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Direct observation of microtubule pushing by cortical dynein in living cells

Microtubules are under the influence of forces mediated by cytoplasmic dynein motors associated with the cell cortex. If such microtubules are free to move, they are rapidly transported inside cells. Here we directly observe fluorescent protein–labeled cortical dynein speckles and motile microtubule...

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Autores principales: Mazel, Tomáš, Biesemann, Anja, Krejczy, Magda, Nowald, Janos, Müller, Olga, Dehmelt, Leif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873897/
https://www.ncbi.nlm.nih.gov/pubmed/24173713
http://dx.doi.org/10.1091/mbc.E13-07-0376
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author Mazel, Tomáš
Biesemann, Anja
Krejczy, Magda
Nowald, Janos
Müller, Olga
Dehmelt, Leif
author_facet Mazel, Tomáš
Biesemann, Anja
Krejczy, Magda
Nowald, Janos
Müller, Olga
Dehmelt, Leif
author_sort Mazel, Tomáš
collection PubMed
description Microtubules are under the influence of forces mediated by cytoplasmic dynein motors associated with the cell cortex. If such microtubules are free to move, they are rapidly transported inside cells. Here we directly observe fluorescent protein–labeled cortical dynein speckles and motile microtubules. We find that several dynein complex subunits, including the heavy chain, the intermediate chain, and the associated dynactin subunit Dctn1 (also known as p150glued) form spatially resolved, dynamic speckles at the cell cortex, which are preferentially associated with microtubules. Measurements of bleaching and dissociation kinetics at the cell cortex reveal that these speckles often contain multiple labeled dynein heavy-chain molecules and turn over rapidly within seconds. The dynamic behavior of microtubules, such as directional movement, bending, or rotation, is influenced by association with dynein speckles, suggesting a direct physical and functional interaction. Our results support a model in which rapid turnover of cell cortex–associated dynein complexes facilitates their search to efficiently capture and push microtubules directionally with leading plus ends.
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spelling pubmed-38738972014-03-16 Direct observation of microtubule pushing by cortical dynein in living cells Mazel, Tomáš Biesemann, Anja Krejczy, Magda Nowald, Janos Müller, Olga Dehmelt, Leif Mol Biol Cell Articles Microtubules are under the influence of forces mediated by cytoplasmic dynein motors associated with the cell cortex. If such microtubules are free to move, they are rapidly transported inside cells. Here we directly observe fluorescent protein–labeled cortical dynein speckles and motile microtubules. We find that several dynein complex subunits, including the heavy chain, the intermediate chain, and the associated dynactin subunit Dctn1 (also known as p150glued) form spatially resolved, dynamic speckles at the cell cortex, which are preferentially associated with microtubules. Measurements of bleaching and dissociation kinetics at the cell cortex reveal that these speckles often contain multiple labeled dynein heavy-chain molecules and turn over rapidly within seconds. The dynamic behavior of microtubules, such as directional movement, bending, or rotation, is influenced by association with dynein speckles, suggesting a direct physical and functional interaction. Our results support a model in which rapid turnover of cell cortex–associated dynein complexes facilitates their search to efficiently capture and push microtubules directionally with leading plus ends. The American Society for Cell Biology 2014-01-01 /pmc/articles/PMC3873897/ /pubmed/24173713 http://dx.doi.org/10.1091/mbc.E13-07-0376 Text en © 2014 Mazel 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 of Cell Biology.
spellingShingle Articles
Mazel, Tomáš
Biesemann, Anja
Krejczy, Magda
Nowald, Janos
Müller, Olga
Dehmelt, Leif
Direct observation of microtubule pushing by cortical dynein in living cells
title Direct observation of microtubule pushing by cortical dynein in living cells
title_full Direct observation of microtubule pushing by cortical dynein in living cells
title_fullStr Direct observation of microtubule pushing by cortical dynein in living cells
title_full_unstemmed Direct observation of microtubule pushing by cortical dynein in living cells
title_short Direct observation of microtubule pushing by cortical dynein in living cells
title_sort direct observation of microtubule pushing by cortical dynein in living cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873897/
https://www.ncbi.nlm.nih.gov/pubmed/24173713
http://dx.doi.org/10.1091/mbc.E13-07-0376
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