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Mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-YFP-H mice

The formation of scar tissue following nerve injury has been shown to adversely affect nerve regeneration and evidence suggests that mannose-6-phosphate (M6P), a potential scar reducing agent that affects transforming growth factor (TGF)-β activation, may enhance nerve regeneration. In this study we...

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Detalles Bibliográficos
Autores principales: Harding, A.J., Christmas, C.R., Ferguson, M.W.J., Loescher, A.R., Robinson, P.P., Boissonade, F.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204175/
https://www.ncbi.nlm.nih.gov/pubmed/25173153
http://dx.doi.org/10.1016/j.neuroscience.2014.08.034
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author Harding, A.J.
Christmas, C.R.
Ferguson, M.W.J.
Loescher, A.R.
Robinson, P.P.
Boissonade, F.M.
author_facet Harding, A.J.
Christmas, C.R.
Ferguson, M.W.J.
Loescher, A.R.
Robinson, P.P.
Boissonade, F.M.
author_sort Harding, A.J.
collection PubMed
description The formation of scar tissue following nerve injury has been shown to adversely affect nerve regeneration and evidence suggests that mannose-6-phosphate (M6P), a potential scar reducing agent that affects transforming growth factor (TGF)-β activation, may enhance nerve regeneration. In this study we utilized thy-1-YFP-H mice – a transgenic strain expressing yellow fluorescent protein (YFP) within a subset of axons – to enable visual analysis of axons regenerating through a nerve graft. Using this strain of mouse we have developed analysis techniques to visualize and quantify regeneration of individual axons across the injury site following the application of either M6P or vehicle to the site of nerve injury. No significant differences were found in the proportion of axons regenerating through the graft between M6P- and vehicle-treated grafts at any point along the graft length. Maximal sprouting occurred at 1.0 mm from the proximal graft ending in both groups. The maximum change in sprouting levels for both treatment groups occurred between the graft start and 0.5-mm interval for both treatment groups. The difference between repair groups was significant at this point with a greater increase seen in the vehicle group than the M6P group. The average length of axons regenerating across the initial graft entry was significantly shorter in M6P- than in vehicle-treated grafts, indicating that they encountered less impedance. Application of M6P appears to reduce the disruption of regenerating axons and may therefore facilitate quicker recovery; this is likely to result from altered scar tissue formation in M6P grafts in the early stages of recovery. This study also establishes the usefulness of our methods of analysis using the thy-1-YFP-H mouse strain to visualize and quantify regeneration at the level of the individual axon.
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spelling pubmed-42041752014-10-27 Mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-YFP-H mice Harding, A.J. Christmas, C.R. Ferguson, M.W.J. Loescher, A.R. Robinson, P.P. Boissonade, F.M. Neuroscience Article The formation of scar tissue following nerve injury has been shown to adversely affect nerve regeneration and evidence suggests that mannose-6-phosphate (M6P), a potential scar reducing agent that affects transforming growth factor (TGF)-β activation, may enhance nerve regeneration. In this study we utilized thy-1-YFP-H mice – a transgenic strain expressing yellow fluorescent protein (YFP) within a subset of axons – to enable visual analysis of axons regenerating through a nerve graft. Using this strain of mouse we have developed analysis techniques to visualize and quantify regeneration of individual axons across the injury site following the application of either M6P or vehicle to the site of nerve injury. No significant differences were found in the proportion of axons regenerating through the graft between M6P- and vehicle-treated grafts at any point along the graft length. Maximal sprouting occurred at 1.0 mm from the proximal graft ending in both groups. The maximum change in sprouting levels for both treatment groups occurred between the graft start and 0.5-mm interval for both treatment groups. The difference between repair groups was significant at this point with a greater increase seen in the vehicle group than the M6P group. The average length of axons regenerating across the initial graft entry was significantly shorter in M6P- than in vehicle-treated grafts, indicating that they encountered less impedance. Application of M6P appears to reduce the disruption of regenerating axons and may therefore facilitate quicker recovery; this is likely to result from altered scar tissue formation in M6P grafts in the early stages of recovery. This study also establishes the usefulness of our methods of analysis using the thy-1-YFP-H mouse strain to visualize and quantify regeneration at the level of the individual axon. Elsevier Science 2014-10-24 /pmc/articles/PMC4204175/ /pubmed/25173153 http://dx.doi.org/10.1016/j.neuroscience.2014.08.034 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Article
Harding, A.J.
Christmas, C.R.
Ferguson, M.W.J.
Loescher, A.R.
Robinson, P.P.
Boissonade, F.M.
Mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-YFP-H mice
title Mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-YFP-H mice
title_full Mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-YFP-H mice
title_fullStr Mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-YFP-H mice
title_full_unstemmed Mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-YFP-H mice
title_short Mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-YFP-H mice
title_sort mannose-6-phosphate facilitates early peripheral nerve regeneration in thy-1-yfp-h mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204175/
https://www.ncbi.nlm.nih.gov/pubmed/25173153
http://dx.doi.org/10.1016/j.neuroscience.2014.08.034
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