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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...

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Autores principales: Idema, Timon, Dubuis, Julien O., Kang, Louis, Manning, M. Lisa, Nelson, Philip C., Lubensky, Tom C., Liu, Andrea J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
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.
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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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