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Axonal Transport: A Constrained System

Long-distance intracellular axonal transport is predominantly microtubule-based, and its impairment is linked to neurodegeneration. Here we review recent theoretical and experimental evidence that suggest that near the axon boundaries (walls), the effective viscosity can become large enough to imped...

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Detalles Bibliográficos
Autores principales: Yu, Clare C., Reddy, Babu J. N., Wortman, Juliana C., Gross, Steven P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245579/
https://www.ncbi.nlm.nih.gov/pubmed/30467560
http://dx.doi.org/10.29245/2572.942X/2017/3.1118
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author Yu, Clare C.
Reddy, Babu J. N.
Wortman, Juliana C.
Gross, Steven P.
author_facet Yu, Clare C.
Reddy, Babu J. N.
Wortman, Juliana C.
Gross, Steven P.
author_sort Yu, Clare C.
collection PubMed
description Long-distance intracellular axonal transport is predominantly microtubule-based, and its impairment is linked to neurodegeneration. Here we review recent theoretical and experimental evidence that suggest that near the axon boundaries (walls), the effective viscosity can become large enough to impede cargo transport in small (but not large) caliber axons. Theoretical work suggests that this opposition to motion increases rapidly as the cargo approaches the wall. However, having parallel microtubules close enough together to enable a cargo to simultaneously engage motors on more than one microtubule dramatically enhances motor activity, and thus decreases the effects due to such opposition. Experimental evidence supports this hypothesis: in small caliber axons, microtubule density is higher, increasing the probability of having parallel microtubules close enough that they can be used simultaneously by motors on a cargo. For transport toward the minus-end of microtubules, e.g., toward the cell body in an axon, a recently discovered force adaptation system can also contribute to overcoming such opposition to motion.
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spelling pubmed-62455792018-11-20 Axonal Transport: A Constrained System Yu, Clare C. Reddy, Babu J. N. Wortman, Juliana C. Gross, Steven P. J Neurol Neuromedicine Article Long-distance intracellular axonal transport is predominantly microtubule-based, and its impairment is linked to neurodegeneration. Here we review recent theoretical and experimental evidence that suggest that near the axon boundaries (walls), the effective viscosity can become large enough to impede cargo transport in small (but not large) caliber axons. Theoretical work suggests that this opposition to motion increases rapidly as the cargo approaches the wall. However, having parallel microtubules close enough together to enable a cargo to simultaneously engage motors on more than one microtubule dramatically enhances motor activity, and thus decreases the effects due to such opposition. Experimental evidence supports this hypothesis: in small caliber axons, microtubule density is higher, increasing the probability of having parallel microtubules close enough that they can be used simultaneously by motors on a cargo. For transport toward the minus-end of microtubules, e.g., toward the cell body in an axon, a recently discovered force adaptation system can also contribute to overcoming such opposition to motion. 2017-03-21 2017 /pmc/articles/PMC6245579/ /pubmed/30467560 http://dx.doi.org/10.29245/2572.942X/2017/3.1118 Text en http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 International License
spellingShingle Article
Yu, Clare C.
Reddy, Babu J. N.
Wortman, Juliana C.
Gross, Steven P.
Axonal Transport: A Constrained System
title Axonal Transport: A Constrained System
title_full Axonal Transport: A Constrained System
title_fullStr Axonal Transport: A Constrained System
title_full_unstemmed Axonal Transport: A Constrained System
title_short Axonal Transport: A Constrained System
title_sort axonal transport: a constrained system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245579/
https://www.ncbi.nlm.nih.gov/pubmed/30467560
http://dx.doi.org/10.29245/2572.942X/2017/3.1118
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