Cargando…
The Dynamic Localization of Cytoplasmic Dynein in Neurons Is Driven by Kinesin-1
Cytoplasmic dynein, the major motor driving retrograde axonal transport, must be actively localized to axon terminals. This localization is critical as dynein powers essential retrograde trafficking events required for neuronal survival, such as neurotrophic signaling. Here, we demonstrate that the...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893161/ https://www.ncbi.nlm.nih.gov/pubmed/27210554 http://dx.doi.org/10.1016/j.neuron.2016.04.046 |
_version_ | 1782435507307806720 |
---|---|
author | Twelvetrees, Alison E. Pernigo, Stefano Sanger, Anneri Guedes-Dias, Pedro Schiavo, Giampietro Steiner, Roberto A. Dodding, Mark P. Holzbaur, Erika L.F. |
author_facet | Twelvetrees, Alison E. Pernigo, Stefano Sanger, Anneri Guedes-Dias, Pedro Schiavo, Giampietro Steiner, Roberto A. Dodding, Mark P. Holzbaur, Erika L.F. |
author_sort | Twelvetrees, Alison E. |
collection | PubMed |
description | Cytoplasmic dynein, the major motor driving retrograde axonal transport, must be actively localized to axon terminals. This localization is critical as dynein powers essential retrograde trafficking events required for neuronal survival, such as neurotrophic signaling. Here, we demonstrate that the outward transport of dynein from soma to axon terminal is driven by direct interactions with the anterograde motor kinesin-1. In developing neurons, we find that dynein dynamically cycles between neurites, following kinesin-1 and accumulating in the nascent axon coincident with axon specification. In established axons, dynein is constantly transported down the axon at slow axonal transport speeds; inhibition of the kinesin-1-dynein interaction effectively blocks this process. In vitro and live-imaging assays to investigate the underlying mechanism lead us to propose a new model for the slow axonal transport of cytosolic cargos, based on short-lived direct interactions of cargo with a highly processive anterograde motor. VIDEO ABSTRACT: |
format | Online Article Text |
id | pubmed-4893161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48931612016-06-13 The Dynamic Localization of Cytoplasmic Dynein in Neurons Is Driven by Kinesin-1 Twelvetrees, Alison E. Pernigo, Stefano Sanger, Anneri Guedes-Dias, Pedro Schiavo, Giampietro Steiner, Roberto A. Dodding, Mark P. Holzbaur, Erika L.F. Neuron Article Cytoplasmic dynein, the major motor driving retrograde axonal transport, must be actively localized to axon terminals. This localization is critical as dynein powers essential retrograde trafficking events required for neuronal survival, such as neurotrophic signaling. Here, we demonstrate that the outward transport of dynein from soma to axon terminal is driven by direct interactions with the anterograde motor kinesin-1. In developing neurons, we find that dynein dynamically cycles between neurites, following kinesin-1 and accumulating in the nascent axon coincident with axon specification. In established axons, dynein is constantly transported down the axon at slow axonal transport speeds; inhibition of the kinesin-1-dynein interaction effectively blocks this process. In vitro and live-imaging assays to investigate the underlying mechanism lead us to propose a new model for the slow axonal transport of cytosolic cargos, based on short-lived direct interactions of cargo with a highly processive anterograde motor. VIDEO ABSTRACT: Cell Press 2016-06-01 /pmc/articles/PMC4893161/ /pubmed/27210554 http://dx.doi.org/10.1016/j.neuron.2016.04.046 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Twelvetrees, Alison E. Pernigo, Stefano Sanger, Anneri Guedes-Dias, Pedro Schiavo, Giampietro Steiner, Roberto A. Dodding, Mark P. Holzbaur, Erika L.F. The Dynamic Localization of Cytoplasmic Dynein in Neurons Is Driven by Kinesin-1 |
title | The Dynamic Localization of Cytoplasmic Dynein in Neurons Is Driven by Kinesin-1 |
title_full | The Dynamic Localization of Cytoplasmic Dynein in Neurons Is Driven by Kinesin-1 |
title_fullStr | The Dynamic Localization of Cytoplasmic Dynein in Neurons Is Driven by Kinesin-1 |
title_full_unstemmed | The Dynamic Localization of Cytoplasmic Dynein in Neurons Is Driven by Kinesin-1 |
title_short | The Dynamic Localization of Cytoplasmic Dynein in Neurons Is Driven by Kinesin-1 |
title_sort | dynamic localization of cytoplasmic dynein in neurons is driven by kinesin-1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893161/ https://www.ncbi.nlm.nih.gov/pubmed/27210554 http://dx.doi.org/10.1016/j.neuron.2016.04.046 |
work_keys_str_mv | AT twelvetreesalisone thedynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT pernigostefano thedynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT sangeranneri thedynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT guedesdiaspedro thedynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT schiavogiampietro thedynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT steinerrobertoa thedynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT doddingmarkp thedynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT holzbaurerikalf thedynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT twelvetreesalisone dynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT pernigostefano dynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT sangeranneri dynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT guedesdiaspedro dynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT schiavogiampietro dynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT steinerrobertoa dynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT doddingmarkp dynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 AT holzbaurerikalf dynamiclocalizationofcytoplasmicdyneininneuronsisdrivenbykinesin1 |