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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2014
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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. |
format | Online Article Text |
id | pubmed-3873897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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