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ARF6 and Rab11 as intrinsic regulators of axon regeneration

Adult central nervous system (CNS) axons do not regenerate after injury because of extrinsic inhibitory factors, and a low intrinsic capacity for axon growth. Developing CNS neurons have a better regenerative ability, but lose this with maturity. This mini-review summarises recent findings which sug...

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Autores principales: Nieuwenhuis, Bart, Eva, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124649/
https://www.ncbi.nlm.nih.gov/pubmed/29772958
http://dx.doi.org/10.1080/21541248.2018.1457914
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author Nieuwenhuis, Bart
Eva, Richard
author_facet Nieuwenhuis, Bart
Eva, Richard
author_sort Nieuwenhuis, Bart
collection PubMed
description Adult central nervous system (CNS) axons do not regenerate after injury because of extrinsic inhibitory factors, and a low intrinsic capacity for axon growth. Developing CNS neurons have a better regenerative ability, but lose this with maturity. This mini-review summarises recent findings which suggest one reason for regenerative failure is the selective distribution of growth machinery away from axons as CNS neurons mature. These studies demonstrate roles for the small GTPases ARF6 and Rab11 as intrinsic regulators of polarised transport and axon regeneration. ARF6 activation prevents the axonal transport of integrins in Rab11 endosomes in mature CNS axons. Decreasing ARF6 activation permits axonal transport, and increases regenerative ability. The findings suggest new targets for promoting axon regeneration after CNS injury.
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spelling pubmed-61246492019-11-17 ARF6 and Rab11 as intrinsic regulators of axon regeneration Nieuwenhuis, Bart Eva, Richard Small GTPases Mini-Review Adult central nervous system (CNS) axons do not regenerate after injury because of extrinsic inhibitory factors, and a low intrinsic capacity for axon growth. Developing CNS neurons have a better regenerative ability, but lose this with maturity. This mini-review summarises recent findings which suggest one reason for regenerative failure is the selective distribution of growth machinery away from axons as CNS neurons mature. These studies demonstrate roles for the small GTPases ARF6 and Rab11 as intrinsic regulators of polarised transport and axon regeneration. ARF6 activation prevents the axonal transport of integrins in Rab11 endosomes in mature CNS axons. Decreasing ARF6 activation permits axonal transport, and increases regenerative ability. The findings suggest new targets for promoting axon regeneration after CNS injury. Taylor & Francis 2018-05-17 /pmc/articles/PMC6124649/ /pubmed/29772958 http://dx.doi.org/10.1080/21541248.2018.1457914 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Mini-Review
Nieuwenhuis, Bart
Eva, Richard
ARF6 and Rab11 as intrinsic regulators of axon regeneration
title ARF6 and Rab11 as intrinsic regulators of axon regeneration
title_full ARF6 and Rab11 as intrinsic regulators of axon regeneration
title_fullStr ARF6 and Rab11 as intrinsic regulators of axon regeneration
title_full_unstemmed ARF6 and Rab11 as intrinsic regulators of axon regeneration
title_short ARF6 and Rab11 as intrinsic regulators of axon regeneration
title_sort arf6 and rab11 as intrinsic regulators of axon regeneration
topic Mini-Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124649/
https://www.ncbi.nlm.nih.gov/pubmed/29772958
http://dx.doi.org/10.1080/21541248.2018.1457914
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