TY - JOUR
T1 - Bayesian Inference of Forces Causing Cytoplasmic Streaming in Caenorhabditis elegans Embryos and Mouse Oocytes
AU - Niwayama, Ritsuya
AU - Nagao, Hiromichi
AU - Kitajima, Tomoya S.
AU - Hufnagel, Lars
AU - Shinohara, Kyosuke
AU - Higuchi, Tomoyuki
AU - Ishikawa, Takuji
AU - Kimura, Akatsuki
N1 - Funding Information:
Research Organization of Information and Systems, Japan, and by JSPS/MEXT KAKENHI Grant Numbers 15KT0083, 15H04372, and 16H00816. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Funding Information:
We thank Drs. Takashi Hiiragi (EMBL, Germany) and Hiroshi Hamada (Osaka University, Japan) for supporting this study; and Dr. Jean-Léon Maître (EMBL, Germany) and members of the Cell Architecture Laboratory and Office for Research Development at the National Institute of Genetics for helpful discussions. Strains were provided by the Caenorhabditis Genetics Center, which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440). R.N. was a Research Fellow of the Japan Society for the Promotion of Science. L.H. acknowledges support from European Molecular Biology Laboratory and the Center of Modeling and Simulation in the Biosciences (BIOMS) of the University of Heidelberg. This study was carried out under the Institute of Statistical Mathematics General Cooperative Research 1 (25-GCR1-1001). This study was supported by Transdisciplinary Research Integration Center, Research Organization of Information and Systems, and MEXT/JSPS KAKENHI Grant Numbers 22– 3126, 15H04372, 15KT0083, and 16H00816.
Funding Information:
RN was a Research Fellow of the Japan Society for the Promotion of Science, and was supported by JSPS KAKENHI Grant Number 22-3126. LH acknowledges support from European Molecular Biology Laboratory and the Center of Modeling and Simulation in the Biosciences (BIOMS) of the University of Heidelberg. AK was supported by the Institute of Statistical Mathematics General Cooperative Research 1 (25-GCR1-1001), by the Transdisciplinary Research Integration Center of the Research Organization of Information and Systems, Japan, and by JSPS/MEXT KAKENHI Grant Numbers 15KT0083, 15H04372, and 16H00816. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank Drs. Takashi Hiiragi (EMBL, Germany) and Hiroshi Hamada (Osaka University, Japan) for supporting this study; and Dr. Jean-L?on Ma?tre (EMBL, Germany) and members of the Cell Architecture Laboratory and Office for Research Development at the National Institute of Genetics for helpful discussions. Strains were provided by the Caenorhabditis Genetics Center, which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440). R.N. was a Research Fellow of the Japan Society for the Promotion of Science. L.H. acknowledges support from European Molecular Biology Laboratory and the Center of Modeling and Simulation in the Biosciences (BIOMS) of the University of Heidelberg. This study was carried out under the Institute of Statistical Mathematics General Cooperative Research 1 (25-GCR1-1001). This study was supported by Transdisciplinary Research Integration Center, Research Organization of Information and Systems, and MEXT/JSPS KAKENHI Grant Numbers 22?3126, 15H04372, 15KT0083, and 16H00816.
Funding Information:
Funding: RN was a Research Fellow of the Japan Society for the Promotion of Science, and was supported by JSPS KAKENHI Grant Number 22-3126. LH acknowledges support from European Molecular Biology Laboratory and the Center of Modeling and Simulation in the Biosciences (BIOMS) of the University of Heidelberg. AK was supported by the Institute of Statistical Mathematics General Cooperative Research 1 (25-GCR1-1001), by the Transdisciplinary Research Integration Center of the
Publisher Copyright:
© 2016 Niwayama et al. 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 credited.
PY - 2016/7
Y1 - 2016/7
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85021152093&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85021152093&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0159917
DO - 10.1371/journal.pone.0159917
M3 - Article
C2 - 27472658
AN - SCOPUS:85021152093
SN - 1932-6203
VL - 11
JO - PLoS ONE
JF - PLoS ONE
IS - 7
M1 - e0159917
ER -