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Actin–microtubule coordination at growing microtubule ends

To power dynamic processes in cells, the actin and microtubule cytoskeletons organize into complex structures. Although it is known that cytoskeletal coordination is vital for cell function, the mechanisms by which cross-linking proteins coordinate actin and microtubule activities remain poorly unde...

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Autores principales: López, Magdalena Preciado, Huber, Florian, Grigoriev, Ilya, Steinmetz, Michel O., Akhmanova, Anna, Koenderink, Gijsje H., Dogterom, Marileen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365169/
https://www.ncbi.nlm.nih.gov/pubmed/25159196
http://dx.doi.org/10.1038/ncomms5778
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author López, Magdalena Preciado
Huber, Florian
Grigoriev, Ilya
Steinmetz, Michel O.
Akhmanova, Anna
Koenderink, Gijsje H.
Dogterom, Marileen
author_facet López, Magdalena Preciado
Huber, Florian
Grigoriev, Ilya
Steinmetz, Michel O.
Akhmanova, Anna
Koenderink, Gijsje H.
Dogterom, Marileen
author_sort López, Magdalena Preciado
collection PubMed
description To power dynamic processes in cells, the actin and microtubule cytoskeletons organize into complex structures. Although it is known that cytoskeletal coordination is vital for cell function, the mechanisms by which cross-linking proteins coordinate actin and microtubule activities remain poorly understood. In particular, it is unknown how the distinct mechanical properties of different actin architectures modulate the outcome of actin–microtubule interactions. To address this question, we engineered the protein TipAct, which links growing microtubule ends via end-binding proteins to actin filaments. We show that growing microtubules can be captured and guided by stiff actin bundles, leading to global actin–microtubule alignment. Conversely, growing microtubule ends can transport, stretch and bundle individual actin filaments, thereby globally defining actin filament organization. Our results provide a physical basis to understand actin–microtubule cross-talk, and reveal that a simple cross-linker can enable a mechanical feedback between actin and microtubule organization that is relevant to diverse biological contexts.
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spelling pubmed-43651692015-03-20 Actin–microtubule coordination at growing microtubule ends López, Magdalena Preciado Huber, Florian Grigoriev, Ilya Steinmetz, Michel O. Akhmanova, Anna Koenderink, Gijsje H. Dogterom, Marileen Nat Commun Article To power dynamic processes in cells, the actin and microtubule cytoskeletons organize into complex structures. Although it is known that cytoskeletal coordination is vital for cell function, the mechanisms by which cross-linking proteins coordinate actin and microtubule activities remain poorly understood. In particular, it is unknown how the distinct mechanical properties of different actin architectures modulate the outcome of actin–microtubule interactions. To address this question, we engineered the protein TipAct, which links growing microtubule ends via end-binding proteins to actin filaments. We show that growing microtubules can be captured and guided by stiff actin bundles, leading to global actin–microtubule alignment. Conversely, growing microtubule ends can transport, stretch and bundle individual actin filaments, thereby globally defining actin filament organization. Our results provide a physical basis to understand actin–microtubule cross-talk, and reveal that a simple cross-linker can enable a mechanical feedback between actin and microtubule organization that is relevant to diverse biological contexts. Nature Pub. Group 2014-08-27 /pmc/articles/PMC4365169/ /pubmed/25159196 http://dx.doi.org/10.1038/ncomms5778 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
López, Magdalena Preciado
Huber, Florian
Grigoriev, Ilya
Steinmetz, Michel O.
Akhmanova, Anna
Koenderink, Gijsje H.
Dogterom, Marileen
Actin–microtubule coordination at growing microtubule ends
title Actin–microtubule coordination at growing microtubule ends
title_full Actin–microtubule coordination at growing microtubule ends
title_fullStr Actin–microtubule coordination at growing microtubule ends
title_full_unstemmed Actin–microtubule coordination at growing microtubule ends
title_short Actin–microtubule coordination at growing microtubule ends
title_sort actin–microtubule coordination at growing microtubule ends
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365169/
https://www.ncbi.nlm.nih.gov/pubmed/25159196
http://dx.doi.org/10.1038/ncomms5778
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