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Cell Patterns Emerge from Coupled Chemical and Physical Fields with Cell Proliferation Dynamics: The Arabidopsis thaliana Root as a Study System
A central issue in developmental biology is to uncover the mechanisms by which stem cells maintain their capacity to regenerate, yet at the same time produce daughter cells that differentiate and attain their ultimate fate as a functional part of a tissue or an organ. In this paper we propose that,...
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/PMC3642054/ https://www.ncbi.nlm.nih.gov/pubmed/23658505 http://dx.doi.org/10.1371/journal.pcbi.1003026 |
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author | Barrio, Rafael A. Romero-Arias, José Roberto Noguez, Marco A. Azpeitia, Eugenio Ortiz-Gutiérrez, Elizabeth Hernández-Hernández, Valeria Cortes-Poza, Yuriria Álvarez-Buylla, Elena R. |
author_facet | Barrio, Rafael A. Romero-Arias, José Roberto Noguez, Marco A. Azpeitia, Eugenio Ortiz-Gutiérrez, Elizabeth Hernández-Hernández, Valeria Cortes-Poza, Yuriria Álvarez-Buylla, Elena R. |
author_sort | Barrio, Rafael A. |
collection | PubMed |
description | A central issue in developmental biology is to uncover the mechanisms by which stem cells maintain their capacity to regenerate, yet at the same time produce daughter cells that differentiate and attain their ultimate fate as a functional part of a tissue or an organ. In this paper we propose that, during development, cells within growing organs obtain positional information from a macroscopic physical field that is produced in space while cells are proliferating. This dynamical interaction triggers and responds to chemical and genetic processes that are specific to each biological system. We chose the root apical meristem of Arabidopsis thaliana to develop our dynamical model because this system is well studied at the molecular, genetic and cellular levels and has the key traits of multicellular stem-cell niches. We built a dynamical model that couples fundamental molecular mechanisms of the cell cycle to a tension physical field and to auxin dynamics, both of which are known to play a role in root development. We perform extensive numerical calculations that allow for quantitative comparison with experimental measurements that consider the cellular patterns at the root tip. Our model recovers, as an emergent pattern, the transition from proliferative to transition and elongation domains, characteristic of stem-cell niches in multicellular organisms. In addition, we successfully predict altered cellular patterns that are expected under various applied auxin treatments or modified physical growth conditions. Our modeling platform may be extended to explicitly consider gene regulatory networks or to treat other developmental systems. |
format | Online Article Text |
id | pubmed-3642054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36420542013-05-08 Cell Patterns Emerge from Coupled Chemical and Physical Fields with Cell Proliferation Dynamics: The Arabidopsis thaliana Root as a Study System Barrio, Rafael A. Romero-Arias, José Roberto Noguez, Marco A. Azpeitia, Eugenio Ortiz-Gutiérrez, Elizabeth Hernández-Hernández, Valeria Cortes-Poza, Yuriria Álvarez-Buylla, Elena R. PLoS Comput Biol Research Article A central issue in developmental biology is to uncover the mechanisms by which stem cells maintain their capacity to regenerate, yet at the same time produce daughter cells that differentiate and attain their ultimate fate as a functional part of a tissue or an organ. In this paper we propose that, during development, cells within growing organs obtain positional information from a macroscopic physical field that is produced in space while cells are proliferating. This dynamical interaction triggers and responds to chemical and genetic processes that are specific to each biological system. We chose the root apical meristem of Arabidopsis thaliana to develop our dynamical model because this system is well studied at the molecular, genetic and cellular levels and has the key traits of multicellular stem-cell niches. We built a dynamical model that couples fundamental molecular mechanisms of the cell cycle to a tension physical field and to auxin dynamics, both of which are known to play a role in root development. We perform extensive numerical calculations that allow for quantitative comparison with experimental measurements that consider the cellular patterns at the root tip. Our model recovers, as an emergent pattern, the transition from proliferative to transition and elongation domains, characteristic of stem-cell niches in multicellular organisms. In addition, we successfully predict altered cellular patterns that are expected under various applied auxin treatments or modified physical growth conditions. Our modeling platform may be extended to explicitly consider gene regulatory networks or to treat other developmental systems. Public Library of Science 2013-05-02 /pmc/articles/PMC3642054/ /pubmed/23658505 http://dx.doi.org/10.1371/journal.pcbi.1003026 Text en © 2013 Barrio 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 Barrio, Rafael A. Romero-Arias, José Roberto Noguez, Marco A. Azpeitia, Eugenio Ortiz-Gutiérrez, Elizabeth Hernández-Hernández, Valeria Cortes-Poza, Yuriria Álvarez-Buylla, Elena R. Cell Patterns Emerge from Coupled Chemical and Physical Fields with Cell Proliferation Dynamics: The Arabidopsis thaliana Root as a Study System |
title | Cell Patterns Emerge from Coupled Chemical and Physical Fields with Cell Proliferation Dynamics: The Arabidopsis thaliana Root as a Study System |
title_full | Cell Patterns Emerge from Coupled Chemical and Physical Fields with Cell Proliferation Dynamics: The Arabidopsis thaliana Root as a Study System |
title_fullStr | Cell Patterns Emerge from Coupled Chemical and Physical Fields with Cell Proliferation Dynamics: The Arabidopsis thaliana Root as a Study System |
title_full_unstemmed | Cell Patterns Emerge from Coupled Chemical and Physical Fields with Cell Proliferation Dynamics: The Arabidopsis thaliana Root as a Study System |
title_short | Cell Patterns Emerge from Coupled Chemical and Physical Fields with Cell Proliferation Dynamics: The Arabidopsis thaliana Root as a Study System |
title_sort | cell patterns emerge from coupled chemical and physical fields with cell proliferation dynamics: the arabidopsis thaliana root as a study system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642054/ https://www.ncbi.nlm.nih.gov/pubmed/23658505 http://dx.doi.org/10.1371/journal.pcbi.1003026 |
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