Cargando…
Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts
During interphase of the eukaryotic cell cycle, the microtubule (MT) cytoskeleton serves as both a supportive scaffold for organelles and an arborized system of tracks for intracellular transport. At the onset of mitosis, the position of the astral MT network, specifically its center, determines the...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851858/ https://www.ncbi.nlm.nih.gov/pubmed/33026931 http://dx.doi.org/10.1091/mbc.E20-01-0088 |
_version_ | 1783645704893235200 |
---|---|
author | Sulerud, Taylor Sami, Abdullah Bashar Li, Guihe Kloxin, April Oakey, John Gatlin, Jesse |
author_facet | Sulerud, Taylor Sami, Abdullah Bashar Li, Guihe Kloxin, April Oakey, John Gatlin, Jesse |
author_sort | Sulerud, Taylor |
collection | PubMed |
description | During interphase of the eukaryotic cell cycle, the microtubule (MT) cytoskeleton serves as both a supportive scaffold for organelles and an arborized system of tracks for intracellular transport. At the onset of mitosis, the position of the astral MT network, specifically its center, determines the eventual location of the spindle apparatus and ultimately the cytokinetic furrow. Positioning of the MT aster often results in its movement to the center of a cell, even in large blastomeres hundreds of microns in diameter. This translocation requires positioning forces, yet how these forces are generated and then integrated within cells of various sizes and geometries remains an open question. Here we describe a method that combines microfluidics, hydrogels, and Xenopus laevis egg extract to investigate the mechanics of aster movement and centration. We determined that asters were able to find the center of artificial channels and annular cylinders, even when cytoplasmic dynein-dependent pulling mechanisms were inhibited. Characterization of aster movement away from V-shaped hydrogel barriers provided additional evidence for a MT-based pushing mechanism. Importantly, the distance over which this mechanism seemed to operate was longer than that predicted by radial aster growth models, agreeing with recent models of a more complex MT network architecture within the aster. |
format | Online Article Text |
id | pubmed-7851858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-78518582021-02-18 Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts Sulerud, Taylor Sami, Abdullah Bashar Li, Guihe Kloxin, April Oakey, John Gatlin, Jesse Mol Biol Cell Articles During interphase of the eukaryotic cell cycle, the microtubule (MT) cytoskeleton serves as both a supportive scaffold for organelles and an arborized system of tracks for intracellular transport. At the onset of mitosis, the position of the astral MT network, specifically its center, determines the eventual location of the spindle apparatus and ultimately the cytokinetic furrow. Positioning of the MT aster often results in its movement to the center of a cell, even in large blastomeres hundreds of microns in diameter. This translocation requires positioning forces, yet how these forces are generated and then integrated within cells of various sizes and geometries remains an open question. Here we describe a method that combines microfluidics, hydrogels, and Xenopus laevis egg extract to investigate the mechanics of aster movement and centration. We determined that asters were able to find the center of artificial channels and annular cylinders, even when cytoplasmic dynein-dependent pulling mechanisms were inhibited. Characterization of aster movement away from V-shaped hydrogel barriers provided additional evidence for a MT-based pushing mechanism. Importantly, the distance over which this mechanism seemed to operate was longer than that predicted by radial aster growth models, agreeing with recent models of a more complex MT network architecture within the aster. The American Society for Cell Biology 2020-12-01 /pmc/articles/PMC7851858/ /pubmed/33026931 http://dx.doi.org/10.1091/mbc.E20-01-0088 Text en © 2020 Sulerud et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 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. |
spellingShingle | Articles Sulerud, Taylor Sami, Abdullah Bashar Li, Guihe Kloxin, April Oakey, John Gatlin, Jesse Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts |
title | Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts |
title_full | Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts |
title_fullStr | Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts |
title_full_unstemmed | Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts |
title_short | Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts |
title_sort | microtubule-dependent pushing forces contribute to long-distance aster movement and centration in xenopus laevis egg extracts |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851858/ https://www.ncbi.nlm.nih.gov/pubmed/33026931 http://dx.doi.org/10.1091/mbc.E20-01-0088 |
work_keys_str_mv | AT sulerudtaylor microtubuledependentpushingforcescontributetolongdistanceastermovementandcentrationinxenopuslaeviseggextracts AT samiabdullahbashar microtubuledependentpushingforcescontributetolongdistanceastermovementandcentrationinxenopuslaeviseggextracts AT liguihe microtubuledependentpushingforcescontributetolongdistanceastermovementandcentrationinxenopuslaeviseggextracts AT kloxinapril microtubuledependentpushingforcescontributetolongdistanceastermovementandcentrationinxenopuslaeviseggextracts AT oakeyjohn microtubuledependentpushingforcescontributetolongdistanceastermovementandcentrationinxenopuslaeviseggextracts AT gatlinjesse microtubuledependentpushingforcescontributetolongdistanceastermovementandcentrationinxenopuslaeviseggextracts |