Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Winans, Amy M, Collins, Sean R, Meyer, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
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
_version_ 1782423154025562112
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
work_keys_str_mv AT winansamym wavesofactinandmicrotubulepolymerizationdrivemicrotubulebasedtransportandneuritegrowthbeforesingleaxonformation
AT collinsseanr wavesofactinandmicrotubulepolymerizationdrivemicrotubulebasedtransportandneuritegrowthbeforesingleaxonformation
AT meyertobias wavesofactinandmicrotubulepolymerizationdrivemicrotubulebasedtransportandneuritegrowthbeforesingleaxonformation