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The Syncytial Drosophila Embryo as a Mechanically Excitable Medium
Mitosis in the early syncytial Drosophila embryo is highly correlated in space and time, as manifested in mitotic wavefronts that propagate across the embryo. In this paper we investigate the idea that the embryo can be considered a mechanically-excitable medium, and that mitotic wavefronts can be u...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813724/ https://www.ncbi.nlm.nih.gov/pubmed/24204774 http://dx.doi.org/10.1371/journal.pone.0077216 |
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author | Idema, Timon Dubuis, Julien O. Kang, Louis Manning, M. Lisa Nelson, Philip C. Lubensky, Tom C. Liu, Andrea J. |
author_facet | Idema, Timon Dubuis, Julien O. Kang, Louis Manning, M. Lisa Nelson, Philip C. Lubensky, Tom C. Liu, Andrea J. |
author_sort | Idema, Timon |
collection | PubMed |
description | Mitosis in the early syncytial Drosophila embryo is highly correlated in space and time, as manifested in mitotic wavefronts that propagate across the embryo. In this paper we investigate the idea that the embryo can be considered a mechanically-excitable medium, and that mitotic wavefronts can be understood as nonlinear wavefronts that propagate through this medium. We study the wavefronts via both image analysis of confocal microscopy videos and theoretical models. We find that the mitotic waves travel across the embryo at a well-defined speed that decreases with replication cycle. We find two markers of the wavefront in each cycle, corresponding to the onsets of metaphase and anaphase. Each of these onsets is followed by displacements of the nuclei that obey the same wavefront pattern. To understand the mitotic wavefronts theoretically we analyze wavefront propagation in excitable media. We study two classes of models, one with biochemical signaling and one with mechanical signaling. We find that the dependence of wavefront speed on cycle number is most naturally explained by mechanical signaling, and that the entire process suggests a scenario in which biochemical and mechanical signaling are coupled. |
format | Online Article Text |
id | pubmed-3813724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38137242013-11-07 The Syncytial Drosophila Embryo as a Mechanically Excitable Medium Idema, Timon Dubuis, Julien O. Kang, Louis Manning, M. Lisa Nelson, Philip C. Lubensky, Tom C. Liu, Andrea J. PLoS One Research Article Mitosis in the early syncytial Drosophila embryo is highly correlated in space and time, as manifested in mitotic wavefronts that propagate across the embryo. In this paper we investigate the idea that the embryo can be considered a mechanically-excitable medium, and that mitotic wavefronts can be understood as nonlinear wavefronts that propagate through this medium. We study the wavefronts via both image analysis of confocal microscopy videos and theoretical models. We find that the mitotic waves travel across the embryo at a well-defined speed that decreases with replication cycle. We find two markers of the wavefront in each cycle, corresponding to the onsets of metaphase and anaphase. Each of these onsets is followed by displacements of the nuclei that obey the same wavefront pattern. To understand the mitotic wavefronts theoretically we analyze wavefront propagation in excitable media. We study two classes of models, one with biochemical signaling and one with mechanical signaling. We find that the dependence of wavefront speed on cycle number is most naturally explained by mechanical signaling, and that the entire process suggests a scenario in which biochemical and mechanical signaling are coupled. Public Library of Science 2013-10-30 /pmc/articles/PMC3813724/ /pubmed/24204774 http://dx.doi.org/10.1371/journal.pone.0077216 Text en © 2013 Idema et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Idema, Timon Dubuis, Julien O. Kang, Louis Manning, M. Lisa Nelson, Philip C. Lubensky, Tom C. Liu, Andrea J. The Syncytial Drosophila Embryo as a Mechanically Excitable Medium |
title | The Syncytial Drosophila Embryo as a Mechanically Excitable Medium |
title_full | The Syncytial Drosophila Embryo as a Mechanically Excitable Medium |
title_fullStr | The Syncytial Drosophila Embryo as a Mechanically Excitable Medium |
title_full_unstemmed | The Syncytial Drosophila Embryo as a Mechanically Excitable Medium |
title_short | The Syncytial Drosophila Embryo as a Mechanically Excitable Medium |
title_sort | syncytial drosophila embryo as a mechanically excitable medium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813724/ https://www.ncbi.nlm.nih.gov/pubmed/24204774 http://dx.doi.org/10.1371/journal.pone.0077216 |
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