneration to accelerate regrowth across both short (1 cm) and long (5 cm) segmental nerve defects in pigs. TENG axons also closely interacted with host Schwann cells to maintain proregenerative capacity. TENGs drove regeneration across 5-cm defects in both motor and mixed motor-sensory nerves, resulting in dense axon regeneration and electrophysiological recovery at levels similar to autograft repairs. This approach of accelerating axon regeneration while maintaining the pathway for long-distance regeneration may achieve recovery after currently unrepairable PNIs. American Association for the Advancement of Science 2022-11-04 /pmc/articles/PMC9635828/ /pubmed/36332027 http://dx.doi.org/10.1126/sciadv.abm3291 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Smith, Douglas H. Burrell, Justin C. Browne, Kevin D. Katiyar, Kritika S. Ezra, Mindy I. Dutton, John L. Morand, Joseph P. Struzyna, Laura A. Laimo, Franco A. Chen, H. Isaac Wolf, John A. Kaplan, Hilton M. Rosen, Joseph M. Ledebur, Harry C. Zager, Eric L. Ali, Zarina S. Cullen, D. Kacy Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs |
title | Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs |
title_full | Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs |
title_fullStr | Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs |
title_full_unstemmed | Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs |
title_short | Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs |
title_sort | tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635828/ https://www.ncbi.nlm.nih.gov/pubmed/36332027 http://dx.doi.org/10.1126/sciadv.abm3291 |
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