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An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries

Peripheral nerve injuries (PNI) are caused by a range of etiologies and result in a broad spectrum of disability. While nerve autografts are the current gold standard for the reconstruction of extensive nerve damage, the limited supply of autologous nerve and complications associated with harvesting...

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Autores principales: Patel, Nitesh P., Lyon, Kristopher A., Huang, Jason H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998615/
https://www.ncbi.nlm.nih.gov/pubmed/29862995
http://dx.doi.org/10.4103/1673-5374.232458
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author Patel, Nitesh P.
Lyon, Kristopher A.
Huang, Jason H.
author_facet Patel, Nitesh P.
Lyon, Kristopher A.
Huang, Jason H.
author_sort Patel, Nitesh P.
collection PubMed
description Peripheral nerve injuries (PNI) are caused by a range of etiologies and result in a broad spectrum of disability. While nerve autografts are the current gold standard for the reconstruction of extensive nerve damage, the limited supply of autologous nerve and complications associated with harvesting nerve from a second surgical site has driven groups from multiple disciplines, including biomedical engineering, neurosurgery, plastic surgery, and orthopedic surgery, to develop a suitable or superior alternative to autografting. Over the last couple of decades, various types of scaffolds, such as acellular nerve grafts (ANGs), nerve guidance conduits, and non-nervous tissues, have been filled with Schwann cells, stem cells, and/or neurotrophic factors to develop tissue engineered nerve grafts (TENGs). Although these have shown promising effects on peripheral nerve regeneration in experimental models, the autograft has remained the gold standard for large nerve gaps. This review provides a discussion of recent advances in the development of TENGs and their efficacy in experimental models. Specifically, TENGs have been enhanced via incorporation of genetically engineered cells, methods to improve stem cell survival and differentiation, optimized delivery of neurotrophic factors via drug delivery systems (DDS), co-administration of platelet-rich plasma (PRP), and pretreatment with chondroitinase ABC (Ch-ABC). Other notable advancements include conduits that have been bioengineered to mimic native nerve structure via cell-derived extracellular matrix (ECM) deposition, and the development of transplantable living nervous tissue constructs from rat and human dorsal root ganglia (DRG) neurons. Grafts composed of non-nervous tissues, such as vein, artery, and muscle, will be briefly discussed.
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spelling pubmed-59986152018-06-29 An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries Patel, Nitesh P. Lyon, Kristopher A. Huang, Jason H. Neural Regen Res Invited Review Peripheral nerve injuries (PNI) are caused by a range of etiologies and result in a broad spectrum of disability. While nerve autografts are the current gold standard for the reconstruction of extensive nerve damage, the limited supply of autologous nerve and complications associated with harvesting nerve from a second surgical site has driven groups from multiple disciplines, including biomedical engineering, neurosurgery, plastic surgery, and orthopedic surgery, to develop a suitable or superior alternative to autografting. Over the last couple of decades, various types of scaffolds, such as acellular nerve grafts (ANGs), nerve guidance conduits, and non-nervous tissues, have been filled with Schwann cells, stem cells, and/or neurotrophic factors to develop tissue engineered nerve grafts (TENGs). Although these have shown promising effects on peripheral nerve regeneration in experimental models, the autograft has remained the gold standard for large nerve gaps. This review provides a discussion of recent advances in the development of TENGs and their efficacy in experimental models. Specifically, TENGs have been enhanced via incorporation of genetically engineered cells, methods to improve stem cell survival and differentiation, optimized delivery of neurotrophic factors via drug delivery systems (DDS), co-administration of platelet-rich plasma (PRP), and pretreatment with chondroitinase ABC (Ch-ABC). Other notable advancements include conduits that have been bioengineered to mimic native nerve structure via cell-derived extracellular matrix (ECM) deposition, and the development of transplantable living nervous tissue constructs from rat and human dorsal root ganglia (DRG) neurons. Grafts composed of non-nervous tissues, such as vein, artery, and muscle, will be briefly discussed. Medknow Publications & Media Pvt Ltd 2018-05 /pmc/articles/PMC5998615/ /pubmed/29862995 http://dx.doi.org/10.4103/1673-5374.232458 Text en Copyright: © 2018 Neural Regeneration Research http://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 Invited Review
Patel, Nitesh P.
Lyon, Kristopher A.
Huang, Jason H.
An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries
title An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries
title_full An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries
title_fullStr An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries
title_full_unstemmed An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries
title_short An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries
title_sort update–tissue engineered nerve grafts for the repair of peripheral nerve injuries
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998615/
https://www.ncbi.nlm.nih.gov/pubmed/29862995
http://dx.doi.org/10.4103/1673-5374.232458
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