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Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes

Cellular structures are hydrodynamically interconnected, such that force generation in one location can move distal structures. One example of this phenomenon is cytoplasmic streaming, whereby active forces at the cell cortex induce streaming of the entire cytoplasm. However, it is not known how the...

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Autores principales: Niwayama, Ritsuya, Nagao, Hiromichi, Kitajima, Tomoya S., Hufnagel, Lars, Shinohara, Kyosuke, Higuchi, Tomoyuki, Ishikawa, Takuji, Kimura, Akatsuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966953/
https://www.ncbi.nlm.nih.gov/pubmed/27472658
http://dx.doi.org/10.1371/journal.pone.0159917
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author Niwayama, Ritsuya
Nagao, Hiromichi
Kitajima, Tomoya S.
Hufnagel, Lars
Shinohara, Kyosuke
Higuchi, Tomoyuki
Ishikawa, Takuji
Kimura, Akatsuki
author_facet Niwayama, Ritsuya
Nagao, Hiromichi
Kitajima, Tomoya S.
Hufnagel, Lars
Shinohara, Kyosuke
Higuchi, Tomoyuki
Ishikawa, Takuji
Kimura, Akatsuki
author_sort Niwayama, Ritsuya
collection PubMed
description Cellular structures are hydrodynamically interconnected, such that force generation in one location can move distal structures. One example of this phenomenon is cytoplasmic streaming, whereby active forces at the cell cortex induce streaming of the entire cytoplasm. However, it is not known how the spatial distribution and magnitude of these forces move distant objects within the cell. To address this issue, we developed a computational method that used cytoplasm hydrodynamics to infer the spatial distribution of shear stress at the cell cortex induced by active force generators from experimentally obtained flow field of cytoplasmic streaming. By applying this method, we determined the shear-stress distribution that quantitatively reproduces in vivo flow fields in Caenorhabditis elegans embryos and mouse oocytes during meiosis II. Shear stress in mouse oocytes were predicted to localize to a narrower cortical region than that with a high cortical flow velocity and corresponded with the localization of the cortical actin cap. The predicted patterns of pressure gradient in both species were consistent with species-specific cytoplasmic streaming functions. The shear-stress distribution inferred by our method can contribute to the characterization of active force generation driving biological streaming.
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spelling pubmed-49669532016-08-18 Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes Niwayama, Ritsuya Nagao, Hiromichi Kitajima, Tomoya S. Hufnagel, Lars Shinohara, Kyosuke Higuchi, Tomoyuki Ishikawa, Takuji Kimura, Akatsuki PLoS One Research Article Cellular structures are hydrodynamically interconnected, such that force generation in one location can move distal structures. One example of this phenomenon is cytoplasmic streaming, whereby active forces at the cell cortex induce streaming of the entire cytoplasm. However, it is not known how the spatial distribution and magnitude of these forces move distant objects within the cell. To address this issue, we developed a computational method that used cytoplasm hydrodynamics to infer the spatial distribution of shear stress at the cell cortex induced by active force generators from experimentally obtained flow field of cytoplasmic streaming. By applying this method, we determined the shear-stress distribution that quantitatively reproduces in vivo flow fields in Caenorhabditis elegans embryos and mouse oocytes during meiosis II. Shear stress in mouse oocytes were predicted to localize to a narrower cortical region than that with a high cortical flow velocity and corresponded with the localization of the cortical actin cap. The predicted patterns of pressure gradient in both species were consistent with species-specific cytoplasmic streaming functions. The shear-stress distribution inferred by our method can contribute to the characterization of active force generation driving biological streaming. Public Library of Science 2016-07-29 /pmc/articles/PMC4966953/ /pubmed/27472658 http://dx.doi.org/10.1371/journal.pone.0159917 Text en © 2016 Niwayama 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Niwayama, Ritsuya
Nagao, Hiromichi
Kitajima, Tomoya S.
Hufnagel, Lars
Shinohara, Kyosuke
Higuchi, Tomoyuki
Ishikawa, Takuji
Kimura, Akatsuki
Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes
title Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes
title_full Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes
title_fullStr Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes
title_full_unstemmed Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes
title_short Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes
title_sort bayesian inference of forces causing cytoplasmic streaming in caenorhabditis elegans embryos and mouse oocytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966953/
https://www.ncbi.nlm.nih.gov/pubmed/27472658
http://dx.doi.org/10.1371/journal.pone.0159917
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