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Imaging axon regeneration within synthetic nerve conduits

While axons within the central nervous system (CNS) do not regenerate following injury, those in the peripheral nervous system (PNS) do, although not in a clinically satisfactory manner as only a small proportion of axons exhibit long-distance regeneration. Moreover, functional recovery is hampered...

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Autores principales: Fogli, Barbara, Corthout, Nikky, Kerstens, Axelle, Bosse, Frank, Klimaschewski, Lars, Munck, Sebastian, Schweigreiter, Rüdiger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6626049/
https://www.ncbi.nlm.nih.gov/pubmed/31300753
http://dx.doi.org/10.1038/s41598-019-46579-w
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author Fogli, Barbara
Corthout, Nikky
Kerstens, Axelle
Bosse, Frank
Klimaschewski, Lars
Munck, Sebastian
Schweigreiter, Rüdiger
author_facet Fogli, Barbara
Corthout, Nikky
Kerstens, Axelle
Bosse, Frank
Klimaschewski, Lars
Munck, Sebastian
Schweigreiter, Rüdiger
author_sort Fogli, Barbara
collection PubMed
description While axons within the central nervous system (CNS) do not regenerate following injury, those in the peripheral nervous system (PNS) do, although not in a clinically satisfactory manner as only a small proportion of axons exhibit long-distance regeneration. Moreover, functional recovery is hampered by excessive axonal sprouting and aberrant reinnervation of target tissue. In order to investigate the mechanisms governing the regrowth of axons following injury, previous studies have used lesion paradigms of peripheral nerves in rat or mouse models, and reagents or cells have been administered to the lesion site through nerve conduits, aiming to improve early-stage regeneration. Morphological analysis of such in vivo experiments has however been limited by the incompatibility of synthetic nerve conduits with existing tissue-clearing and imaging techniques. We present herein a novel experimental approach that allows high-resolution imaging of individual axons within nerve conduits, together with quantitative assessment of fiber growth. We used a GFP-expressing mouse strain in a lesion model of the sciatic nerve to describe a strategy that combines nerve clearing, chemical treatment of chitosan nerve conduits, and long working distance confocal microscopy with image processing and analysis. This novel experimental setup provides a means of documenting axon growth within the actual conduit during the critical initial stage of regeneration. This will greatly facilitate the development and evaluation of treatment regimens to improve axonal regeneration following nerve damage.
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spelling pubmed-66260492019-07-21 Imaging axon regeneration within synthetic nerve conduits Fogli, Barbara Corthout, Nikky Kerstens, Axelle Bosse, Frank Klimaschewski, Lars Munck, Sebastian Schweigreiter, Rüdiger Sci Rep Article While axons within the central nervous system (CNS) do not regenerate following injury, those in the peripheral nervous system (PNS) do, although not in a clinically satisfactory manner as only a small proportion of axons exhibit long-distance regeneration. Moreover, functional recovery is hampered by excessive axonal sprouting and aberrant reinnervation of target tissue. In order to investigate the mechanisms governing the regrowth of axons following injury, previous studies have used lesion paradigms of peripheral nerves in rat or mouse models, and reagents or cells have been administered to the lesion site through nerve conduits, aiming to improve early-stage regeneration. Morphological analysis of such in vivo experiments has however been limited by the incompatibility of synthetic nerve conduits with existing tissue-clearing and imaging techniques. We present herein a novel experimental approach that allows high-resolution imaging of individual axons within nerve conduits, together with quantitative assessment of fiber growth. We used a GFP-expressing mouse strain in a lesion model of the sciatic nerve to describe a strategy that combines nerve clearing, chemical treatment of chitosan nerve conduits, and long working distance confocal microscopy with image processing and analysis. This novel experimental setup provides a means of documenting axon growth within the actual conduit during the critical initial stage of regeneration. This will greatly facilitate the development and evaluation of treatment regimens to improve axonal regeneration following nerve damage. Nature Publishing Group UK 2019-07-12 /pmc/articles/PMC6626049/ /pubmed/31300753 http://dx.doi.org/10.1038/s41598-019-46579-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fogli, Barbara
Corthout, Nikky
Kerstens, Axelle
Bosse, Frank
Klimaschewski, Lars
Munck, Sebastian
Schweigreiter, Rüdiger
Imaging axon regeneration within synthetic nerve conduits
title Imaging axon regeneration within synthetic nerve conduits
title_full Imaging axon regeneration within synthetic nerve conduits
title_fullStr Imaging axon regeneration within synthetic nerve conduits
title_full_unstemmed Imaging axon regeneration within synthetic nerve conduits
title_short Imaging axon regeneration within synthetic nerve conduits
title_sort imaging axon regeneration within synthetic nerve conduits
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6626049/
https://www.ncbi.nlm.nih.gov/pubmed/31300753
http://dx.doi.org/10.1038/s41598-019-46579-w
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