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Polarity sorting of axonal microtubules: a computational study

We present a computational model to test a “polarity sorting” mechanism for microtubule (MT) organization in developing axons. We simulate the motor-based axonal transport of short MTs to test the hypothesis that immobilized cytoplasmic dynein motors transport short MTs with their plus ends leading,...

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Autores principales: Craig, Erin M., Yeung, Howard T., Rao, Anand N., Baas, Peter W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687029/
https://www.ncbi.nlm.nih.gov/pubmed/28978741
http://dx.doi.org/10.1091/mbc.E17-06-0380
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author Craig, Erin M.
Yeung, Howard T.
Rao, Anand N.
Baas, Peter W.
author_facet Craig, Erin M.
Yeung, Howard T.
Rao, Anand N.
Baas, Peter W.
author_sort Craig, Erin M.
collection PubMed
description We present a computational model to test a “polarity sorting” mechanism for microtubule (MT) organization in developing axons. We simulate the motor-based axonal transport of short MTs to test the hypothesis that immobilized cytoplasmic dynein motors transport short MTs with their plus ends leading, so “mal-oriented” MTs with minus-end-out are transported toward the cell body while “correctly” oriented MTs are transported in the anterograde direction away from the soma. We find that dynein-based transport of short MTs can explain the predominately plus-end-out polarity pattern of axonal MTs but that transient attachments of plus-end-directed motor proteins and nonmotile cross-linker proteins are needed to explain the frequent pauses and occasional reversals observed in live-cell imaging of MT transport. Static cross-linkers increase the likelihood of a stalled “tug-of-war” between retrograde and anterograde forces on the MT, providing an explanation for the frequent pauses of short MTs and the immobility of longer MTs. We predict that inhibition of the proposed static cross-linker will produce disordered transport of short MTs and increased mobility of longer MTs. We also predict that acute inhibition of cytoplasmic dynein will disrupt the polarity sorting of MTs by increasing the likelihood of “incorrect” sorting of MTs by plus-end-directed motors.
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spelling pubmed-56870292018-01-22 Polarity sorting of axonal microtubules: a computational study Craig, Erin M. Yeung, Howard T. Rao, Anand N. Baas, Peter W. Mol Biol Cell Articles We present a computational model to test a “polarity sorting” mechanism for microtubule (MT) organization in developing axons. We simulate the motor-based axonal transport of short MTs to test the hypothesis that immobilized cytoplasmic dynein motors transport short MTs with their plus ends leading, so “mal-oriented” MTs with minus-end-out are transported toward the cell body while “correctly” oriented MTs are transported in the anterograde direction away from the soma. We find that dynein-based transport of short MTs can explain the predominately plus-end-out polarity pattern of axonal MTs but that transient attachments of plus-end-directed motor proteins and nonmotile cross-linker proteins are needed to explain the frequent pauses and occasional reversals observed in live-cell imaging of MT transport. Static cross-linkers increase the likelihood of a stalled “tug-of-war” between retrograde and anterograde forces on the MT, providing an explanation for the frequent pauses of short MTs and the immobility of longer MTs. We predict that inhibition of the proposed static cross-linker will produce disordered transport of short MTs and increased mobility of longer MTs. We also predict that acute inhibition of cytoplasmic dynein will disrupt the polarity sorting of MTs by increasing the likelihood of “incorrect” sorting of MTs by plus-end-directed motors. The American Society for Cell Biology 2017-11-07 /pmc/articles/PMC5687029/ /pubmed/28978741 http://dx.doi.org/10.1091/mbc.E17-06-0380 Text en © 2017 Craig et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Craig, Erin M.
Yeung, Howard T.
Rao, Anand N.
Baas, Peter W.
Polarity sorting of axonal microtubules: a computational study
title Polarity sorting of axonal microtubules: a computational study
title_full Polarity sorting of axonal microtubules: a computational study
title_fullStr Polarity sorting of axonal microtubules: a computational study
title_full_unstemmed Polarity sorting of axonal microtubules: a computational study
title_short Polarity sorting of axonal microtubules: a computational study
title_sort polarity sorting of axonal microtubules: a computational study
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687029/
https://www.ncbi.nlm.nih.gov/pubmed/28978741
http://dx.doi.org/10.1091/mbc.E17-06-0380
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