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Shape–motion relationships of centering microtubule asters
Although mechanisms that contribute to microtubule (MT) aster positioning have been extensively studied, still little is known on how asters move inside cells to faithfully target a cellular location. Here, we study sperm aster centration in sea urchin eggs, as a stereotypical large-scale aster move...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810306/ https://www.ncbi.nlm.nih.gov/pubmed/27022090 http://dx.doi.org/10.1083/jcb.201510064 |
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author | Tanimoto, Hirokazu Kimura, Akatsuki Minc, Nicolas |
author_facet | Tanimoto, Hirokazu Kimura, Akatsuki Minc, Nicolas |
author_sort | Tanimoto, Hirokazu |
collection | PubMed |
description | Although mechanisms that contribute to microtubule (MT) aster positioning have been extensively studied, still little is known on how asters move inside cells to faithfully target a cellular location. Here, we study sperm aster centration in sea urchin eggs, as a stereotypical large-scale aster movement with extreme constraints on centering speed and precision. By tracking three-dimensional aster centration dynamics in eggs with manipulated shapes, we show that aster geometry resulting from MT growth and interaction with cell boundaries dictates aster instantaneous directionality, yielding cell shape–dependent centering trajectories. Aster laser surgery and modeling suggest that dynein-dependent MT cytoplasmic pulling forces that scale to MT length function to convert aster geometry into directionality. In contrast, aster speed remains largely independent of aster size, shape, or absolute dynein activity, which suggests it may be predominantly determined by aster growth rate rather than MT force amplitude. These studies begin to define the geometrical principles that control aster movements. |
format | Online Article Text |
id | pubmed-4810306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48103062016-09-28 Shape–motion relationships of centering microtubule asters Tanimoto, Hirokazu Kimura, Akatsuki Minc, Nicolas J Cell Biol Research Articles Although mechanisms that contribute to microtubule (MT) aster positioning have been extensively studied, still little is known on how asters move inside cells to faithfully target a cellular location. Here, we study sperm aster centration in sea urchin eggs, as a stereotypical large-scale aster movement with extreme constraints on centering speed and precision. By tracking three-dimensional aster centration dynamics in eggs with manipulated shapes, we show that aster geometry resulting from MT growth and interaction with cell boundaries dictates aster instantaneous directionality, yielding cell shape–dependent centering trajectories. Aster laser surgery and modeling suggest that dynein-dependent MT cytoplasmic pulling forces that scale to MT length function to convert aster geometry into directionality. In contrast, aster speed remains largely independent of aster size, shape, or absolute dynein activity, which suggests it may be predominantly determined by aster growth rate rather than MT force amplitude. These studies begin to define the geometrical principles that control aster movements. The Rockefeller University Press 2016-03-28 /pmc/articles/PMC4810306/ /pubmed/27022090 http://dx.doi.org/10.1083/jcb.201510064 Text en © 2016 Tanimoto et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Tanimoto, Hirokazu Kimura, Akatsuki Minc, Nicolas Shape–motion relationships of centering microtubule asters |
title | Shape–motion relationships of centering microtubule asters |
title_full | Shape–motion relationships of centering microtubule asters |
title_fullStr | Shape–motion relationships of centering microtubule asters |
title_full_unstemmed | Shape–motion relationships of centering microtubule asters |
title_short | Shape–motion relationships of centering microtubule asters |
title_sort | shape–motion relationships of centering microtubule asters |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810306/ https://www.ncbi.nlm.nih.gov/pubmed/27022090 http://dx.doi.org/10.1083/jcb.201510064 |
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