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Transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell
Cell polarity is an important cellular process that cells use for various cellular functions such as asymmetric division, cell migration, and directionality determination. In asymmetric cell division, a mother cell creates multiple polarities of various proteins simultaneously within her membrane an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214518/ https://www.ncbi.nlm.nih.gov/pubmed/32198524 http://dx.doi.org/10.1007/s00285-020-01484-z |
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author | Seirin-Lee, S. Sukekawa, T. Nakahara, T. Ishii, H. Ei, S.-I. |
author_facet | Seirin-Lee, S. Sukekawa, T. Nakahara, T. Ishii, H. Ei, S.-I. |
author_sort | Seirin-Lee, S. |
collection | PubMed |
description | Cell polarity is an important cellular process that cells use for various cellular functions such as asymmetric division, cell migration, and directionality determination. In asymmetric cell division, a mother cell creates multiple polarities of various proteins simultaneously within her membrane and cytosol to generate two different daughter cells. The formation of multiple polarities in asymmetric cell division has been found to be controlled via the regulatory system by upstream polarity of the membrane to downstream polarity of the cytosol, which is involved in not only polarity establishment but also polarity positioning. However, the mechanism for polarity positioning remains unclear. In this study, we found a general mechanism and mathematical structure for the multiple streams of polarities to determine their relative position via conceptional models based on the biological example of the asymmetric cell division process of C. elegans embryo. Using conceptional modeling and model reductions, we show that the positional relation of polarities is determined by a contrasting role of regulation by upstream polarity proteins on the transition process of diffusion dynamics of downstream proteins. We analytically prove that our findings hold under the general mathematical conditions, suggesting that the mechanism of relative position between upstream and downstream dynamics could be understood without depending on a specific type of bio-chemical reaction, and it could be the universal mechanism in multiple streams of polarity dynamics of the cell. |
format | Online Article Text |
id | pubmed-7214518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-72145182020-05-14 Transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell Seirin-Lee, S. Sukekawa, T. Nakahara, T. Ishii, H. Ei, S.-I. J Math Biol Article Cell polarity is an important cellular process that cells use for various cellular functions such as asymmetric division, cell migration, and directionality determination. In asymmetric cell division, a mother cell creates multiple polarities of various proteins simultaneously within her membrane and cytosol to generate two different daughter cells. The formation of multiple polarities in asymmetric cell division has been found to be controlled via the regulatory system by upstream polarity of the membrane to downstream polarity of the cytosol, which is involved in not only polarity establishment but also polarity positioning. However, the mechanism for polarity positioning remains unclear. In this study, we found a general mechanism and mathematical structure for the multiple streams of polarities to determine their relative position via conceptional models based on the biological example of the asymmetric cell division process of C. elegans embryo. Using conceptional modeling and model reductions, we show that the positional relation of polarities is determined by a contrasting role of regulation by upstream polarity proteins on the transition process of diffusion dynamics of downstream proteins. We analytically prove that our findings hold under the general mathematical conditions, suggesting that the mechanism of relative position between upstream and downstream dynamics could be understood without depending on a specific type of bio-chemical reaction, and it could be the universal mechanism in multiple streams of polarity dynamics of the cell. Springer Berlin Heidelberg 2020-03-20 2020 /pmc/articles/PMC7214518/ /pubmed/32198524 http://dx.doi.org/10.1007/s00285-020-01484-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Seirin-Lee, S. Sukekawa, T. Nakahara, T. Ishii, H. Ei, S.-I. Transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell |
title | Transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell |
title_full | Transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell |
title_fullStr | Transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell |
title_full_unstemmed | Transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell |
title_short | Transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell |
title_sort | transitions to slow or fast diffusions provide a general property for in-phase or anti-phase polarity in a cell |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214518/ https://www.ncbi.nlm.nih.gov/pubmed/32198524 http://dx.doi.org/10.1007/s00285-020-01484-z |
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