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Spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells
We investigate the dynamics of cell shape and analyze the actin and myosin distributions of cells exhibiting cortical density traveling waves. These waves propagate by repeated cycles of cortical compression (folding) and dilation (unfolding) that lead to periodic protrusions (oscillations) of the c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529805/ https://www.ncbi.nlm.nih.gov/pubmed/26147497 http://dx.doi.org/10.1002/cm.21229 |
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author | Driscoll, Meghan K. Losert, Wolfgang Jacobson, Ken Kapustina, Maryna |
author_facet | Driscoll, Meghan K. Losert, Wolfgang Jacobson, Ken Kapustina, Maryna |
author_sort | Driscoll, Meghan K. |
collection | PubMed |
description | We investigate the dynamics of cell shape and analyze the actin and myosin distributions of cells exhibiting cortical density traveling waves. These waves propagate by repeated cycles of cortical compression (folding) and dilation (unfolding) that lead to periodic protrusions (oscillations) of the cell boundary. The focus of our detailed analysis is the remarkable periodicity of this phenotype, in which both the overall shape transformation and distribution of actomyosin density are repeated from cycle to cycle even though the characteristics of the shape transformation vary significantly for different regions of the cell. We show, using correlation analysis, that during traveling wave propagation cortical actin and plasma membrane densities are tightly coupled at each point along the cell periphery. We also demonstrate that the major protrusion appears at the wave trailing edge just after the actin cortex density has reached a maximum. Making use of the extraordinary periodicity, we employ latrunculin to demonstrate that sequestering actin monomers can have two distinct effects: low latrunculin concentrations can trigger and enhance traveling waves but higher concentrations of this drug retard the waves. The fundamental mechanism underlying this periodically protruding phenotype, involving folding and unfolding of the cortex‐membrane couple, is likely to hold important clues for diverse phenomena including cell division and amoeboid‐type migration. © 2015 The Authors. Cytoskeleton Published by Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-4529805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45298052016-06-01 Spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells Driscoll, Meghan K. Losert, Wolfgang Jacobson, Ken Kapustina, Maryna Cytoskeleton (Hoboken) Research Articles We investigate the dynamics of cell shape and analyze the actin and myosin distributions of cells exhibiting cortical density traveling waves. These waves propagate by repeated cycles of cortical compression (folding) and dilation (unfolding) that lead to periodic protrusions (oscillations) of the cell boundary. The focus of our detailed analysis is the remarkable periodicity of this phenotype, in which both the overall shape transformation and distribution of actomyosin density are repeated from cycle to cycle even though the characteristics of the shape transformation vary significantly for different regions of the cell. We show, using correlation analysis, that during traveling wave propagation cortical actin and plasma membrane densities are tightly coupled at each point along the cell periphery. We also demonstrate that the major protrusion appears at the wave trailing edge just after the actin cortex density has reached a maximum. Making use of the extraordinary periodicity, we employ latrunculin to demonstrate that sequestering actin monomers can have two distinct effects: low latrunculin concentrations can trigger and enhance traveling waves but higher concentrations of this drug retard the waves. The fundamental mechanism underlying this periodically protruding phenotype, involving folding and unfolding of the cortex‐membrane couple, is likely to hold important clues for diverse phenomena including cell division and amoeboid‐type migration. © 2015 The Authors. Cytoskeleton Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2015-08-06 2015-06 /pmc/articles/PMC4529805/ /pubmed/26147497 http://dx.doi.org/10.1002/cm.21229 Text en © 2015 The Authors. Cytoskeleton Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/3.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Driscoll, Meghan K. Losert, Wolfgang Jacobson, Ken Kapustina, Maryna Spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells |
title | Spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells |
title_full | Spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells |
title_fullStr | Spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells |
title_full_unstemmed | Spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells |
title_short | Spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells |
title_sort | spatiotemporal relationships between the cell shape and the actomyosin cortex of periodically protruding cells |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529805/ https://www.ncbi.nlm.nih.gov/pubmed/26147497 http://dx.doi.org/10.1002/cm.21229 |
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