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Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair

Central and peripheral nerve injuries can lead to permanent paralysis and organ dysfunction. In recent years, many cell and exosome implantation techniques have been developed in an attempt to restore function after nerve injury with promising but generally unsatisfactory clinical results. Clinical...

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Autores principales: Poongodi, Raju, Chen, Ying-Lun, Yang, Tao-Hsiang, Huang, Ya-Hsien, Yang, Kuender D., Lin, Hsin-Chieh, Cheng, Jen-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707664/
https://www.ncbi.nlm.nih.gov/pubmed/34948144
http://dx.doi.org/10.3390/ijms222413347
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author Poongodi, Raju
Chen, Ying-Lun
Yang, Tao-Hsiang
Huang, Ya-Hsien
Yang, Kuender D.
Lin, Hsin-Chieh
Cheng, Jen-Kun
author_facet Poongodi, Raju
Chen, Ying-Lun
Yang, Tao-Hsiang
Huang, Ya-Hsien
Yang, Kuender D.
Lin, Hsin-Chieh
Cheng, Jen-Kun
author_sort Poongodi, Raju
collection PubMed
description Central and peripheral nerve injuries can lead to permanent paralysis and organ dysfunction. In recent years, many cell and exosome implantation techniques have been developed in an attempt to restore function after nerve injury with promising but generally unsatisfactory clinical results. Clinical outcome may be enhanced by bio-scaffolds specifically fabricated to provide the appropriate three-dimensional (3D) conduit, growth-permissive substrate, and trophic factor support required for cell survival and regeneration. In rodents, these scaffolds have been shown to promote axonal regrowth and restore limb motor function following experimental spinal cord or sciatic nerve injury. Combining the appropriate cell/exosome and scaffold type may thus achieve tissue repair and regeneration with safety and efficacy sufficient for routine clinical application. In this review, we describe the efficacies of bio-scaffolds composed of various natural polysaccharides (alginate, chitin, chitosan, and hyaluronic acid), protein polymers (gelatin, collagen, silk fibroin, fibrin, and keratin), and self-assembling peptides for repair of nerve injury. In addition, we review the capacities of these constructs for supporting in vitro cell-adhesion, mechano-transduction, proliferation, and differentiation as well as the in vivo properties critical for a successful clinical outcome, including controlled degradation and re-absorption. Finally, we describe recent advances in 3D bio-printing for nerve regeneration.
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spelling pubmed-87076642021-12-25 Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair Poongodi, Raju Chen, Ying-Lun Yang, Tao-Hsiang Huang, Ya-Hsien Yang, Kuender D. Lin, Hsin-Chieh Cheng, Jen-Kun Int J Mol Sci Review Central and peripheral nerve injuries can lead to permanent paralysis and organ dysfunction. In recent years, many cell and exosome implantation techniques have been developed in an attempt to restore function after nerve injury with promising but generally unsatisfactory clinical results. Clinical outcome may be enhanced by bio-scaffolds specifically fabricated to provide the appropriate three-dimensional (3D) conduit, growth-permissive substrate, and trophic factor support required for cell survival and regeneration. In rodents, these scaffolds have been shown to promote axonal regrowth and restore limb motor function following experimental spinal cord or sciatic nerve injury. Combining the appropriate cell/exosome and scaffold type may thus achieve tissue repair and regeneration with safety and efficacy sufficient for routine clinical application. In this review, we describe the efficacies of bio-scaffolds composed of various natural polysaccharides (alginate, chitin, chitosan, and hyaluronic acid), protein polymers (gelatin, collagen, silk fibroin, fibrin, and keratin), and self-assembling peptides for repair of nerve injury. In addition, we review the capacities of these constructs for supporting in vitro cell-adhesion, mechano-transduction, proliferation, and differentiation as well as the in vivo properties critical for a successful clinical outcome, including controlled degradation and re-absorption. Finally, we describe recent advances in 3D bio-printing for nerve regeneration. MDPI 2021-12-12 /pmc/articles/PMC8707664/ /pubmed/34948144 http://dx.doi.org/10.3390/ijms222413347 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Poongodi, Raju
Chen, Ying-Lun
Yang, Tao-Hsiang
Huang, Ya-Hsien
Yang, Kuender D.
Lin, Hsin-Chieh
Cheng, Jen-Kun
Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair
title Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair
title_full Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair
title_fullStr Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair
title_full_unstemmed Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair
title_short Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair
title_sort bio-scaffolds as cell or exosome carriers for nerve injury repair
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707664/
https://www.ncbi.nlm.nih.gov/pubmed/34948144
http://dx.doi.org/10.3390/ijms222413347
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