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Waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation
Many developing neurons transition through a multi-polar state with many competing neurites before assuming a unipolar state with one axon and multiple dendrites. Hallmarks of the multi-polar state are large fluctuations in microtubule-based transport into and outgrowth of different neurites, althou...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805541/ https://www.ncbi.nlm.nih.gov/pubmed/26836307 http://dx.doi.org/10.7554/eLife.12387 |
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author | Winans, Amy M Collins, Sean R Meyer, Tobias |
author_facet | Winans, Amy M Collins, Sean R Meyer, Tobias |
author_sort | Winans, Amy M |
collection | PubMed |
description | Many developing neurons transition through a multi-polar state with many competing neurites before assuming a unipolar state with one axon and multiple dendrites. Hallmarks of the multi-polar state are large fluctuations in microtubule-based transport into and outgrowth of different neurites, although what drives these fluctuations remains elusive. We show that actin waves, which stochastically migrate from the cell body towards neurite tips, direct microtubule-based transport during the multi-polar state. Our data argue for a mechanical control system whereby actin waves transiently widen the neurite shaft to allow increased microtubule polymerization to direct Kinesin-based transport and create bursts of neurite extension. Actin waves also require microtubule polymerization, arguing that positive feedback links these two components. We propose that actin waves create large stochastic fluctuations in microtubule-based transport and neurite outgrowth, promoting competition between neurites as they explore the environment until sufficient external cues can direct one to become the axon. DOI: http://dx.doi.org/10.7554/eLife.12387.001 |
format | Online Article Text |
id | pubmed-4805541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48055412016-03-25 Waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation Winans, Amy M Collins, Sean R Meyer, Tobias eLife Cell Biology Many developing neurons transition through a multi-polar state with many competing neurites before assuming a unipolar state with one axon and multiple dendrites. Hallmarks of the multi-polar state are large fluctuations in microtubule-based transport into and outgrowth of different neurites, although what drives these fluctuations remains elusive. We show that actin waves, which stochastically migrate from the cell body towards neurite tips, direct microtubule-based transport during the multi-polar state. Our data argue for a mechanical control system whereby actin waves transiently widen the neurite shaft to allow increased microtubule polymerization to direct Kinesin-based transport and create bursts of neurite extension. Actin waves also require microtubule polymerization, arguing that positive feedback links these two components. We propose that actin waves create large stochastic fluctuations in microtubule-based transport and neurite outgrowth, promoting competition between neurites as they explore the environment until sufficient external cues can direct one to become the axon. DOI: http://dx.doi.org/10.7554/eLife.12387.001 eLife Sciences Publications, Ltd 2016-02-02 /pmc/articles/PMC4805541/ /pubmed/26836307 http://dx.doi.org/10.7554/eLife.12387 Text en © 2016, Winans et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Winans, Amy M Collins, Sean R Meyer, Tobias Waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation |
title | Waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation |
title_full | Waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation |
title_fullStr | Waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation |
title_full_unstemmed | Waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation |
title_short | Waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation |
title_sort | waves of actin and microtubule polymerization drive microtubule-based transport and neurite growth before single axon formation |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805541/ https://www.ncbi.nlm.nih.gov/pubmed/26836307 http://dx.doi.org/10.7554/eLife.12387 |
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