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Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans

The capacity of an axon to regenerate is regulated by its external environment and by cell-intrinsic factors. Studies in a variety of organisms suggest that alterations in axonal microtubule (MT) dynamics have potent effects on axon regeneration. We review recent findings on the regulation of MT dyn...

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Autores principales: Tang, Ngang Heok, Chisholm, Andrew D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892358/
https://www.ncbi.nlm.nih.gov/pubmed/27350865
http://dx.doi.org/10.12688/f1000research.8197.1
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author Tang, Ngang Heok
Chisholm, Andrew D.
author_facet Tang, Ngang Heok
Chisholm, Andrew D.
author_sort Tang, Ngang Heok
collection PubMed
description The capacity of an axon to regenerate is regulated by its external environment and by cell-intrinsic factors. Studies in a variety of organisms suggest that alterations in axonal microtubule (MT) dynamics have potent effects on axon regeneration. We review recent findings on the regulation of MT dynamics during axon regeneration, focusing on the nematode Caenorhabditis elegans. In C. elegans the dual leucine zipper kinase (DLK) promotes axon regeneration, whereas the exchange factor for Arf6 (EFA-6) inhibits axon regeneration. Both DLK and EFA-6 respond to injury and control axon regeneration in part via MT dynamics. How the DLK and EFA-6 pathways are related is a topic of active investigation, as is the mechanism by which EFA-6 responds to axonal injury. We evaluate potential candidates, such as the MT affinity-regulating kinase PAR-1/MARK, in regulation of EFA-6 and axonal MT dynamics in regeneration.
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spelling pubmed-48923582016-06-03 Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans Tang, Ngang Heok Chisholm, Andrew D. F1000Res Review The capacity of an axon to regenerate is regulated by its external environment and by cell-intrinsic factors. Studies in a variety of organisms suggest that alterations in axonal microtubule (MT) dynamics have potent effects on axon regeneration. We review recent findings on the regulation of MT dynamics during axon regeneration, focusing on the nematode Caenorhabditis elegans. In C. elegans the dual leucine zipper kinase (DLK) promotes axon regeneration, whereas the exchange factor for Arf6 (EFA-6) inhibits axon regeneration. Both DLK and EFA-6 respond to injury and control axon regeneration in part via MT dynamics. How the DLK and EFA-6 pathways are related is a topic of active investigation, as is the mechanism by which EFA-6 responds to axonal injury. We evaluate potential candidates, such as the MT affinity-regulating kinase PAR-1/MARK, in regulation of EFA-6 and axonal MT dynamics in regeneration. F1000Research 2016-04-27 /pmc/articles/PMC4892358/ /pubmed/27350865 http://dx.doi.org/10.12688/f1000research.8197.1 Text en Copyright: © 2016 Tang NH and Chisholm AD http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Tang, Ngang Heok
Chisholm, Andrew D.
Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans
title Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans
title_full Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans
title_fullStr Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans
title_full_unstemmed Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans
title_short Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans
title_sort regulation of microtubule dynamics in axon regeneration: insights from c. elegans
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892358/
https://www.ncbi.nlm.nih.gov/pubmed/27350865
http://dx.doi.org/10.12688/f1000research.8197.1
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